Variant report

Variant	rs553165609
Chromosome Location	chr7:4923453-4923454
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	chr7:4923400-4923550	GM12872	blood:	n/a	chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923440-4923453
2	MAX	chr7:4923068-4923651	H1-hESC	embryonic stem cell:	n/a	chr7:4923127-4923137 chr7:4923549-4923559
3	SP4	chr7:4923178-4923802	H1-hESC	embryonic stem cell:	n/a	chr7:4923443-4923459 chr7:4923339-4923355 chr7:4923465-4923476 chr7:4923445-4923456 chr7:4923546-4923562 chr7:4923463-4923479 chr7:4923548-4923564 chr7:4923461-4923477
4	CTCF	chr7:4923440-4923590	NHDF-neo	bronchial:	n/a	chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923545-4923558
5	CCNT2	chr7:4922509-4923651	K562	blood:	n/a	chr7:4923466-4923475 chr7:4923590-4923599 chr7:4923551-4923560
6	CTCF	chr7:4923360-4923510	HVMF	connective:	n/a	chr7:4923440-4923453
7	CTCF	chr7:4923183-4923667	MCF-7	breast:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
8	CTCF	chr7:4923360-4923510	HAc	cerebellar:	n/a	chr7:4923440-4923453
9	YY1	chr7:4923084-4923590	SK-N-SH_RA	brain:	n/a	chr7:4923379-4923390 chr7:4923312-4923326 chr7:4923282-4923296 chr7:4923126-4923135 chr7:4923551-4923560 chr7:4923242-4923251 chr7:4923548-4923562
10	USF1	chr7:4923157-4923562	K562	blood:	n/a	chr7:4923312-4923328
11	CTCF	chr7:4923420-4923570	HCFaa	heart:	n/a	chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923545-4923558
12	CTCF	chr7:4923207-4923650	A549	lung:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
13	CTCF	chr7:4923400-4923550	GM12875	blood:	n/a	chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923440-4923453
14	EGR1	chr7:4923236-4923865	K562	blood:	n/a	chr7:4923765-4923778 chr7:4923545-4923560 chr7:4923551-4923561 chr7:4923764-4923779 chr7:4923379-4923392 chr7:4923546-4923559 chr7:4923766-4923777
15	E2F6	chr7:4922094-4923618	K562	blood:	n/a	chr7:4923242-4923251 chr7:4922864-4922878 chr7:4923414-4923429 chr7:4923252-4923263 chr7:4923551-4923560 chr7:4923446-4923455
16	CTCF	chr7:4923440-4923590	NHEK	skin:	n/a	chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923545-4923558
17	CTCF	chr7:4923440-4923590	AoAF	blood vessel:	n/a	chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923545-4923558
18	CTCF	chr7:4923380-4923530	HA-sp	spinal cord:	n/a	chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923440-4923453
19	CTCF	chr7:4923233-4923637	LNCaP	prostate:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
20	POLR2A	chr7:4921914-4923705	H1-neurons	neurons:	n/a	n/a
21	CTCF	chr7:4923420-4923570	HCPEpiC	choroid plexus:	n/a	chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923545-4923558
22	RAD21	chr7:4923370-4923646	GM12878	blood:	n/a	chr7:4923439-4923453 chr7:4923544-4923558 chr7:4923504-4923523
23	CTCF	chr7:4923400-4923550	GM12864	blood:	n/a	chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923440-4923453
24	IRF1	chr7:4923163-4923654	K562	blood:	n/a	chr7:4923341-4923355 chr7:4923465-4923479 chr7:4923550-4923564 chr7:4923445-4923459 chr7:4923609-4923623 chr7:4923589-4923603
25	MAX	chr7:4923038-4923603	SK-N-SH	brain:	n/a	chr7:4923127-4923137 chr7:4923549-4923559 chr7:4923057-4923066 chr7:4923061-4923070
26	CTCF	chr7:4923128-4923613	HepG2	liver:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
27	MAX	chr7:4923099-4923620	A549	lung:	n/a	chr7:4923127-4923137 chr7:4923549-4923559
28	CTCF	chr7:4923157-4923702	HepG2	liver:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
29	CTCF	chr7:4923400-4923550	BE2_C	brain:	n/a	chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923440-4923453
30	CTCF	chr7:4923413-4923606	GM13976	blood:	n/a	chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923545-4923558
31	CTCF	chr7:4923440-4923590	HCPEpiC	choroid plexus:	n/a	chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923545-4923558
32	USF1	chr7:4923296-4923486	HepG2	liver:	n/a	chr7:4923312-4923328
33	RAD21	chr7:4923307-4923650	A549	lung:	n/a	chr7:4923439-4923453 chr7:4923544-4923558 chr7:4923318-4923332 chr7:4923504-4923523
34	CTCF	chr7:4923206-4923649	Pancreas_OC	pancreas:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
35	CTCF	chr7:4923290-4923699	GM12878	blood:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
36	RAD21	chr7:4923088-4923681	HepG2	liver:	n/a	chr7:4923439-4923453 chr7:4923544-4923558 chr7:4923318-4923332 chr7:4923504-4923523
37	RAD21	chr7:4923210-4923679	A549	lung:	n/a	chr7:4923439-4923453 chr7:4923544-4923558 chr7:4923318-4923332 chr7:4923504-4923523
38	RAD21	chr7:4923042-4923675	K562	blood:	n/a	chr7:4923439-4923453 chr7:4923544-4923558 chr7:4923318-4923332 chr7:4923504-4923523
39	CTCF	chr7:4923107-4923710	K562	blood:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
40	CTCF	chr7:4923407-4923625	GM19240	blood:	n/a	chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923545-4923558
41	ZBTB7A	chr7:4922593-4923485	ECC-1	luminal epithelium:	n/a	chr7:4923170-4923177
42	CTCF	chr7:4923440-4923590	HBMEC	blood vessel:	n/a	chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923545-4923558
43	CTCF	chr7:4923092-4923733	K562	blood:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
44	CTCF	chr7:4923077-4923658	H1-hESC	embryonic stem cell:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
45	CTCF	chr7:4923180-4923636	Fibrobl	skin:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
46	CTCF	chr7:4923121-4923914	HCT-116	colon:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923748-4923761 chr7:4923319-4923332 chr7:4923314-4923332
47	MAX	chr7:4922990-4923751	MCF-7	breast:	n/a	chr7:4923127-4923137 chr7:4923549-4923559 chr7:4923057-4923066 chr7:4923061-4923070
48	CREB1	chr7:4923021-4923782	HepG2	liver:	n/a	n/a
49	MAZ	chr7:4923192-4923755	HepG2	liver:	n/a	chr7:4923549-4923559
50	CTCF	chr7:4923122-4923741	MCF-7	breast:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332

