Variant report

Variant	rs528316495
Chromosome Location	chr7:4923650-4923651
allele	-/GGAGGGGGGGTCCCC
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	MAX	chr7:4923068-4923651	H1-hESC	embryonic stem cell:	n/a	chr7:4923127-4923137 chr7:4923549-4923559
2	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
3	CCNT2	chr7:4922509-4923651	K562	blood:	n/a	chr7:4923466-4923475 chr7:4923590-4923599 chr7:4923551-4923560
4	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
5	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
6	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
7	POLR2A	chr7:4921914-4923705	H1-neurons	neurons:	n/a	n/a
8	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
9	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
10	RAD21	chr7:4923307-4923650	A549	lung:	n/a	chr7:4923439-4923453 chr7:4923544-4923558 chr7:4923318-4923332 chr7:4923504-4923523
11	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
12	RAD21	chr7:4923088-4923681	HepG2	liver:	n/a	chr7:4923439-4923453 chr7:4923544-4923558 chr7:4923318-4923332 chr7:4923504-4923523
13	RAD21	chr7:4923210-4923679	A549	lung:	n/a	chr7:4923439-4923453 chr7:4923544-4923558 chr7:4923318-4923332 chr7:4923504-4923523
14	RAD21	chr7:4923042-4923675	K562	blood:	n/a	chr7:4923439-4923453 chr7:4923544-4923558 chr7:4923318-4923332 chr7:4923504-4923523
15	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
16	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
17	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
18	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
19	MAX	chr7:4922990-4923751	MCF-7	breast:	n/a	chr7:4923127-4923137 chr7:4923549-4923559 chr7:4923057-4923066 chr7:4923061-4923070
20	CTCF	chr7:4923520-4923670	NB4	blood:	n/a	chr7:4923542-4923560 chr7:4923545-4923558
21	CREB1	chr7:4923021-4923782	HepG2	liver:	n/a	n/a
22	MAZ	chr7:4923192-4923755	HepG2	liver:	n/a	chr7:4923549-4923559
23	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
24	MAX	chr7:4922976-4923694	HepG2	liver:	n/a	chr7:4923127-4923137 chr7:4923549-4923559 chr7:4923057-4923066 chr7:4923061-4923070
25	MAX	chr7:4922997-4923678	H1-hESC	embryonic stem cell:	n/a	chr7:4923127-4923137 chr7:4923549-4923559 chr7:4923057-4923066 chr7:4923061-4923070
26	HCFC1	chr7:4923163-4923694	K562	blood:	n/a	n/a
27	CTCF	chr7:4923178-4923658	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
28	MXI1	chr7:4921317-4924106	SK-N-SH	brain:	n/a	chr7:4923055-4923070
29	CTCF	chr7:4922936-4923720	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 chr7:4923020-4923030 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
30	TBP	chr7:4923327-4923685	HepG2	liver:	n/a	n/a
31	RAD21	chr7:4923085-4923760	MCF-7	breast:	n/a	chr7:4923439-4923453 chr7:4923544-4923558 chr7:4923318-4923332 chr7:4923504-4923523
32	EGR1	chr7:4923140-4923887	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
33	CTCF	chr7:4923540-4923690	HCM	heart:	n/a	chr7:4923542-4923560 chr7:4923545-4923558
34	ZC3H11A	chr7:4923310-4923679	K562	blood:	n/a	n/a
35	E2F6	chr7:4923099-4923726	H1-hESC	embryonic stem cell:	n/a	chr7:4923242-4923251 chr7:4923414-4923429 chr7:4923252-4923263 chr7:4923551-4923560 chr7:4923446-4923455
36	MAX	chr7:4923092-4923662	K562	blood:	n/a	chr7:4923127-4923137 chr7:4923549-4923559
37	CTCF	chr7:4923154-4923651	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
38	RAD21	chr7:4923101-4923744	ECC-1	luminal epithelium:	n/a	chr7:4923439-4923453 chr7:4923544-4923558 chr7:4923318-4923332 chr7:4923504-4923523
39	RAD21	chr7:4923155-4923805	MCF-7	breast:	n/a	chr7:4923439-4923453 chr7:4923544-4923558 chr7:4923318-4923332 chr7:4923504-4923523
40	JUND	chr7:4922930-4923698	K562	blood:	n/a	chr7:4923341-4923350
41	MAX	chr7:4922877-4923694	K562	blood:	n/a	chr7:4923127-4923137 chr7:4923549-4923559 chr7:4923057-4923066 chr7:4923061-4923070 chr7:4922912-4922921
42	RCOR1	chr7:4923034-4923696	K562	blood:	n/a	n/a
43	CTCF	chr7:4921537-4924514	SK-N-SH	brain:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4922058-4922071 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923020-4923030 chr7:4923545-4923558 chr7:4923748-4923761 chr7:4923319-4923332 chr7:4923314-4923332 chr7:4921846-4921859
44	CTCF	chr7:4922990-4923677	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 chr7:4923020-4923030 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
45	CTCF	chr7:4923212-4923651	GM19239	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
46	CTCF	chr7:4923187-4923657	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
47	MYC	chr7:4923061-4923651	K562	blood:	n/a	chr7:4923127-4923137 chr7:4923549-4923559 chr7:4923061-4923070
48	ZNF143	chr7:4923208-4923674	H1-hESC	embryonic stem cell:	n/a	n/a
49	SRF	chr7:4923239-4923719	ECC-1	luminal epithelium:	n/a	chr7:4923549-4923559 chr7:4923283-4923293 chr7:4923465-4923475 chr7:4923377-4923387
50	RAD21	chr7:4923124-4923676	SK-N-SH_RA	brain:	n/a	chr7:4923439-4923453 chr7:4923544-4923558 chr7:4923318-4923332 chr7:4923504-4923523

