Variant report

Variant	rs375794318
Chromosome Location	chr6:31869352-31869353
allele	A/G
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	PML	chr6:31869334-31870431	MCF-7	breast:	n/a	n/a
3	MAZ	chr6:31869261-31870511	Hela-S3	cervix:	n/a	chr6:31869760-31869769 chr6:31869513-31869523 chr6:31869608-31869619 chr6:31870306-31870315 chr6:31869923-31869932 chr6:31869927-31869934
4	STAT5A	chr6:31869086-31870196	GM12878	blood:	n/a	chr6:31869776-31869788 chr6:31869436-31869448 chr6:31869893-31869905 chr6:31869469-31869481 chr6:31869656-31869668
5	BHLHE40	chr6:31869276-31870379	K562	blood:	n/a	chr6:31870210-31870226 chr6:31869776-31869792 chr6:31870202-31870218
6	RCOR1	chr6:31869282-31870644	IMR90	lung:	n/a	n/a
7	POLR2A	chr6:31868928-31870632	HUVEC	blood vessel:	n/a	n/a
8	POLR2A	chr6:31868974-31870819	HL-60	blood:	n/a	n/a
9	MAX	chr6:31868651-31870305	K562	blood:	n/a	chr6:31869760-31869769 chr6:31869513-31869523 chr6:31869608-31869619 chr6:31869923-31869932 chr6:31869927-31869934
10	JUND	chr6:31869189-31869684	A549	lung:	n/a	chr6:31869512-31869521 chr6:31869471-31869480
11	POLR2A	chr6:31869341-31870397	GM15510	blood:	n/a	n/a
12	BACH1	chr6:31869336-31870597	H1-hESC	embryonic stem cell:	n/a	n/a
13	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
14	JUN	chr6:31868159-31870923	K562	blood:	n/a	chr6:31870104-31870113 chr6:31869512-31869521 chr6:31869471-31869480
15	SIN3AK20	chr6:31868928-31870330	K562	blood:	n/a	n/a
16	CEBPD	chr6:31869135-31870391	K562	blood:	n/a	n/a
17	PML	chr6:31869111-31870304	MCF-7	breast:	n/a	n/a
18	POLR2A	chr6:31868725-31870941	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr6:31868709-31870502	Hela-S3	cervix:	n/a	n/a
20	POLR2A	chr6:31869224-31870368	HUVEC	blood vessel:	n/a	n/a
21	POLR2A	chr6:31869346-31870530	H1-neurons	neurons:	n/a	n/a
22	POLR2A	chr6:31869144-31870403	A549	lung:	n/a	n/a
23	HCFC1	chr6:31868829-31871106	Hela-S3	cervix:	n/a	n/a
24	EGR1	chr6:31869140-31870259	K562	blood:	n/a	chr6:31869780-31869793 chr6:31870061-31870070 chr6:31869469-31869484 chr6:31869779-31869794 chr6:31870103-31870113 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 chr6:31869758-31869771 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
25	POLR2A	chr6:31868468-31870558	MCF-7	breast:	n/a	n/a
26	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
27	CREB1	chr6:31869287-31869660	A549	lung:	n/a	n/a
28	MYC	chr6:31869231-31870367	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	chr6:31868612-31870632	ECC-1	luminal epithelium:	n/a	n/a
30	POLR2A	chr6:31869002-31870395	HEK293	kidney:	n/a	n/a
31	POLR2A	chr6:31868568-31870592	MCF-7	breast:	n/a	n/a
32	POLR2A	chr6:31868766-31869621	SK-N-MC	brain:	n/a	n/a
33	POLR2A	chr6:31868651-31870469	K562	blood:	n/a	n/a
34	POLR2A	chr6:31869159-31869447	SK-N-SH	brain:	n/a	n/a
35	SIN3AK20	chr6:31869100-31870447	PANC-1	pancreas:	n/a	n/a
36	POLR2A	chr6:31868883-31871085	HL-60	blood:	n/a	n/a
37	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
38	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
39	ZBTB7A	chr6:31869000-31870150	ECC-1	luminal epithelium:	n/a	chr6:31869679-31869690
40	NR2F2	chr6:31868638-31870149	K562	blood:	n/a	n/a
41	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
42	POLR2A	chr6:31868579-31870519	MCF-7	breast:	n/a	n/a
43	NR2F2	chr6:31868765-31870596	MCF-7	breast:	n/a	n/a
44	POLR2A	chr6:31869121-31870509	ECC-1	luminal epithelium:	n/a	n/a
45	BCL3	chr6:31869271-31870396	GM12878	blood:	n/a	chr6:31869712-31869725 chr6:31869468-31869477 chr6:31869780-31869789 chr6:31870205-31870218 chr6:31869292-31869305 chr6:31870203-31870216 chr6:31869312-31869325 chr6:31869514-31869523
46	TAF1	chr6:31869157-31870497	ECC-1	luminal epithelium:	n/a	n/a
47	HDAC2	chr6:31868953-31870529	MCF-7	breast:	n/a	chr6:31870180-31870189 chr6:31869760-31869769 chr6:31870182-31870191
48	POLR2A	chr6:31869056-31870464	HCT-116	colon:	n/a	n/a
49	SMARCB1	chr6:31869310-31870393	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr6:31869249-31869408	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31869304-31869354	HMEC	breast:	n/a
2	chr6:31869304-31869354	HCT-116	colon:	n/a
3	chr6:31869304-31869354	HCF	heart:	n/a
4	chr6:31869304-31869354	IMR90	lung:	fetal
5	chr6:31869304-31869354	Hepatocyte	liver:	n/a
6	chr6:31869304-31869354	A549	lung:	n/a
7	chr6:31869304-31869354	HAEpiC	amniotic membrane:	n/a
8	chr6:31869304-31869354	NHBE	bronchial:	n/a
9	chr6:31869304-31869354	AG10803	skin:	n/a