No.	Distal block	Cell Line	Cell type
1	chr7:4920954..4923771-chr7:5084405..5086180,2	K562	blood:
2	chr7:4869433..4870053-chr7:4923355..4923936,3	MCF-7	breast:
3	chr7:4923091..4923826-chr7:5013336..5013934,3	K562	blood:

Variant related genes	Relation type
RADIL	TF binding region
ENSG00000272968	Chromatin interaction
ENSG00000146587	Chromatin interaction
ENSG00000196204	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529538	chr7:4509189-5151503	Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv530968	chr7:4572250-5418004	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	nsv1031697	chr7:4677463-5241790	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
4	nsv538704	chr7:4677463-5241790	Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
5	nsv887378	chr7:4730535-4929721	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
6	nsv887380	chr7:4760124-4929721	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
7	nsv823994	chr7:4792385-4928328	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
8	nsv8033	chr7:4802287-5086597	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
9	nsv1022678	chr7:4810626-5113387	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
10	nsv538705	chr7:4810626-5113387	Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
11	nsv528748	chr7:4820581-5010993	Enhancers Strong transcription Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
12	nsv1021170	chr7:4831361-5058033	Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
13	nsv538706	chr7:4831361-5058033	Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
14	nsv1025467	chr7:4850447-5021443	ZNF genes & repeats Bivalent/Poised TSS Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
15	nsv605979	chr7:4854592-4944514	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
16	nsv1021999	chr7:4862082-5003190	Genic enhancers Enhancers Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
17	nsv538707	chr7:4862082-5003190	Weak transcription Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
18	nsv1033855	chr7:4862677-5069764	Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
19	nsv605980	chr7:4876057-5003373	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
20	nsv869165	chr7:4889618-5799719	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	352 gene(s)	inside rSNPs	diseases
21	nsv971151	chr7:4915196-4928162	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
22	esv3434811	chr7:4922326-4924674	Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4921600-4923600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
2	chr7:4921600-4923800	Active TSS	Aorta	Aorta
3	chr7:4921600-4923800	Active TSS	Brain Angular Gyrus	brain
4	chr7:4921800-4923600	Active TSS	Ovary	ovary
5	chr7:4921800-4923800	Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr7:4922000-4923600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr7:4922200-4923600	Bivalent Enhancer	Primary B cells from cord blood	blood
8	chr7:4922200-4923800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr7:4922400-4923600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
10	chr7:4922400-4923600	Bivalent/Poised TSS	Thymus	Thymus
11	chr7:4922400-4923800	Active TSS	Breast Myoepithelial Primary Cells	Breast
12	chr7:4922400-4923800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
13	chr7:4922600-4923600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr7:4922600-4923600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr7:4922600-4923600	Bivalent/Poised TSS	Primary mononuclear cells fromperipheralblood	Blood
16	chr7:4922600-4923800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr7:4922600-4923800	Active TSS	Fetal Brain Female	brain
18	chr7:4922600-4923800	Active TSS	HSMM	muscle
19	chr7:4922800-4923600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
20	chr7:4922800-4923600	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
21	chr7:4922800-4923600	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
22	chr7:4922800-4923800	Active TSS	ES-I3 Cell Line	embryonic stem cell
23	chr7:4922800-4923800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr7:4922800-4923800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr7:4922800-4923800	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
26	chr7:4923200-4923600	Active TSS	Primary hematopoietic stem cells short term culture	blood
27	chr7:4923200-4923600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
28	chr7:4923200-4923600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr7:4923200-4923600	Bivalent/Poised TSS	Brain Germinal Matrix	brain
30	chr7:4923200-4923800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr7:4923200-4923800	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr7:4923200-4923800	Active TSS	Cortex derived primary cultured neurospheres	brain
33	chr7:4923200-4923800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
34	chr7:4923200-4923800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
35	chr7:4923400-4923600	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
36	chr7:4923400-4923600	Bivalent Enhancer	Placenta	Placenta
37	chr7:4923400-4923800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr7:4923400-4923800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
39	chr7:4923400-4923800	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
40	chr7:4923400-4923800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
41	chr7:4923400-4923800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr7:4923400-4923800	Bivalent/Poised TSS	Colonic Mucosa	Colon
43	chr7:4923400-4923800	Enhancers	Pancreas	Pancrea
44	chr7:4923400-4923800	Enhancers	NHDF-Ad	bronchial
45	chr7:4923400-4928200	Weak transcription	Right Atrium	heart
46	chr7:4923400-4933800	Weak transcription	H9 Cell Line	embryonic stem cell

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