Variant report

Variant	rs537936342
Chromosome Location	chr6:31869057-31869058
allele	C/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	chr6:31868140-31869602	HepG2	liver:	n/a	n/a
2	POLR2A	chr6:31868928-31870632	HUVEC	blood vessel:	n/a	n/a
3	POLR2A	chr6:31868974-31870819	HL-60	blood:	n/a	n/a
4	MYC	chr6:31868632-31869208	MCF-7	breast:	n/a	n/a
5	MAX	chr6:31868651-31870305	K562	blood:	n/a	chr6:31869760-31869769 chr6:31869513-31869523 chr6:31869608-31869619 chr6:31869923-31869932 chr6:31869927-31869934
6	E2F6	chr6:31868601-31869154	K562	blood:	n/a	n/a
7	MAX	chr6:31868981-31870445	ECC-1	luminal epithelium:	n/a	chr6:31869760-31869769 chr6:31869513-31869523 chr6:31869608-31869619 chr6:31870306-31870315 chr6:31869923-31869932 chr6:31869927-31869934
8	JUN	chr6:31868159-31870923	K562	blood:	n/a	chr6:31870104-31870113 chr6:31869512-31869521 chr6:31869471-31869480
9	SIN3AK20	chr6:31868928-31870330	K562	blood:	n/a	n/a
10	POLR2A	chr6:31868725-31870941	Hela-S3	cervix:	n/a	n/a
11	POLR2A	chr6:31868709-31870502	Hela-S3	cervix:	n/a	n/a
12	POLR2A	chr6:31868171-31869121	GM12878	blood:	n/a	n/a
13	MYC	chr6:31868864-31869183	K562	blood:	n/a	n/a
14	HCFC1	chr6:31868829-31871106	Hela-S3	cervix:	n/a	n/a
15	POLR2A	chr6:31868468-31870558	MCF-7	breast:	n/a	n/a
16	MYC	chr6:31868712-31870394	K562	blood:	n/a	chr6:31869760-31869769 chr6:31869513-31869523 chr6:31869608-31869619 chr6:31870306-31870315 chr6:31869923-31869932 chr6:31869927-31869934
17	POLR2A	chr6:31868612-31870632	ECC-1	luminal epithelium:	n/a	n/a
18	POLR2A	chr6:31869002-31870395	HEK293	kidney:	n/a	n/a
19	POLR2A	chr6:31868568-31870592	MCF-7	breast:	n/a	n/a
20	MYC	chr6:31868637-31869148	MCF-7	breast:	n/a	n/a
21	POLR2A	chr6:31868766-31869621	SK-N-MC	brain:	n/a	n/a
22	POLR2A	chr6:31868651-31870469	K562	blood:	n/a	n/a
23	POLR2A	chr6:31868883-31871085	HL-60	blood:	n/a	n/a
24	YY1	chr6:31868860-31870378	K562	blood:	n/a	chr6:31870203-31870217 chr6:31869440-31869449 chr6:31870204-31870218 chr6:31869663-31869677 chr6:31870046-31870055 chr6:31869512-31869523 chr6:31869780-31869791 chr6:31869515-31869524 chr6:31869294-31869305 chr6:31869512-31869521 chr6:31869288-31869297 chr6:31869782-31869791 chr6:31869575-31869586
25	EGR1	chr6:31868981-31870403	K562	blood:	n/a	chr6:31869780-31869793 chr6:31870061-31870070 chr6:31869469-31869484 chr6:31869779-31869794 chr6:31870103-31870113 chr6:31869087-31869096 chr6:31869758-31869771 chr6:31869783-31869792 chr6:31869759-31869770 chr6:31869760-31869770 chr6:31869761-31869770 chr6:31869543-31869553 chr6:31870181-31870190 chr6:31869758-31869772 chr6:31869780-31869793 chr6:31869084-31869097 chr6:31869758-31869771 chr6:31869569-31869584 chr6:31869776-31869798 chr6:31869514-31869524 chr6:31869760-31869770 chr6:31869783-31869793 chr6:31869780-31869793 chr6:31869712-31869721 chr6:31869288-31869298 chr6:31869470-31869483 chr6:31870179-31870188 chr6:31869759-31869770 chr6:31870062-31870071
26	ZBTB7A	chr6:31869000-31870150	ECC-1	luminal epithelium:	n/a	chr6:31869679-31869690
27	NR2F2	chr6:31868638-31870149	K562	blood:	n/a	n/a
28	MAX	chr6:31868570-31870590	MCF-7	breast:	n/a	chr6:31869760-31869769 chr6:31869513-31869523 chr6:31869608-31869619 chr6:31870306-31870315 chr6:31869923-31869932 chr6:31869927-31869934
29	POLR2A	chr6:31868579-31870519	MCF-7	breast:	n/a	n/a
30	NR2F2	chr6:31868765-31870596	MCF-7	breast:	n/a	n/a
31	HDAC2	chr6:31868953-31870529	MCF-7	breast:	n/a	chr6:31870180-31870189 chr6:31869760-31869769 chr6:31870182-31870191
32	POLR2A	chr6:31869056-31870464	HCT-116	colon:	n/a	n/a
33	MYC	chr6:31868713-31869066	MCF-7	breast:	n/a	n/a
34	POLR2A	chr6:31868623-31869375	GM12892	blood:	n/a	n/a
35	CREB1	chr6:31869042-31870836	HepG2	liver:	n/a	n/a
36	POLR2A	chr6:31868600-31869502	K562	blood:	n/a	n/a
37	POLR2A	chr6:31868808-31870492	GM12878	blood:	n/a	n/a
38	POLR2A	chr6:31868725-31869088	GM12878	blood:	n/a	n/a
39	POLR2A	chr6:31868575-31869148	HepG2	liver:	n/a	n/a