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4923615-4923665	AG10803	skin:	n/a
2	chr7:4923615-4923665	SK-N-SH	brain:	n/a
3	chr7:4923615-4923665	AG09319	gingival:	n/a
4	chr7:4923615-4923665	ovcar-3	ovarian:	n/a
5	chr7:4923615-4923665	SK-N-MC	brain:	n/a
6	chr7:4923615-4923665	RPTEC	kidney:	n/a
7	chr7:4923615-4923665	BE2_C	brain:	n/a
8	chr7:4923615-4923665	PANC-1	pancreas:	n/a
9	chr7:4923615-4923665	SKMC	muscle:	n/a
10	chr7:4923615-4923665	AG04450	lung:	fetal
11	chr7:4923615-4923665	H1-hESC	embryonic stem cell:	embryo
12	chr7:4923615-4923665	ProgFib	skin:	n/a
13	chr7:4923615-4923665	MCF10A-Er-Src	breast:	n/a
14	chr7:4923615-4923665	T-47D	breast:	n/a
15	chr7:4923615-4923665	HIPEpiC	eye:	n/a
16	chr7:4923615-4923665	ECC-1	luminal epithelium:	n/a
17	chr7:4923615-4923665	HCF	heart:	n/a
18	chr7:4923615-4923665	HNPCEpiC	eye:	n/a
19	chr7:4923615-4923665	LNCaP	prostate:	n/a
20	chr7:4923615-4923665	HMEC	breast:	n/a
21	chr7:4923615-4923665	GM12891	blood:	n/a
22	chr7:4923615-4923665	PrEC	prostate:	n/a
23	chr7:4923615-4923665	NHBE	bronchial:	n/a
24	chr7:4923615-4923665	GM12892	blood:	n/a
25	chr7:4923615-4923665	HPAEpiC	pulmonary alveolar:	n/a
26	chr7:4923615-4923665	HEEpiC	esophagus:	n/a
27	chr7:4923615-4923665	NB4	blood:	n/a
28	chr7:4923615-4923665	Hela-S3	cervix:	n/a
29	chr7:4923615-4923665	AG04449	skin:	fetal
30	chr7:4923615-4923665	HRPEpiC	eye:	n/a
31	chr7:4923615-4923665	PFSK-1	brain:	n/a
32	chr7:4923615-4923665	HCT-116	colon:	n/a
33	chr7:4923615-4923665	A549	lung:	n/a
34	chr7:4923615-4923665	BJ	skin:	n/a
35	chr7:4923615-4923665	HEK293	kidney:	embryo
36	chr7:4923615-4923665	HRCEpiC	kidney:	n/a
37	chr7:4923615-4923665	HL-60	blood:	n/a
38	chr7:4923615-4923665	U87	brain:	n/a
39	chr7:4923615-4923665	NT2-D1	testis:	n/a
40	chr7:4923615-4923665	GM12878	blood:	n/a
41	chr7:4923615-4923665	Jurkat	blood:	n/a
42	chr7:4923615-4923665	HUVEC	blood vessel:	n/a
43	chr7:4923615-4923665	GM06990	blood:	n/a
44	chr7:4923615-4923665	MCF-7	breast:	n/a
45	chr7:4923615-4923665	HCPEpiC	choroid plexus:	n/a
46	chr7:4923615-4923665	NHDF-neo	bronchial:	n/a
47	chr7:4923615-4923665	HCM	heart:	n/a
48	chr7:4923615-4923665	GM19239	blood:	n/a
49	chr7:4923615-4923665	HepG2	liver:	n/a
50	chr7:4923615-4923665	IMR90	lung:	fetal

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
RADIL	CpG island
ENSG00000196204	Chromatin interaction
ENSG00000272968	Chromatin interaction
ENSG00000146587	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:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4921600-4923800	Active TSS	Aorta	Aorta
2	chr7:4921600-4923800	Active TSS	Brain Angular Gyrus	brain
3	chr7:4921800-4923800	Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chr7:4922200-4923800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr7:4922400-4923800	Active TSS	Breast Myoepithelial Primary Cells	Breast
6	chr7:4922400-4923800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
7	chr7:4922600-4923800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr7:4922600-4923800	Active TSS	Fetal Brain Female	brain
9	chr7:4922600-4923800	Active TSS	HSMM	muscle
10	chr7:4922800-4923800	Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr7:4922800-4923800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr7:4922800-4923800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr7:4922800-4923800	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
14	chr7:4923200-4923800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr7:4923200-4923800	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr7:4923200-4923800	Active TSS	Cortex derived primary cultured neurospheres	brain
17	chr7:4923200-4923800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
18	chr7:4923200-4923800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
19	chr7:4923400-4923800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr7:4923400-4923800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
21	chr7:4923400-4923800	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
22	chr7:4923400-4923800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
23	chr7:4923400-4923800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr7:4923400-4923800	Bivalent/Poised TSS	Colonic Mucosa	Colon
25	chr7:4923400-4923800	Enhancers	Pancreas	Pancrea
26	chr7:4923400-4923800	Enhancers	NHDF-Ad	bronchial
27	chr7:4923400-4928200	Weak transcription	Right Atrium	heart
28	chr7:4923400-4933800	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr7:4923600-4923800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
30	chr7:4923600-4923800	Bivalent/Poised TSS	Primary hematopoietic stem cells short term culture	blood
31	chr7:4923600-4923800	Bivalent/Poised TSS	Primary T helper naive cells fromperipheralblood	blood
32	chr7:4923600-4923800	Enhancers	Fetal Brain Male	brain
33	chr7:4923600-4923800	Bivalent Enhancer	Fetal Stomach	stomach
34	chr7:4923600-4923800	Enhancers	Ovary	ovary

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