Variant report

Variant	rs3757869
Chromosome Location	chr7:100493998-100493999
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr7:100493860-100494010	SAEC	small airway:	n/a	n/a
2	USF1	chr7:100493580-100494000	K562	blood:	n/a	chr7:100493755-100493766
3	BHLHE40	chr7:100493664-100494277	K562	blood:	n/a	n/a
4	TBL1XR1	chr7:100493658-100494091	K562	blood:	n/a	n/a
5	JUN	chr7:100493191-100496118	K562	blood:	n/a	chr7:100494328-100494341 chr7:100493521-100493530
6	TEAD4	chr7:100493666-100494337	K562	blood:	n/a	n/a
7	POLR2A	chr7:100493873-100494028	MCF-7	breast:	n/a	n/a
8	MAX	chr7:100493689-100494367	H1-hESC	embryonic stem cell:	n/a	chr7:100493756-100493765 chr7:100493755-100493766
9	CTCF	chr7:100493591-100495920	SK-N-SH	brain:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494142-100494151 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
10	MAX	chr7:100493550-100494585	ECC-1	luminal epithelium:	n/a	chr7:100493756-100493765 chr7:100493755-100493766
11	GABPA	chr7:100493590-100494380	K562	blood:	n/a	n/a
12	NR2F2	chr7:100493577-100494443	K562	blood:	n/a	n/a
13	USF1	chr7:100493640-100494045	A549	lung:	n/a	chr7:100493755-100493766
14	RCOR1	chr7:100493759-100494365	K562	blood:	n/a	n/a
15	MYC	chr7:100493631-100495749	K562	blood:	n/a	chr7:100493756-100493765 chr7:100494831-100494840 chr7:100493755-100493766
16	MAFK	chr7:100493795-100494036	K562	blood:	n/a	n/a
17	MTA3	chr7:100493734-100494322	GM12878	blood:	n/a	n/a
18	CTCF	chr7:100493860-100494010	GM12874	blood:	n/a	n/a
19	HMGN3	chr7:100492415-100495041	K562	blood:	n/a	n/a
20	CTCF	chr7:100493900-100494003	ProgFib	skin:	n/a	n/a
21	ZBTB7A	chr7:100492182-100495231	K562	blood:	n/a	n/a
22	UBTF	chr7:100492437-100494200	K562	blood:	n/a	n/a
23	PAX5	chr7:100493758-100494066	GM12878	blood:	n/a	chr7:100493930-100493948
24	POLR2A	chr7:100493562-100495029	H1-neurons	neurons:	n/a	n/a
25	EGR1	chr7:100493055-100494141	MCF-7	breast:	n/a	chr7:100493231-100493244 chr7:100493232-100493243 chr7:100493233-100493243 chr7:100493231-100493244 chr7:100493231-100493245 chr7:100493233-100493243 chr7:100493508-100493522 chr7:100493531-100493545 chr7:100493227-100493249 chr7:100493231-100493244 chr7:100493234-100493243 chr7:100493581-100493595 chr7:100493232-100493243 chr7:100493562-100493576 chr7:100493233-100493242 chr7:100493256-100493266 chr7:100493512-100493522
26	MAX	chr7:100493658-100494577	H1-hESC	embryonic stem cell:	n/a	chr7:100493756-100493765 chr7:100493755-100493766
27	MAX	chr7:100493587-100495235	K562	blood:	n/a	chr7:100493756-100493765 chr7:100494831-100494840 chr7:100493755-100493766
28	E2F6	chr7:100493618-100495225	K562	blood:	n/a	n/a
29	BACH1	chr7:100493709-100495065	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr7:100493913-100494027	GM12892	blood:	n/a	n/a
31	PAX5	chr7:100493629-100494117	GM12878	blood:	n/a	chr7:100493930-100493948
32	MAX	chr7:100493602-100494613	H1-hESC	embryonic stem cell:	n/a	chr7:100493756-100493765 chr7:100493755-100493766
33	TEAD4	chr7:100493749-100494134	H1-hESC	embryonic stem cell:	n/a	n/a
34	HDAC2	chr7:100493594-100494566	K562	blood:	n/a	n/a
35	POLR2A	chr7:100493847-100494091	MCF-7	breast:	n/a	n/a
36	ZBTB7A	chr7:100493557-100494629	K562	blood:	n/a	n/a
37	MAX	chr7:100493443-100494663	MCF-7	breast:	n/a	chr7:100493756-100493765 chr7:100493755-100493766
38	SIN3AK20	chr7:100493077-100494075	PANC-1	pancreas:	n/a	n/a
39	EBF1	chr7:100493800-100494051	GM12878	blood:	n/a	n/a
40	MAX	chr7:100493568-100496026	K562	blood:	n/a	chr7:100493756-100493765 chr7:100494831-100494840 chr7:100493755-100493766
41	HDAC2	chr7:100492345-100495320	MCF-7	breast:	n/a	n/a
42	EGR1	chr7:100492691-100494069	K562	blood:	n/a	chr7:100493231-100493244 chr7:100493232-100493243 chr7:100493233-100493243 chr7:100493231-100493244 chr7:100493231-100493245 chr7:100492856-100492869 chr7:100493233-100493243 chr7:100493508-100493522 chr7:100493531-100493545 chr7:100493227-100493249 chr7:100492860-100492870 chr7:100493231-100493244 chr7:100492743-100492756 chr7:100493234-100493243 chr7:100493581-100493595 chr7:100493232-100493243 chr7:100493562-100493576 chr7:100493233-100493242 chr7:100493256-100493266 chr7:100493512-100493522
43	RUNX3	chr7:100493711-100494011	GM12878	blood:	n/a	n/a
44	CTBP2	chr7:100493682-100494302	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr7:100493578-100495127	H1-neurons	neurons:	n/a	n/a
46	NR2F2	chr7:100493578-100494530	K562	blood:	n/a	n/a
47	USF1	chr7:100493569-100494115	ECC-1	luminal epithelium:	n/a	chr7:100493755-100493766
48	CCNT2	chr7:100492094-100495029	K562	blood:	n/a	chr7:100492742-100492751
49	HEY1	chr7:100493608-100494022	K562	blood:	n/a	n/a
50	MAX	chr7:100493569-100494574	K562	blood:	n/a	chr7:100493756-100493765 chr7:100493755-100493766

No.	Distal block	Cell Line	Cell type
1	chr7:100491420..100497264-chr7:100607951..100612175,9	K562	blood:
2	chr7:100493649..100495175-chr7:100549463..100550982,2	MCF-7	breast:
3	chr7:100491799..100497264-chr7:100607837..100612175,9	K562	blood:
4	chr7:100493490..100497118-chr7:100701265..100703603,3	K562	blood:
5	chr7:100026330..100028591-chr7:100493941..100496922,3	K562	blood:
6	chr7:100270007..100272523-chr7:100492882..100494851,2	K562	blood:
7	chr7:100492344..100495062-chr7:100726871..100729209,3	MCF-7	breast:
8	chr7:100026330..100028332-chr7:100493941..100495752,2	K562	blood:
9	chr7:100491373..100494455-chr7:100609680..100612292,3	MCF-7	breast:
10	chr7:100491924..100495059-chr7:100886100..100889819,5	MCF-7	breast:
11	chr7:100492733..100496183-chr7:100699112..100703676,5	MCF-7	breast:
12	chr7:100491458..100494589-chr7:100859109..100862606,4	MCF-7	breast:

Variant related genes	Relation type
ACHE	TF binding region
ENSG00000172354	Chromatin interaction
ENSG00000106400	Chromatin interaction
ENSG00000225946	Chromatin interaction
ENSG00000169871	Chromatin interaction
ENSG00000146834	Chromatin interaction
ENSG00000078487	Chromatin interaction
ENSG00000222636	Chromatin interaction
ENSG00000169894	Chromatin interaction
ENSG00000106397	Chromatin interaction
ENSG00000214253	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs1054391	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10953305	0.99[ASN][1000 genomes]
rs11973000	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11978697	0.81[EUR][1000 genomes]
rs12666785	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12672665	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12705097	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13225631	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13232524	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13240020	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13241786	0.85[EUR][1000 genomes]
rs15624	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1799806	0.86[EUR][1000 genomes]
rs2405973	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2405974	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2405975	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2571598	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28852509	0.88[EUR][1000 genomes]
rs2894713	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs314369	0.87[EUR][1000 genomes]
rs314375	0.88[EUR][1000 genomes]
rs314377	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs314378	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34005963	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3757870	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3757871	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3843541	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs3843542	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3847063	0.94[ASN][1000 genomes]
rs3847064	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3847068	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3931823	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4727469	0.82[ASN][1000 genomes]
rs4727470	0.82[ASN][1000 genomes]
rs4729615	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4729617	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4729619	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4729620	0.82[ASN][1000 genomes]
rs6465776	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7783543	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7798613	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7803865	0.82[ASN][1000 genomes]
rs9718841	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1829095	chr7:99814675-100494084	Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	393 gene(s)	inside rSNPs	diseases
2	nsv1020837	chr7:100313122-100508635	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
3	esv1832517	chr7:100355490-100749246	Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
4	esv2758125	chr7:100355490-100749246	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
5	esv2759547	chr7:100355490-100749246	Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
6	nsv464647	chr7:100374087-100497131	Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
7	nsv607965	chr7:100374087-100497131	Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
8	nsv1032673	chr7:100382250-100606794	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
9	nsv888799	chr7:100406144-100497131	Enhancers Bivalent Enhancer Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
10	nsv888801	chr7:100416250-100497131	Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
11	nsv464648	chr7:100422156-100518458	Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
12	nsv607966	chr7:100422156-100518458	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
13	nsv831073	chr7:100425659-100544888	Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
14	nsv888802	chr7:100484917-100495530	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
15	nsv888803	chr7:100486656-100497131	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
16	nsv888804	chr7:100486754-100494202	Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
17	nsv888805	chr7:100486754-100498057	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