40	MAX	chr6:31868718-31869674	H1-hESC	embryonic stem cell:	n/a	chr6:31869513-31869523 chr6:31869608-31869619
41	POLR2A	chr6:31868892-31870672	Hela-S3	cervix:	n/a	n/a
42	ELF1	chr6:31868788-31870541	MCF-7	breast:	n/a	chr6:31870205-31870217 chr6:31869672-31869681
43	POLR2A	chr6:31868202-31870803	PFSK-1	brain:	n/a	n/a
44	POLR2A	chr6:31869046-31869074	HUVEC	blood vessel:	n/a	n/a
45	E2F6	chr6:31868622-31869331	H1-hESC	embryonic stem cell:	n/a	chr6:31869288-31869297
46	MAX	chr6:31868886-31870522	MCF-7	breast:	n/a	chr6:31869760-31869769 chr6:31869513-31869523 chr6:31869608-31869619 chr6:31870306-31870315 chr6:31869923-31869932 chr6:31869927-31869934
47	POLR2A	chr6:31868667-31869061	HepG2	liver:	n/a	n/a
48	POLR2A	chr6:31868581-31869098	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr6:31869039-31869619	HCT-116	colon:	n/a	n/a
50	MXI1	chr6:31868748-31870797	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31869057-31869107	RPTEC	kidney:	n/a
2	chr6:31869057-31869107	CMK	blood:	n/a
3	chr6:31869057-31869107	PrEC	prostate:	n/a
4	chr6:31869057-31869107	HRPEpiC	eye:	n/a
5	chr6:31869057-31869107	NHBE	bronchial:	n/a
6	chr6:31869057-31869107	Caco-2	colon:	n/a
7	chr6:31869057-31869107	HL-60	blood:	n/a
8	chr6:31869057-31869107	BJ	skin:	n/a
9	chr6:31869057-31869107	PFSK-1	brain:	n/a
10	chr6:31869057-31869107	HUVEC	blood vessel:	n/a
11	chr6:31869057-31869107	AG04449	skin:	fetal
12	chr6:31869057-31869107	HEEpiC	esophagus:	n/a
13	chr6:31869057-31869107	ovcar-3	ovarian:	n/a
14	chr6:31869057-31869107	GM12878	blood:	n/a
15	chr6:31869057-31869107	LNCaP	prostate:	n/a
16	chr6:31869057-31869107	MCF10A-Er-Src	breast:	n/a
17	chr6:31869057-31869107	NHDF-neo	bronchial:	n/a
18	chr6:31869057-31869107	Hepatocyte	liver:	n/a
19	chr6:31869057-31869107	HRE	kidney:	n/a
20	chr6:31869057-31869107	SKMC	muscle:	n/a
21	chr6:31869057-31869107	HepG2	liver:	n/a
22	chr6:31869057-31869107	HEK293	kidney:	embryo
23	chr6:31869057-31869107	AG09309	skin:	n/a
24	chr6:31869057-31869107	HPAEpiC	pulmonary alveolar:	n/a
25	chr6:31869057-31869107	NH-A	brain:	n/a
26	chr6:31869057-31869107	AG04450	lung:	fetal
27	chr6:31869057-31869107	NB4	blood:	n/a
28	chr6:31869057-31869107	Hela-S3	cervix:	n/a
29	chr6:31869057-31869107	GM19239	blood:	n/a
30	chr6:31869057-31869107	GM12892	blood:	n/a
31	chr6:31869057-31869107	H1-hESC	embryonic stem cell:	embryo
32	chr6:31869057-31869107	SK-N-SH_RA	brain:	n/a
33	chr6:31869057-31869107	A549	lung:	n/a
34	chr6:31869057-31869107	HMEC	breast:	n/a
35	chr6:31869057-31869107	ECC-1	luminal epithelium:	n/a
36	chr6:31869057-31869107	AoSMC	blood vessel:	n/a
37	chr6:31869057-31869107	U87	brain:	n/a
38	chr6:31869057-31869107	HAEpiC	amniotic membrane:	n/a
39	chr6:31869057-31869107	PANC-1	pancreas:	n/a
40	chr6:31869057-31869107	HNPCEpiC	eye:	n/a
41	chr6:31869057-31869107	AG10803	skin:	n/a
42	chr6:31869057-31869107	K562	blood:	n/a
43	chr6:31869057-31869107	HCPEpiC	choroid plexus:	n/a
44	chr6:31869057-31869107	BE2_C	brain:	n/a
45	chr6:31869057-31869107	IMR90	lung:	fetal
46	chr6:31869057-31869107	AG09319	gingival:	n/a
47	chr6:31869057-31869107	HIPEpiC	eye:	n/a
48	chr6:31869057-31869107	ProgFib	skin:	n/a
49	chr6:31869057-31869107	Jurkat	blood:	n/a
50	chr6:31869057-31869107	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:31864040..31872511-chr6:31917614..31930102,27	MCF-7	breast:
2	chr6:31794734..31796775-chr6:31868219..31871084,2	MCF-7	breast:
3	chr6:31761659..31763884-chr6:31868027..31870923,3	K562	blood:
4	chr6:31868623..31870778-chr6:31945874..31948322,2	K562	blood:
5	chr6:31846442..31848048-chr6:31868032..31869941,2	K562	blood:
6	chr6:31782860..31784585-chr6:31867498..31869267,2	K562	blood:
7	chr6:31867895..31873109-chr6:31925613..31930389,7	K562	blood:
8	chr6:31866210..31871385-chr6:31935988..31941288,8	K562	blood:
9	chr6:31509091..31511742-chr6:31868193..31871571,3	MCF-7	breast:
10	chr6:31827799..31831011-chr6:31868395..31870845,5	MCF-7	breast:
11	chr6:31851397..31853749-chr6:31868487..31870497,2	MCF-7	breast:
12	chr6:31801616..31806746-chr6:31865132..31870777,8	MCF-7	breast:
13	chr6:31864133..31871768-chr6:31886295..31891953,13	MCF-7	breast:
14	chr6:31868360..31871056-chr6:32011358..32014091,3	K562	blood:
15	chr6:31867075..31869848-chr6:31926953..31928795,2	K562	blood:
16	chr6:31801352..31804698-chr6:31868339..31871951,3	K562	blood:
17	chr6:31798354..31804916-chr6:31860790..31871982,18	MCF-7	breast:
18	chr6:31868564..31871785-chr6:31887319..31890291,4	MCF-7	breast:
19	chr6:31627970..31635325-chr6:31864036..31871429,12	K562	blood:
20	chr6:31868360..31870239-chr6:32012136..32014091,2	K562	blood:
21	chr6:31828023..31833065-chr6:31863439..31869544,9	K562	blood:
22	chr6:31868502..31871158-chr6:31911705..31915017,4	MCF-7	breast:
23	chr6:31860287..31862319-chr6:31868202..31870669,2	MCF-7	breast:
24	chr6:31631113..31634365-chr6:31867924..31871902,6	K562	blood:
25	chr6:31868614..31871551-chr6:31914927..31918494,4	K562	blood:
26	chr6:31867614..31871926-chr6:31937988..31942087,9	K562	blood:
27	chr6:31868706..31872478-chr6:31938286..31942065,5	MCF-7	breast:
28	chr6:31867879..31871842-chr6:31901664..31905567,4	MCF-7	breast:
29	chr6:31862879..31872535-chr6:31911667..31928766,47	MCF-7	breast:
30	chr6:31868781..31871119-chr6:31892943..31895660,2	MCF-7	breast:
31	chr6:31864068..31872693-chr6:31934470..31941847,12	MCF-7	breast:
32	chr6:31867782..31870627-chr6:32121344..32123906,2	K562	blood:

Variant related genes	Relation type
EHMT2	TF binding region
EHMT2	CpG island
ENSG00000204371	Chromatin interaction
ENSG00000201207	Chromatin interaction
ENSG00000258388	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000168477	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000234006	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000204344	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000204356	Chromatin interaction
ENSG00000237080	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000221988	Chromatin interaction
ENSG00000204314	Chromatin interaction
ENSG00000201754	Chromatin interaction
ENSG00000204439	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000204394	Chromatin interaction
ENSG00000244255	Chromatin interaction
ENSG00000221267	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000204348	Chromatin interaction
ENSG00000243649	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000204351	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:52 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv601610	chr6:31280101-31960770	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	370 gene(s)	inside rSNPs	diseases
2	nsv601628	chr6:31280327-31990098	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
3	nsv601629	chr6:31280327-31996185	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
4	nsv601630	chr6:31280327-32011317	Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer 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	378 gene(s)	inside rSNPs	diseases
5	nsv601631	chr6:31280327-32017540	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
6	nsv1023939	chr6:31325961-32026747	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
7	nsv538188	chr6:31325961-32026747	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
8	nsv1021747	chr6:31386219-31907266	Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	330 gene(s)	inside rSNPs	diseases
9	nsv1033154	chr6:31550614-32009410	Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	326 gene(s)	inside rSNPs	diseases
10	nsv1017945	chr6:31609641-32481240	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
11	esv3428142	chr6:31615800-31881809	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	257 gene(s)	inside rSNPs	diseases
12	nsv884428	chr6:31728102-31870326	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
13	nsv601950	chr6:31785438-32492308	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
14	nsv601951	chr6:31785438-32496748	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
