Variant report

Variant	rs376539476
Chromosome Location	chr6:31868828-31868829
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:81)
CpG islands
(count:244)
Chromatin interactive
region (count:34)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:81 , 50 per page) page: 1 2

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	chr6:31868622-31868944	HCT-116	colon:	n/a	n/a
3	MYC	chr6:31868692-31868839	HepG2	liver:	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	CTCF	chr6:31868640-31868881	MCF-7	breast:	n/a	n/a
8	JUN	chr6:31868159-31870923	K562	blood:	n/a	chr6:31870104-31870113 chr6:31869512-31869521 chr6:31869471-31869480
9	POLR2A	chr6:31868629-31868930	HCT-116	colon:	n/a	n/a
10	CTCF	chr6:31868730-31868829	MCF-7	breast:	n/a	n/a
11	POLR2A	chr6:31868641-31869039	H1-hESC	embryonic stem cell:	n/a	n/a
12	POLR2A	chr6:31868725-31870941	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr6:31868709-31870502	Hela-S3	cervix:	n/a	n/a
14	MYC	chr6:31868736-31869027	MCF-7	breast:	n/a	n/a
15	POLR2A	chr6:31868171-31869121	GM12878	blood:	n/a	n/a
16	POLR2A	chr6:31868468-31870558	MCF-7	breast:	n/a	n/a
17	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
18	CTCF	chr6:31868700-31868850	GM12871	blood:	n/a	n/a
19	POLR2A	chr6:31868612-31870632	ECC-1	luminal epithelium:	n/a	n/a
20	PML	chr6:31868586-31869027	K562	blood:	n/a	n/a
21	POLR2A	chr6:31868568-31870592	MCF-7	breast:	n/a	n/a
22	MYC	chr6:31868637-31869148	MCF-7	breast:	n/a	n/a
23	POLR2A	chr6:31868766-31869621	SK-N-MC	brain:	n/a	n/a
24	POLR2A	chr6:31868651-31870469	K562	blood:	n/a	n/a
25	NR2F2	chr6:31868638-31870149	K562	blood:	n/a	n/a
26	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
27	POLR2A	chr6:31868579-31870519	MCF-7	breast:	n/a	n/a
28	NR2F2	chr6:31868765-31870596	MCF-7	breast:	n/a	n/a
29	MYC	chr6:31868713-31869066	MCF-7	breast:	n/a	n/a
30	POLR2A	chr6:31868623-31869375	GM12892	blood:	n/a	n/a
31	TEAD4	chr6:31868617-31868984	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr6:31868707-31868989	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr6:31868600-31869502	K562	blood:	n/a	n/a
34	POLR2A	chr6:31868808-31870492	GM12878	blood:	n/a	n/a
35	POLR2A	chr6:31868725-31869088	GM12878	blood:	n/a	n/a
36	POLR2A	chr6:31868575-31869148	HepG2	liver:	n/a	n/a
37	MAX	chr6:31868718-31869674	H1-hESC	embryonic stem cell:	n/a	chr6:31869513-31869523 chr6:31869608-31869619
38	POLR2A	chr6:31868774-31868830	GM12878	blood:	n/a	n/a
39	ELF1	chr6:31868788-31870541	MCF-7	breast:	n/a	chr6:31870205-31870217 chr6:31869672-31869681
40	POLR2A	chr6:31868202-31870803	PFSK-1	brain:	n/a	n/a
41	TEAD4	chr6:31868629-31869011	H1-hESC	embryonic stem cell:	n/a	n/a
42	E2F6	chr6:31868622-31869331	H1-hESC	embryonic stem cell:	n/a	chr6:31869288-31869297
43	MAX	chr6:31868623-31868840	H1-hESC	embryonic stem cell:	n/a	n/a
44	HEY1	chr6:31868703-31869002	K562	blood:	n/a	n/a
