Variant report

Variant	rs6898900
Chromosome Location	chr5:37369615-37369616
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:37369538..37373129-chr5:37377393..37380859,4	MCF-7	breast:
2	chr5:37343556..37345615-chr5:37366480..37369895,3	K562	blood:
3	chr5:37349723..37351295-chr5:37369578..37371440,2	K562	blood:

Variant related genes	Relation type
ENSG00000113569	Chromatin interaction
ENSG00000082068	Chromatin interaction

Extended variants
information (count: 161 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:131)

rs_ID	r²[population]
rs10037680	1.00[EUR][1000 genomes]
rs10038414	1.00[EUR][1000 genomes]
rs10051872	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10053094	1.00[EUR][1000 genomes]
rs10053828	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10054453	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10063001	1.00[EUR][1000 genomes]
rs10067278	1.00[CEU][hapmap]
rs10067869	1.00[EUR][1000 genomes]
rs10069026	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10070367	1.00[CEU][hapmap];0.84[AMR][1000 genomes]
rs10071032	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap]
rs10072326	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap]
rs10077748	1.00[EUR][1000 genomes]
rs10077819	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10078741	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap]
rs10085007	1.00[EUR][1000 genomes]
rs10214352	1.00[EUR][1000 genomes]
rs10472286	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10473048	1.00[MEX][hapmap]
rs10491332	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs11739318	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs11742290	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs11949254	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11953538	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11955258	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs12109225	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12186464	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs12523118	1.00[EUR][1000 genomes]
rs12656455	1.00[EUR][1000 genomes]
rs13160250	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs13166616	1.00[EUR][1000 genomes]
rs13175777	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs13355660	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13359358	1.00[EUR][1000 genomes]
rs13359981	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1554969	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs16903584	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16903585	1.00[EUR][1000 genomes]
rs16903599	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs16903615	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs16903667	1.00[EUR][1000 genomes]
rs16903675	1.00[EUR][1000 genomes]
rs1973713	1.00[EUR][1000 genomes]
rs2056869	1.00[EUR][1000 genomes]
rs2142324	1.00[EUR][1000 genomes]
rs2366166	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2366172	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs2366175	1.00[EUR][1000 genomes]
rs28429963	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap]
rs28555070	1.00[EUR][1000 genomes]
rs34871356	1.00[EUR][1000 genomes]
rs4074950	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs4242249	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs4242250	1.00[EUR][1000 genomes]
rs4334908	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs4370304	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs4395662	1.00[EUR][1000 genomes]
rs4407651	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs4407652	1.00[EUR][1000 genomes]
rs4418127	1.00[EUR][1000 genomes]
rs4449561	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs4470784	1.00[EUR][1000 genomes]
rs4499858	1.00[EUR][1000 genomes]
rs4607372	1.00[EUR][1000 genomes]
rs475517	1.00[EUR][1000 genomes]
rs481834	1.00[EUR][1000 genomes]
rs4869431	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs4869432	1.00[EUR][1000 genomes]
rs4869434	1.00[EUR][1000 genomes]
rs4869506	1.00[EUR][1000 genomes]
rs4869508	1.00[EUR][1000 genomes]
rs488315	1.00[EUR][1000 genomes]
rs489123	1.00[EUR][1000 genomes]
rs563999	1.00[EUR][1000 genomes]
rs58701977	1.00[AMR][1000 genomes]
rs587641	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs59176360	1.00[EUR][1000 genomes]
rs59468995	1.00[EUR][1000 genomes]
rs596461	1.00[EUR][1000 genomes]
rs59833929	1.00[EUR][1000 genomes]
rs60063938	1.00[EUR][1000 genomes]
rs60979839	1.00[EUR][1000 genomes]
rs61154857	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs626649	1.00[EUR][1000 genomes]
rs6451316	1.00[EUR][1000 genomes]
rs6451317	0.80[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs6451318	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs671077	1.00[EUR][1000 genomes]
rs6860757	1.00[CEU][hapmap];0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6868108	1.00[CEU][hapmap]
rs6868163	1.00[EUR][1000 genomes]
rs6868843	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs6869205	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs6871254	1.00[EUR][1000 genomes]
rs6871258	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6876447	0.86[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6887309	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6888095	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs6888597	1.00[EUR][1000 genomes]
rs6892443	1.00[CEU][hapmap]
rs6893151	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6895753	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs6898035	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73068464	1.00[EUR][1000 genomes]
rs73068483	1.00[EUR][1000 genomes]
rs768220	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7702750	1.00[EUR][1000 genomes]
rs7702907	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7703638	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7703670	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7704548	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7709224	1.00[EUR][1000 genomes]
rs7712722	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7714241	1.00[EUR][1000 genomes]
rs7724308	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7724686	1.00[EUR][1000 genomes]
rs7725018	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7725049	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7727291	1.00[EUR][1000 genomes]
rs7727356	1.00[EUR][1000 genomes]
rs7728893	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7729506	1.00[EUR][1000 genomes]