18	nsv888806	chr7:100488407-100495530	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
19	nsv888807	chr7:100490077-100498057	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
20	nsv888808	chr7:100490981-100498057	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
21	nsv888809	chr7:100491451-100495530	Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
22	nsv888810	chr7:100492127-100495530	Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
23	nsv888811	chr7:100492127-100497131	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
24	nsv888812	chr7:100492127-100498057	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
25	nsv888813	chr7:100492322-100495530	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
26	nsv607969	chr7:100492357-100493998	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
27	nsv888814	chr7:100492357-100495530	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
28	nsv888815	chr7:100492357-100497131	Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
29	nsv607970	chr7:100492493-100494949	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100491800-100495000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
2	chr7:100492000-100494000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr7:100492200-100494200	Bivalent Enhancer	Spleen	Spleen
4	chr7:100492200-100495000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr7:100492400-100494000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
6	chr7:100492400-100494200	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
7	chr7:100492400-100494400	Active TSS	Psoas Muscle	Psoas
8	chr7:100492600-100495000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr7:100493000-100494600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
10	chr7:100493200-100494400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
11	chr7:100493400-100494000	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
12	chr7:100493400-100494000	Bivalent/Poised TSS	Primary mononuclear cells fromperipheralblood	Blood
13	chr7:100493400-100494000	Bivalent Enhancer	Colon Smooth Muscle	Colon
14	chr7:100493400-100494000	Enhancers	Pancreas	Pancrea
15	chr7:100493400-100494000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
16	chr7:100493400-100494200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
17	chr7:100493400-100494200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr7:100493400-100494200	Bivalent Enhancer	HUVEC	blood vessel
19	chr7:100493400-100494800	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
20	chr7:100493400-100494800	Bivalent Enhancer	HMEC	breast
21	chr7:100493400-100495200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
22	chr7:100493600-100494000	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr7:100493600-100494000	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr7:100493600-100494000	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
25	chr7:100493600-100494000	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
26	chr7:100493600-100494000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr7:100493600-100494000	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
28	chr7:100493600-100494000	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
29	chr7:100493600-100494000	Transcr. at gene 5' and 3'	Right Atrium	heart
30	chr7:100493600-100494000	Flanking Bivalent TSS/Enh	NHEK	skin
31	chr7:100493600-100494200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
32	chr7:100493600-100494200	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr7:100493600-100494200	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr7:100493600-100494200	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr7:100493600-100494200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
36	chr7:100493600-100494200	Flanking Bivalent TSS/Enh	Primary B cells from peripheral blood	blood
37	chr7:100493600-100494200	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
38	chr7:100493600-100494200	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
39	chr7:100493600-100494200	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
40	chr7:100493600-100494200	Bivalent/Poised TSS	Right Ventricle	heart
41	chr7:100493600-100494200	Flanking Bivalent TSS/Enh	GM12878-XiMat	blood
42	chr7:100493600-100494400	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
43	chr7:100493600-100494400	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
44	chr7:100493600-100494400	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
45	chr7:100493600-100494400	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
46	chr7:100493600-100494400	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
47	chr7:100493600-100494400	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
48	chr7:100493600-100494400	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
49	chr7:100493600-100494400	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
50	chr7:100493600-100494400	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 31	rectum

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