45	POLR2A	chr6:31868667-31869061	HepG2	liver:	n/a	n/a
46	POLR2A	chr6:31868581-31869098	H1-hESC	embryonic stem cell:	n/a	n/a
47	MXI1	chr6:31868748-31870797	IMR90	lung:	n/a	n/a
48	TEAD4	chr6:31868510-31869526	K562	blood:	n/a	n/a
49	MAX	chr6:31868751-31870555	ECC-1	luminal epithelium:	n/a	chr6:31869760-31869769 chr6:31869513-31869523 chr6:31869608-31869619 chr6:31870306-31870315 chr6:31869923-31869932 chr6:31869927-31869934
50	E2F6	chr6:31868628-31869247	H1-hESC	embryonic stem cell:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31868797-31868847	MCF-7	breast:	n/a
2	chr6:31868809-31868859	SK-N-SH	brain:	n/a
3	chr6:31868797-31868847	A549	lung:	n/a
4	chr6:31868797-31868847	BJ	skin:	n/a
5	chr6:31868782-31868832	HNPCEpiC	eye:	n/a
6	chr6:31868813-31868863	T-47D	breast:	n/a
7	chr6:31868813-31868863	U87	brain:	n/a
8	chr6:31868809-31868859	MCF10A-Er-Src	breast:	n/a
9	chr6:31868797-31868847	Hepatocyte	liver:	n/a
10	chr6:31868797-31868847	CMK	blood:	n/a
11	chr6:31868782-31868832	GM12878	blood:	n/a
12	chr6:31868813-31868863	HRCEpiC	kidney:	n/a
13	chr6:31868797-31868847	HCM	heart:	n/a
14	chr6:31868782-31868832	IMR90	lung:	fetal
15	chr6:31868809-31868859	BE2_C	brain:	n/a
16	chr6:31868809-31868859	HRE	kidney:	n/a
17	chr6:31868782-31868832	NH-A	brain:	n/a
18	chr6:31868813-31868863	NH-A	brain:	n/a
19	chr6:31868813-31868863	HRE	kidney:	n/a
20	chr6:31868797-31868847	ECC-1	luminal epithelium:	n/a
21	chr6:31868809-31868859	ovcar-3	ovarian:	n/a
22	chr6:31868782-31868832	HIPEpiC	eye:	n/a
23	chr6:31868797-31868847	SK-N-SH_RA	brain:	n/a
24	chr6:31868782-31868832	GM06990	blood:	n/a
25	chr6:31868797-31868847	HUVEC	blood vessel:	n/a
26	chr6:31868782-31868832	ovcar-3	ovarian:	n/a
27	chr6:31868813-31868863	AG04450	lung:	fetal
28	chr6:31868797-31868847	GM19239	blood:	n/a
29	chr6:31868782-31868832	PrEC	prostate:	n/a
30	chr6:31868797-31868847	GM12878	blood:	n/a
31	chr6:31868797-31868847	HAEpiC	amniotic membrane:	n/a
32	chr6:31868782-31868832	HEEpiC	esophagus:	n/a
33	chr6:31868797-31868847	HCT-116	colon:	n/a
34	chr6:31868813-31868863	Hepatocyte	liver:	n/a
35	chr6:31868797-31868847	NT2-D1	testis:	n/a
36	chr6:31868809-31868859	HNPCEpiC	eye:	n/a
37	chr6:31868782-31868832	BJ	skin:	n/a
38	chr6:31868809-31868859	SK-N-SH_RA	brain:	n/a
39	chr6:31868813-31868863	ovcar-3	ovarian:	n/a
40	chr6:31868782-31868832	MCF10A-Er-Src	breast:	n/a
41	chr6:31868809-31868859	HCF	heart:	n/a
42	chr6:31868782-31868832	PANC-1	pancreas:	n/a
43	chr6:31868809-31868859	HPAEpiC	pulmonary alveolar:	n/a
44	chr6:31868797-31868847	HCF	heart:	n/a
45	chr6:31868813-31868863	SK-N-SH_RA	brain:	n/a
46	chr6:31868813-31868863	HPAEpiC	pulmonary alveolar:	n/a
47	chr6:31868809-31868859	Hepatocyte	liver:	n/a
48	chr6:31868782-31868832	RPTEC	kidney:	n/a
49	chr6:31868797-31868847	GM12891	blood:	n/a
50	chr6:31868809-31868859	AG04449	skin:	fetal