15	nsv601955	chr6:31785453-32484368	Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
16	nsv601956	chr6:31785453-32492308	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
17	nsv884472	chr6:31813898-31870856	Weak transcription Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
18	nsv508399	chr6:31829474-31902423	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
19	nsv884474	chr6:31836055-31870326	Genic enhancers Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
20	nsv462875	chr6:31838441-31907147	Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
21	nsv601960	chr6:31838441-31907147	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
22	nsv884475	chr6:31840625-31880320	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
23	nsv884476	chr6:31848000-31870326	Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
24	nsv884477	chr6:31850724-31870326	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
25	nsv884478	chr6:31850724-31874505	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
26	nsv884479	chr6:31850724-31878433	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
27	nsv884480	chr6:31851234-31870856	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
28	nsv884481	chr6:31851234-31878433	Strong transcription Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
29	nsv884482	chr6:31851234-31880320	Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
30	nsv966619	chr6:31852653-31870444	Flanking Active TSS Strong transcription Active TSS Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	49 gene(s)	inside rSNPs	diseases
31	nsv884484	chr6:31854543-31879158	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	50 gene(s)	inside rSNPs	diseases
32	nsv884485	chr6:31860576-31880320	Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	49 gene(s)	inside rSNPs	diseases
33	nsv884486	chr6:31861207-31869135	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	46 gene(s)	inside rSNPs	diseases
34	nsv884487	chr6:31861207-31870326	Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	48 gene(s)	inside rSNPs	diseases
35	nsv884488	chr6:31861207-31870856	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	48 gene(s)	inside rSNPs	diseases
36	nsv884489	chr6:31861207-31870856	Strong transcription Flanking Active TSS Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	48 gene(s)	inside rSNPs	diseases
37	nsv884490	chr6:31861207-31871485	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	48 gene(s)	inside rSNPs	diseases
38	nsv884491	chr6:31861207-31872551	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	48 gene(s)	inside rSNPs	diseases
39	nsv884492	chr6:31861207-31874505	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	48 gene(s)	inside rSNPs	diseases
40	nsv884493	chr6:31861207-31876647	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	48 gene(s)	inside rSNPs	diseases
41	nsv884494	chr6:31861207-31876647	Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	48 gene(s)	inside rSNPs	diseases
42	nsv884495	chr6:31861207-31878433	Enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	49 gene(s)	inside rSNPs	diseases
43	nsv884496	chr6:31861207-31878495	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	49 gene(s)	inside rSNPs	diseases
44	nsv884497	chr6:31861207-31879158	Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	49 gene(s)	inside rSNPs	diseases
45	nsv884498	chr6:31861207-31880320	Flanking Active TSS Genic enhancers Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	49 gene(s)	inside rSNPs	diseases
46	nsv884499	chr6:31864304-31872551	Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	48 gene(s)	inside rSNPs	diseases
47	nsv884500	chr6:31864304-31873465	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	48 gene(s)	inside rSNPs	diseases
48	nsv884501	chr6:31864304-31874505	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	48 gene(s)	inside rSNPs	diseases
