Variant report

Variant	rs35811165
Chromosome Location	chr7:100951533-100951534
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	POLR2A	chr7:100951463-100951812	A549	lung:	n/a	n/a
2	POLR2A	chr7:100951454-100951802	GM12878	blood:	n/a	n/a
3	TAF1	chr7:100951368-100951939	H1-hESC	embryonic stem cell:	n/a	n/a
4	STAT3	chr7:100951418-100951596	MCF10A-Er-Src	breast:	n/a	chr7:100951496-100951508 chr7:100951509-100951520
5	CHD2	chr7:100951530-100951727	H1-hESC	embryonic stem cell:	n/a	n/a
6	POLR2A	chr7:100951445-100951811	K562	blood:	n/a	n/a
7	CEBPB	chr7:100951408-100951735	Hela-S3	cervix:	n/a	n/a
8	YY1	chr7:100951433-100951901	HepG2	liver:	n/a	chr7:100951525-100951534 chr7:100951496-100951510 chr7:100951610-100951622
9	POLR2A	chr7:100951366-100951767	ECC-1	luminal epithelium:	n/a	n/a
10	JUND	chr7:100951488-100951768	H1-hESC	embryonic stem cell:	n/a	n/a
11	POLR2A	chr7:100951449-100951822	K562	blood:	n/a	n/a
12	POLR2A	chr7:100951245-100951861	HCT-116	colon:	n/a	n/a
13	POLR2A	chr7:100951429-100952169	NB4	blood:	n/a	n/a
14	POLR2A	chr7:100951421-100951857	A549	lung:	n/a	n/a
15	SIN3AK20	chr7:100951296-100951904	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr7:100951426-100951840	MCF-7	breast:	n/a	n/a
17	POLR2A	chr7:100951422-100952174	HEK293	kidney:	n/a	n/a
18	YY1	chr7:100951462-100951723	ECC-1	luminal epithelium:	n/a	chr7:100951525-100951534 chr7:100951496-100951510 chr7:100951610-100951622
19	POLR2A	chr7:100951424-100951847	PANC-1	pancreas:	n/a	n/a
20	REST	chr7:100951383-100951852	A549	lung:	n/a	n/a
21	TAF1	chr7:100951321-100951991	ECC-1	luminal epithelium:	n/a	n/a
22	GTF2F1	chr7:100951465-100951765	K562	blood:	n/a	n/a
23	TAF1	chr7:100951362-100951708	ECC-1	luminal epithelium:	n/a	n/a
24	POLR2A	chr7:100951424-100951886	A549	lung:	n/a	n/a
25	MAZ	chr7:100951446-100951664	HepG2	liver:	n/a	chr7:100951499-100951509
26	HDAC2	chr7:100951433-100952003	MCF-7	breast:	n/a	n/a
27	POLR2A	chr7:100951465-100951773	HepG2	liver:	n/a	n/a
28	POLR2A	chr7:100951134-100953336	H1-hESC	embryonic stem cell:	n/a	n/a
29	E2F6	chr7:100951462-100952184	A549	lung:	n/a	chr7:100951525-100951534
30	TAF1	chr7:100951354-100951716	K562	blood:	n/a	n/a
31	POLR2A	chr7:100951446-100951820	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr7:100951390-100951829	HCT-116	colon:	n/a	n/a
33	RFX5	chr7:100951517-100951724	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr7:100951380-100951787	PANC-1	pancreas:	n/a	n/a
35	TCF12	chr7:100951271-100952217	A549	lung:	n/a	chr7:100952073-100952080
36	STAT3	chr7:100951458-100951568	MCF10A-Er-Src	breast:	n/a	chr7:100951496-100951508 chr7:100951509-100951520
37	SIN3AK20	chr7:100951481-100951729	HepG2	liver:	n/a	n/a
38	YY1	chr7:100951488-100951778	H1-hESC	embryonic stem cell:	n/a	chr7:100951525-100951534 chr7:100951496-100951510 chr7:100951610-100951622
39	TBP	chr7:100951412-100951773	Hela-S3	cervix:	n/a	n/a
40	TAF7	chr7:100951500-100951830	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr7:100951480-100951630	GM12866	blood:	n/a	n/a
42	POLR2A	chr7:100951328-100952069	K562	blood:	n/a	n/a
43	REST	chr7:100951476-100951783	A549	lung:	n/a	n/a
44	ATF2	chr7:100951217-100951858	H1-hESC	embryonic stem cell:	n/a	n/a
45	YY1	chr7:100951395-100951760	HCT-116	colon:	n/a	chr7:100951525-100951534 chr7:100951496-100951510 chr7:100951610-100951622
46	MYC	chr7:100951394-100951602	MCF10A-Er-Src	breast:	n/a	chr7:100951499-100951509
47	FOXA2	chr7:100951319-100951563	HepG2	liver:	n/a	n/a
48	SIN3AK20	chr7:100951229-100952039	MCF-7	breast:	n/a	n/a
49	TBP	chr7:100951470-100951723	HepG2	liver:	n/a	n/a
50	MAX	chr7:100951253-100952428	MCF-7	breast:	n/a	chr7:100951499-100951509

No.	Distal block	Cell Line	Cell type
1	chr7:100951106..100952099-chr8:37552941..37553786,2	HCT-116	colon:
2	chr7:100859934..100861544-chr7:100949902..100952091,2	K562	blood:
3	chr7:100950840..100954191-chr7:100963498..100966604,5	MCF-7	breast:
4	chr7:100941733..100944347-chr7:100950677..100953123,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000232445	TF binding region
ENSG00000106397	Chromatin interaction
ENSG00000106400	Chromatin interaction
ENSG00000128581	Chromatin interaction
ENSG00000183779	Chromatin interaction
ENSG00000232301	Chromatin interaction

