EnhancerDB

Chrom	Start	End	Enhancer ID	Tissues that enhancer appears	More
chr19	3617364	3617743	vista28309	VISTA

Chrom	Position	dbSNP ID	Reference Allele	Alternative Allele	id
chr19	3617187	rs10409300	G	A	5396043
chr19	3617209	rs6510764	C	T	5396044
chr19	3617247	rs571558281	C	A,T	5396045
chr19	3617248	rs537342258	G	A	5396046
chr19	3617255	rs145638137	C	T	5396047
chr19	3617276	rs186228988	C	G	5396048
chr19	3617419	rs2024131	C	A,G	5396049
chr19	3617460	rs56298926	A	G	5396050
chr19	3617493	rs144112194	G	A	5396051
chr19	3617495	rs57416953	C	A,T	5396052
chr19	3617549	rs2024132	G	A	5396053
chr19	3617576	rs572153651	G	T	5396054
chr19	3617581	rs558019152	T	C	5396055
chr19	3617597	rs577892181	C	T	5396056
chr19	3617605	rs543760533	C	T	5396057
chr19	3617624	rs559482466	T	A,G	5396058
chr19	3617629	rs551444608	C	T	5396059
chr19	3617896	rs61408904	G	A	5396060
chr19	3617906	rs11085028	A	C	5396061
chr19	3618047	rs542548478	G	A	5396062
chr19	3618067	rs56695698	C	G,T	5396063
chr19	3618125	rs140115333	C	T	5396064
chr19	3618138	rs530461851	G	A	5396065
chr19	3618209	rs546957744	G	A	5396066
chr19	3618344	rs541282933	GC	G	5396067
chr19	3618422	rs11445996	A	AG	5396068
chr19	3618422	rs142250312	AG	A	5396069
chr19	3618422	rs528266242	A	AG	5396070
chr19	3618422	rs796110390	A	AG	5396071
chr19	3618424	rs190948344	G	A,C,T	5396072
chr19	3618489	rs2041050	T	G	5396073
chr19	3618579	rs6510765	T	C	5396074
chr19	3618589	rs150262337	G	T	5396075
chr19	3618616	rs3746127	C	G,T	5396076
chr19	3618634	rs368811246	G	A	5396077
chr19	3618688	rs3746126	A	C	5396078
chr19	3618928	rs3746125	G	A	5396079
chr19	3619008	rs200853059	T	G	5396080
chr19	3619016	rs200351614	C	A,T	5396081
chr19	3619032	rs575214765	G	T	5396082
chr19	3619219	rs374916502	G	A	5396083
chr19	3619287	rs373050795	C	A	5396084
chr19	3619332	rs184595900	C	T	5396085
chr19	3619350	rs61553804	G	A,T	5396086
chr19	3619415	rs77831925	G	A	5396087
chr19	3619642	rs147523061	C	G,T	5396088
chr19	3619643	rs138387745	G	C	5396089
chr19	3619656	rs534289047	G	A	5396090
chr19	3619679	rs11883225	G	C	5396091
chr19	3619740	rs114641615	C	T	5396092
chr19	3619799	rs543918806	G	A	5396093
chr19	3619846	rs143887722	C	T	5396094
chr19	3619917	rs192869044	A	C	5396095
chr19	3619927	rs147277899	G	A	5396096
chr19	3619969	rs73920179	A	G	5396097
chr19	3619978	rs538138471	C	T	5396098
chr19	3619982	rs568423290	C	T	5396099
chr19	3619991	rs7258056	G	T	5396100
chr19	3620086	rs148707448	C	G	5396101
chr19	3620098	rs370385181	C	A,G,T	5396102
chr19	3620281	rs372707975	A	G	5396103
chr19	3620309	rs559776691	G	A,T	5396104
chr19	3620323	rs147569786	C	CG	5396105
chr19	3620323	rs532180847	C	T	5396106
chr19	3620324	rs180869159	G	A,T	5396107
chr19	3620425	rs527651891	G	A	5396108
chr19	3620444	rs150792174	C	A,T	5396109
chr19	3620488	rs539933081	T	A	5396110
chr19	3620544	rs535797602	A	G	5396111
chr19	3620606	rs73920180	A	G	5396112
chr19	3620786	rs139224809	C	T	5396113
chr19	3620899	rs150851574	CAG	C	5396114
chr19	3620899	rs60208409	CAG	C	5396115
chr19	3620939	rs561975426	C	A,G,T	5396116
chr19	3621016	rs77428959	A	C	5396117
chr19	3621031	rs570845233	G	C	5396118
chr19	3621070	rs73920181	G	A	5396119
chr19	3621090	rs535837349	G	A	5396120
chr19	3621100	rs144091769	G	A	5396121
chr19	3621164	rs146474363	G	A	5396122
chr19	3621177	rs73920182	G	A,T	5396123
chr19	3621222	rs141013245	C	A,T	5396124
chr19	3621253	rs561724101	C	A,T	5396125
chr19	3621307	rs73920184	G	A	5396126
chr19	3621524	rs181305565	A	C	5396127
chr19	3621655	rs117550170	T	C	5396128
chr19	3621664	rs145520844	C	T	5396129
chr19	3621720	rs2240505	G	A	5396130
chr19	3621784	rs578074285	G	A	5396131
chr19	3621826	rs566654317	G	A	5396132
chr19	3621832	rs148819868	G	A	5396133

EnhancerDB

Chromosome characteristics of TCF7L2[chr19:3617168-3621842]

Enhancers possibly regulated by TCF7L2[chr19:3617168-3621842]

SNP sites on TCF7L2[chr19:3617168-3621842]

Genes possibly regulated by TCF7L2[chr19:3617168-3621842]

Details of Genes

Expression level of Genes

miRNAs possibly regulated by TCF7L2[chr19:3617168-3621842]

Details of miRNAs

Expression level of miRNAs