49	nsv884502	chr6:31864304-31876647	Enhancers Active TSS Genic enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	48 gene(s)	inside rSNPs	diseases
50	nsv10822	chr6:31866769-31871690	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	45 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31866600-31869200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
2	chr6:31866800-31869200	Enhancers	Primary T killer memory cells from peripheral blood	blood
3	chr6:31866800-31869200	Weak transcription	Small Intestine	intestine
4	chr6:31866800-31869600	Enhancers	Fetal Heart	heart
5	chr6:31867800-31869200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr6:31868000-31869600	Enhancers	Spleen	Spleen
7	chr6:31868200-31869200	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:31868200-31869400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr6:31868400-31869200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr6:31868400-31869200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr6:31868600-31869200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr6:31868600-31869200	Flanking Active TSS	Brain Cingulate Gyrus	brain
13	chr6:31868600-31869400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr6:31868600-31869400	Flanking Active TSS	Fetal Lung	lung
15	chr6:31868600-31869400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
16	chr6:31868600-31869400	Flanking Active TSS	A549	lung
17	chr6:31868600-31869400	Enhancers	NHDF-Ad	bronchial
18	chr6:31868600-31869600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr6:31868600-31870200	Active TSS	HUES64 Cell Line	embryonic stem cell
20	chr6:31868600-31870400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr6:31868800-31869200	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:31868800-31869200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr6:31868800-31869200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr6:31868800-31869200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr6:31868800-31869200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr6:31868800-31869200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
27	chr6:31868800-31869200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr6:31868800-31869200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr6:31868800-31869200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
30	chr6:31868800-31869200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
31	chr6:31868800-31869200	Enhancers	Aorta	Aorta
32	chr6:31868800-31869200	Flanking Active TSS	Brain Anterior Caudate	brain
33	chr6:31868800-31869200	Flanking Active TSS	Brain Hippocampus Middle	brain
34	chr6:31868800-31869200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
35	chr6:31868800-31869200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
36	chr6:31868800-31869200	Flanking Active TSS	Brain Substantia Nigra	brain
37	chr6:31868800-31869200	Flanking Active TSS	Colon Smooth Muscle	Colon
38	chr6:31868800-31869200	Flanking Active TSS	Duodenum Mucosa	Duodenum
39	chr6:31868800-31869200	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
40	chr6:31868800-31869200	Flanking Active TSS	Fetal Stomach	stomach
41	chr6:31868800-31869200	Flanking Active TSS	Pancreas	Pancrea
42	chr6:31868800-31869200	Flanking Active TSS	Placenta Amnion	Placenta Amnion
43	chr6:31868800-31869200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
44	chr6:31868800-31869200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
45	chr6:31868800-31869200	Flanking Active TSS	HepG2	liver
46	chr6:31868800-31869200	Flanking Active TSS	K562	blood
47	chr6:31868800-31869200	Flanking Active TSS	NHEK	skin
48	chr6:31868800-31869200	Flanking Active TSS	NHLF	lung
49	chr6:31868800-31869400	Active TSS	ES-I3 Cell Line	embryonic stem cell
50	chr6:31868800-31869400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell

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