10	chr6:31869304-31869354	HNPCEpiC	eye:	n/a
11	chr6:31869304-31869354	Hela-S3	cervix:	n/a
12	chr6:31869304-31869354	ovcar-3	ovarian:	n/a
13	chr6:31869304-31869354	HCPEpiC	choroid plexus:	n/a
14	chr6:31869304-31869354	ECC-1	luminal epithelium:	n/a
15	chr6:31869304-31869354	ProgFib	skin:	n/a
16	chr6:31869304-31869354	SK-N-SH	brain:	n/a
17	chr6:31869304-31869354	HPAEpiC	pulmonary alveolar:	n/a
18	chr6:31869304-31869354	HUVEC	blood vessel:	n/a
19	chr6:31869304-31869354	AoSMC	blood vessel:	n/a
20	chr6:31869304-31869354	GM19239	blood:	n/a
21	chr6:31869304-31869354	HepG2	liver:	n/a
22	chr6:31869304-31869354	SK-N-MC	brain:	n/a
23	chr6:31869304-31869354	SK-N-SH_RA	brain:	n/a
24	chr6:31869304-31869354	HRCEpiC	kidney:	n/a
25	chr6:31869304-31869354	HL-60	blood:	n/a
26	chr6:31869304-31869354	Caco-2	colon:	n/a
27	chr6:31869304-31869354	RPTEC	kidney:	n/a
28	chr6:31869304-31869354	MCF-7	breast:	n/a
29	chr6:31869304-31869354	BE2_C	brain:	n/a
30	chr6:31869304-31869354	CMK	blood:	n/a
31	chr6:31869304-31869354	SKMC	muscle:	n/a
32	chr6:31869304-31869354	GM12892	blood:	n/a
33	chr6:31869304-31869354	MCF10A-Er-Src	breast:	n/a
34	chr6:31869304-31869354	HIPEpiC	eye:	n/a
35	chr6:31869304-31869354	NH-A	brain:	n/a
36	chr6:31869304-31869354	AG04450	lung:	fetal
37	chr6:31869304-31869354	HRPEpiC	eye:	n/a
38	chr6:31869304-31869354	PANC-1	pancreas:	n/a
39	chr6:31869304-31869354	K562	blood:	n/a
40	chr6:31869304-31869354	NHDF-neo	bronchial:	n/a
41	chr6:31869304-31869354	PFSK-1	brain:	n/a
42	chr6:31869304-31869354	NB4	blood:	n/a
43	chr6:31869304-31869354	HCM	heart:	n/a
44	chr6:31869304-31869354	H1-hESC	embryonic stem cell:	embryo
45	chr6:31869304-31869354	PrEC	prostate:	n/a
46	chr6:31869304-31869354	HRE	kidney:	n/a
47	chr6:31869304-31869354	Jurkat	blood:	n/a
48	chr6:31869304-31869354	AG09309	skin:	n/a
49	chr6:31869304-31869354	HEK293	kidney:	embryo
50	chr6:31869304-31869354	AG04449	skin:	fetal

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	chr6:31869231..31871840-chr6:31901304..31905157,3	MCF-7	breast:
6	chr6:31846442..31848048-chr6:31868032..31869941,2	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	chr17:61904476..61906775-chr6:31869076..31871321,2	MCF-7	breast:
19	chr6:31868564..31871785-chr6:31887319..31890291,4	MCF-7	breast:
20	chr6:31627970..31635325-chr6:31864036..31871429,12	K562	blood:
21	chr6:31868360..31870239-chr6:32012136..32014091,2	K562	blood:
22	chr6:31828023..31833065-chr6:31863439..31869544,9	K562	blood:
23	chr6:31795326..31798240-chr6:31869248..31870828,2	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	chr6:31869193..31873526-chr6:31908186..31911581,4	MCF-7	breast:
28	chr6:31868614..31871551-chr6:31914927..31918494,4	K562	blood:
29	chr6:31867614..31871926-chr6:31937988..31942087,9	K562	blood:
30	chr6:31868706..31872478-chr6:31938286..31942065,5	MCF-7	breast:
31	chr6:31867879..31871842-chr6:31901664..31905567,4	MCF-7	breast:
32	chr6:31862879..31872535-chr6:31911667..31928766,47	MCF-7	breast:
33	chr6:31868781..31871119-chr6:31892943..31895660,2	MCF-7	breast:
34	chr6:31864068..31872693-chr6:31934470..31941847,12	MCF-7	breast:
35	chr6:31867782..31870627-chr6:32121344..32123906,2	K562	blood:

Variant related genes	Relation type
EHMT2	TF binding region
EHMT2	CpG island
ENSG00000204356	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000234006	Chromatin interaction
ENSG00000204348	Chromatin interaction
ENSG00000204394	Chromatin interaction
ENSG00000204314	Chromatin interaction
ENSG00000108592	Chromatin interaction
ENSG00000204351	Chromatin interaction
ENSG00000087191	Chromatin interaction
ENSG00000168477	Chromatin interaction
ENSG00000201207	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000237080	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000221267	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000243649	Chromatin interaction
ENSG00000204439	Chromatin interaction
ENSG00000258388	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000204344	Chromatin interaction
ENSG00000244255	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000201754	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000221988	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:51 , 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	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
34	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
35	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