Extended variants
information (count: 90 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs11544858	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13223799	0.93[AFR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13225720	0.91[AFR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13234919	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13235206	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13236755	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13236818	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13237170	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13240188	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13240202	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13241096	0.93[AFR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13241519	0.93[AFR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13241528	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13243964	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2410815	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2410818	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34048830	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34077348	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34169259	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34170365	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34306578	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34331244	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34434188	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34522084	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34530598	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34532455	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34541954	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34579827	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34679185	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34714336	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34761081	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34872936	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35259540	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35401614	0.99[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35427616	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35594069	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35614350	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35642062	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35653054	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35710113	0.94[AFR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35724850	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35751380	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35757856	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35785259	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35835570	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36005187	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36060097	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36079227	0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56730418	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60697114	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66621600	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66711003	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67002599	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67502950	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67562697	0.86[EUR][1000 genomes]
rs67736913	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67922522	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67927345	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs68015521	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6968925	1.00[ASN][1000 genomes]
rs6968930	1.00[ASN][1000 genomes]
rs71540926	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71557300	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71557302	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71559403	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71559404	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs71559406	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73410736	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7781222	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7791799	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs868145	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9691191	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9692578	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933653	chr7:100701931-101515782	Active TSS ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv1030604	chr7:100717732-101223465	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
3	esv2422376	chr7:100743485-101016471	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS 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	63 gene(s)	inside rSNPs	diseases
4	nsv464651	chr7:100792810-100971604	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
5	nsv607974	chr7:100792810-100971604	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
6	nsv429788	chr7:100799565-101178565	Weak transcription Strong transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
7	esv2752134	chr7:100800131-101141867	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
8	nsv831076	chr7:100828847-101011674	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
9	esv2422326	chr7:100833449-101000131	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
10	nsv607978	chr7:100861213-100971604	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
11	nsv831077	chr7:100874209-101083930	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
12	nsv1023393	chr7:100904333-101102046	Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
13	esv2752135	chr7:100932330-101135565	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	esv2752136	chr7:100932330-101143259	Genic enhancers Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
15	nsv1017098	chr7:100935631-101117541	Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
16	nsv539042	chr7:100935631-101117541	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
17	esv2752137	chr7:100938008-101135398	ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs35811165	RP11-132A1.4	cis	Esophagus Mucosa	GTEx

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100950600-100953000	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr7:100950800-100951600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr7:100950800-100952800	Active TSS	HUES6 Cell Line	embryonic stem cell
4	chr7:100950800-100952800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
5	chr7:100950800-100953200	Active TSS	H9 Cell Line	embryonic stem cell
6	chr7:100951000-100951800	Bivalent/Poised TSS	Primary T cells from cord blood	blood
7	chr7:100951000-100951800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr7:100951000-100952000	Active TSS	iPS-15b Cell Line	embryonic stem cell
9	chr7:100951000-100952000	Active TSS	Breast Myoepithelial Primary Cells	Breast
10	chr7:100951000-100952200	Active TSS	HMEC	breast
11	chr7:100951000-100952200	Active TSS	NHEK	skin
12	chr7:100951000-100952800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr7:100951000-100952800	Active TSS	HUES64 Cell Line	embryonic stem cell
14	chr7:100951000-100952800	Active TSS	iPS-18 Cell Line	embryonic stem cell
15	chr7:100951000-100952800	Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr7:100951000-100952800	Active TSS	Hela-S3	cervix
17	chr7:100951000-100953000	Active TSS	H1 Cell Line	embryonic stem cell
18	chr7:100951000-100953200	Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr7:100951200-100951600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr7:100951200-100951600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
21	chr7:100951200-100951600	Active TSS	Liver	Liver
22	chr7:100951200-100951600	Bivalent Enhancer	Placenta	Placenta
23	chr7:100951200-100951600	Bivalent Enhancer	Fetal Thymus	thymus
24	chr7:100951200-100951600	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
25	chr7:100951200-100951600	Active TSS	Right Ventricle	heart
26	chr7:100951200-100951600	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
27	chr7:100951200-100951600	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
28	chr7:100951200-100951600	Active TSS	HUVEC	blood vessel
29	chr7:100951200-100951600	Active TSS	NH-A	brain
30	chr7:100951200-100951600	Bivalent/Poised TSS	NHLF	lung
31	chr7:100951200-100951800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr7:100951200-100951800	Bivalent Enhancer	Primary hematopoietic stem cells	blood
33	chr7:100951200-100951800	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
34	chr7:100951200-100951800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr7:100951200-100951800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr7:100951200-100951800	Active TSS	Brain Anterior Caudate	brain
37	chr7:100951200-100951800	Bivalent/Poised TSS	Colonic Mucosa	Colon
38	chr7:100951200-100951800	Bivalent/Poised TSS	Fetal Brain Female	brain
39	chr7:100951200-100951800	Bivalent/Poised TSS	Fetal Intestine Small	intestine
40	chr7:100951200-100951800	Active TSS	Fetal Kidney	kidney
41	chr7:100951200-100952000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr7:100951200-100952000	Active TSS	Pancreas	Pancrea
43	chr7:100951200-100952200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr7:100951200-100952200	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr7:100951200-100952200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr7:100951200-100952200	Active TSS	Muscle Satellite Cultured Cells	--
47	chr7:100951200-100952200	Bivalent/Poised TSS	Brain Germinal Matrix	brain
48	chr7:100951200-100952200	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
49	chr7:100951200-100952200	Active TSS	Gastric	stomach
50	chr7:100951200-100952200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum

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