rs7730242	1.00[MEX][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7732929	1.00[CEU][hapmap];0.82[YRI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7733418	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7735454	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7736469	1.00[EUR][1000 genomes]
rs8180378	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs971785	1.00[EUR][1000 genomes]
rs974432	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530226	chr5:36906377-37606367	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv534064	chr5:37054962-37586210	Active TSS Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	nsv881511	chr5:37088627-37552852	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
4	nsv597823	chr5:37111565-37430365	Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
5	nsv1026554	chr5:37112133-37734859	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
6	nsv537726	chr5:37112133-37734859	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
7	nsv1025988	chr5:37115142-37586211	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
8	nsv537727	chr5:37115142-37586211	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
9	nsv530227	chr5:37157106-37571999	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
10	nsv880839	chr5:37173930-37465126	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
11	nsv948741	chr5:37179341-37582164	Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
12	nsv949716	chr5:37179341-37967352	Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
13	nsv597824	chr5:37206621-37409579	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
14	nsv597825	chr5:37206621-37430365	Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
15	nsv880817	chr5:37239240-37465126	Weak transcription Bivalent Enhancer Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
16	nsv881492	chr5:37239240-37543121	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
17	nsv880444	chr5:37239240-37556926	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
18	nsv1015983	chr5:37240827-37666601	Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
19	nsv1021284	chr5:37264275-37630188	ZNF genes & repeats Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
20	nsv1029088	chr5:37285576-37604945	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
21	nsv597844	chr5:37287836-37567851	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
22	nsv881076	chr5:37294473-37479198	Enhancers Strong transcription Active TSS Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
23	nsv1028058	chr5:37302941-37581735	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
24	nsv537728	chr5:37302941-37581735	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
25	nsv1023871	chr5:37330018-37804744	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
26	nsv537729	chr5:37330018-37804744	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
27	nsv1028054	chr5:37331852-37586211	ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
28	nsv537730	chr5:37331852-37586211	Strong transcription Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
29	nsv1030797	chr5:37335832-37445040	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
30	nsv471012	chr5:37349895-37545998	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37337400-37370000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:37340800-37370200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:37347400-37370000	Weak transcription	Aorta	Aorta
4	chr5:37357000-37370000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:37358200-37370200	Weak transcription	Esophagus	oesophagus
6	chr5:37358400-37370200	Weak transcription	Left Ventricle	heart
7	chr5:37364600-37369800	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr5:37364600-37370400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr5:37368000-37369800	Transcr. at gene 5' and 3'	Dnd41	blood
10	chr5:37368000-37370000	Genic enhancers	Fetal Muscle Trunk	muscle
11	chr5:37368200-37369800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr5:37368200-37369800	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr5:37368200-37369800	Enhancers	Ovary	ovary
14	chr5:37368200-37370000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr5:37368200-37370200	Enhancers	Primary T cells fromperipheralblood	blood
16	chr5:37368600-37369800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
17	chr5:37368600-37370000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr5:37368800-37369800	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr5:37368800-37369800	Enhancers	Thymus	Thymus
20	chr5:37368800-37369800	Transcr. at gene 5' and 3'	K562	blood
21	chr5:37368800-37370000	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr5:37368800-37370000	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chr5:37368800-37370000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr5:37368800-37370000	Enhancers	Brain Anterior Caudate	brain
25	chr5:37368800-37370000	Flanking Active TSS	GM12878-XiMat	blood
26	chr5:37368800-37370000	Transcr. at gene 5' and 3'	Hela-S3	cervix
27	chr5:37368800-37370200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr5:37368800-37370200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr5:37368800-37370200	Flanking Active TSS	Brain Germinal Matrix	brain
30	chr5:37368800-37370200	Enhancers	Spleen	Spleen
31	chr5:37369000-37369800	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
32	chr5:37369000-37369800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
33	chr5:37369000-37369800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr5:37369000-37369800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr5:37369000-37369800	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr5:37369000-37369800	Flanking Active TSS	HMEC	breast
37	chr5:37369000-37369800	Enhancers	Osteobl	bone
38	chr5:37369000-37370000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr5:37369000-37370000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
40	chr5:37369000-37370000	Enhancers	Liver	Liver
41	chr5:37369000-37370000	Flanking Active TSS	NHDF-Ad	bronchial
42	chr5:37369000-37370200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr5:37369000-37370200	Enhancers	Primary B cells from peripheral blood	blood
44	chr5:37369000-37370200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
45	chr5:37369000-37370200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr5:37369000-37370400	Enhancers	Small Intestine	intestine
47	chr5:37369200-37369800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr5:37369200-37369800	Enhancers	Fetal Heart	heart
49	chr5:37369200-37369800	Enhancers	Fetal Intestine Large	intestine
50	chr5:37369200-37369800	Flanking Active TSS	HepG2	liver

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