36	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
37	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
38	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
39	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
40	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
41	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
42	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
43	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
44	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
45	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
46	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
47	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
48	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
49	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
50	nsv601961	chr6:31868322-32484368	Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 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	chr6:31866800-31869600	Enhancers	Fetal Heart	heart
2	chr6:31868000-31869600	Enhancers	Spleen	Spleen
3	chr6:31868200-31869400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr6:31868600-31869400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:31868600-31869400	Flanking Active TSS	Fetal Lung	lung
6	chr6:31868600-31869400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
7	chr6:31868600-31869400	Flanking Active TSS	A549	lung
8	chr6:31868600-31869400	Enhancers	NHDF-Ad	bronchial
9	chr6:31868600-31869600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr6:31868600-31870200	Active TSS	HUES64 Cell Line	embryonic stem cell
11	chr6:31868600-31870400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr6:31868800-31869400	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr6:31868800-31869400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
14	chr6:31868800-31869400	Flanking Active TSS	Primary B cells from cord blood	blood
15	chr6:31868800-31869400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
16	chr6:31868800-31869400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
17	chr6:31868800-31869400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr6:31868800-31869400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
19	chr6:31868800-31869400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr6:31868800-31869400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr6:31868800-31869400	Flanking Active TSS	Adipose Nuclei	Adipose
22	chr6:31868800-31869400	Flanking Active TSS	Liver	Liver
23	chr6:31868800-31869400	Flanking Active TSS	Colonic Mucosa	Colon
24	chr6:31868800-31869400	Flanking Active TSS	Fetal Intestine Large	intestine
25	chr6:31868800-31869400	Flanking Active TSS	Fetal Muscle Trunk	muscle
26	chr6:31868800-31869400	Flanking Active TSS	Fetal Muscle Leg	muscle
27	chr6:31868800-31869400	Enhancers	Sigmoid Colon	Sigmoid Colon
28	chr6:31868800-31869400	Enhancers	Stomach Mucosa	stomach
29	chr6:31868800-31869400	Flanking Active TSS	Stomach Smooth Muscle	stomach
30	chr6:31868800-31869400	Flanking Active TSS	GM12878-XiMat	blood
31	chr6:31868800-31869400	Flanking Active TSS	HMEC	breast
32	chr6:31868800-31869400	Flanking Active TSS	HUVEC	blood vessel
33	chr6:31868800-31869400	Flanking Active TSS	NH-A	brain
34	chr6:31868800-31869600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr6:31868800-31869600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
36	chr6:31868800-31869800	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr6:31868800-31870400	Active TSS	H9 Cell Line	embryonic stem cell
38	chr6:31868800-31870400	Active TSS	iPS-15b Cell Line	embryonic stem cell
39	chr6:31868800-31870400	Active TSS	Fetal Kidney	kidney
40	chr6:31868800-31870400	Active TSS	Rectal Mucosa Donor 29	rectum
41	chr6:31868800-31870400	Active TSS	Hela-S3	cervix
42	chr6:31868800-31870400	Active TSS	HSMMtube	muscle
43	chr6:31868800-31870400	Active TSS	Osteobl	bone
44	chr6:31868800-31870600	Active TSS	Rectal Smooth Muscle	rectum
45	chr6:31868800-31870800	Active TSS	HSMM	muscle
46	chr6:31869000-31869400	Flanking Active TSS	H1 Cell Line	embryonic stem cell
47	chr6:31869000-31869400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr6:31869000-31869400	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr6:31869000-31869400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
50	chr6:31869000-31869400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood

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