(count:34 , 50 per page) page: 1

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	chr6:31844613..31847430-chr6:31865372..31868871,3	MCF-7	breast:
7	chr6:31782860..31784585-chr6:31867498..31869267,2	K562	blood:
8	chr6:31793170..31796834-chr6:31863715..31868848,6	K562	blood:
9	chr6:31867895..31873109-chr6:31925613..31930389,7	K562	blood:
10	chr6:31866210..31871385-chr6:31935988..31941288,8	K562	blood:
11	chr6:31509091..31511742-chr6:31868193..31871571,3	MCF-7	breast:
12	chr6:31827799..31831011-chr6:31868395..31870845,5	MCF-7	breast:
13	chr6:31851397..31853749-chr6:31868487..31870497,2	MCF-7	breast:
14	chr6:31801616..31806746-chr6:31865132..31870777,8	MCF-7	breast:
15	chr6:31864133..31871768-chr6:31886295..31891953,13	MCF-7	breast:
16	chr6:31868360..31871056-chr6:32011358..32014091,3	K562	blood:
17	chr6:31867075..31869848-chr6:31926953..31928795,2	K562	blood:
18	chr6:31801352..31804698-chr6:31868339..31871951,3	K562	blood:
19	chr6:31798354..31804916-chr6:31860790..31871982,18	MCF-7	breast:
20	chr6:31868564..31871785-chr6:31887319..31890291,4	MCF-7	breast:
21	chr6:31627970..31635325-chr6:31864036..31871429,12	K562	blood:
22	chr6:31868360..31870239-chr6:32012136..32014091,2	K562	blood:
23	chr6:31828023..31833065-chr6:31863439..31869544,9	K562	blood:
24	chr6:31868502..31871158-chr6:31911705..31915017,4	MCF-7	breast:
25	chr6:31860287..31862319-chr6:31868202..31870669,2	MCF-7	breast:
26	chr6:31631113..31634365-chr6:31867924..31871902,6	K562	blood:
27	chr6:31868614..31871551-chr6:31914927..31918494,4	K562	blood:
28	chr6:31867614..31871926-chr6:31937988..31942087,9	K562	blood:
29	chr6:31868706..31872478-chr6:31938286..31942065,5	MCF-7	breast:
30	chr6:31867879..31871842-chr6:31901664..31905567,4	MCF-7	breast:
31	chr6:31862879..31872535-chr6:31911667..31928766,47	MCF-7	breast:
32	chr6:31868781..31871119-chr6:31892943..31895660,2	MCF-7	breast:
33	chr6:31864068..31872693-chr6:31934470..31941847,12	MCF-7	breast:
34	chr6:31867782..31870627-chr6:32121344..32123906,2	K562	blood:

No data

Variant related genes	Relation type
EHMT2	TF binding region
EHMT2	CpG island
ENSG00000234006	Chromatin interaction
ENSG00000204314	Chromatin interaction
ENSG00000201754	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000168477	Chromatin interaction
ENSG00000244255	Chromatin interaction
ENSG00000204351	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000221267	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000258388	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000204356	Chromatin interaction
ENSG00000243649	Chromatin interaction
ENSG00000204344	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000201207	Chromatin interaction
ENSG00000237080	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000204394	Chromatin interaction
ENSG00000221988	Chromatin interaction
ENSG00000204348	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000204439	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000204385	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	chr6:31866400-31869000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:31866600-31869200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr6:31866800-31869000	Enhancers	Primary T cells fromperipheralblood	blood
4	chr6:31866800-31869000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr6:31866800-31869000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr6:31866800-31869000	Enhancers	Left Ventricle	heart
7	chr6:31866800-31869000	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr6:31866800-31869200	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr6:31866800-31869200	Weak transcription	Small Intestine	intestine
10	chr6:31866800-31869600	Enhancers	Fetal Heart	heart
11	chr6:31867200-31869000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr6:31867200-31869000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr6:31867200-31869000	Weak transcription	Psoas Muscle	Psoas
14	chr6:31867400-31869000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr6:31867600-31869000	Enhancers	Gastric	stomach
16	chr6:31867800-31869000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr6:31867800-31869200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr6:31868000-31869000	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr6:31868000-31869000	Weak transcription	Thymus	Thymus
20	chr6:31868000-31869600	Enhancers	Spleen	Spleen
21	chr6:31868200-31869000	Enhancers	Primary T cells from cord blood	blood
22	chr6:31868200-31869000	Transcr. at gene 5' and 3'	Brain Germinal Matrix	brain
23	chr6:31868200-31869200	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr6:31868200-31869400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr6:31868400-31869000	Flanking Active TSS	Fetal Brain Female	brain
26	chr6:31868400-31869000	Enhancers	Placenta	Placenta
27	chr6:31868400-31869200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr6:31868400-31869200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr6:31868600-31869000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr6:31868600-31869000	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr6:31868600-31869000	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr6:31868600-31869000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr6:31868600-31869000	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr6:31868600-31869000	Weak transcription	Primary B cells from peripheral blood	blood
35	chr6:31868600-31869000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr6:31868600-31869000	Enhancers	Primary T helper cells PMA-I stimulated	--
37	chr6:31868600-31869000	Enhancers	Right Ventricle	heart
38	chr6:31868600-31869200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr6:31868600-31869200	Flanking Active TSS	Brain Cingulate Gyrus	brain
40	chr6:31868600-31869400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr6:31868600-31869400	Flanking Active TSS	Fetal Lung	lung
42	chr6:31868600-31869400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
43	chr6:31868600-31869400	Flanking Active TSS	A549	lung
44	chr6:31868600-31869400	Enhancers	NHDF-Ad	bronchial
45	chr6:31868600-31869600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr6:31868600-31870200	Active TSS	HUES64 Cell Line	embryonic stem cell
47	chr6:31868600-31870400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr6:31868800-31869000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr6:31868800-31869000	Transcr. at gene 5' and 3'	H1 Cell Line	embryonic stem cell
50	chr6:31868800-31869000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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