Variant report

Variant	rs2904787
Chromosome Location	chr6:31459768-31459769
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	CTCF	chr6:31459740-31459890	HepG2	liver:	n/a	chr6:31459876-31459883 chr6:31459872-31459890
2	BCLAF1	chr6:31459573-31460031	GM12878	blood:	n/a	n/a
3	SMC3	chr6:31459707-31460066	Hela-S3	cervix:	n/a	chr6:31459874-31459888
4	CTCF	chr6:31459744-31460015	ProgFib	skin:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
5	CTCF	chr6:31459751-31459963	SK-N-SH_RA	brain:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
6	PAX5	chr6:31459542-31459970	GM12878	blood:	n/a	n/a
7	RAD21	chr6:31459699-31460028	HepG2	liver:	n/a	chr6:31459873-31459892 chr6:31459874-31459883
8	CTCF	chr6:31459734-31460014	Lung_OC	lung:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
9	CTCF	chr6:31459751-31460012	NHEK	skin:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
10	BRCA1	chr6:31459755-31459971	Hela-S3	cervix:	n/a	n/a
11	SP1	chr6:31459686-31459945	GM12878	blood:	n/a	n/a
12	CTCF	chr6:31459760-31459910	WI-38	lung:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
13	ZNF143	chr6:31459751-31459988	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr6:31459740-31459890	GM12865	blood:	n/a	chr6:31459876-31459883 chr6:31459872-31459890
15	CTCF	chr6:31459666-31460039	H1-hESC	embryonic stem cell:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
16	CTCF	chr6:31459731-31459999	LNCaP	prostate:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
17	RUNX3	chr6:31459604-31460049	GM12878	blood:	n/a	n/a
18	CTCF	chr6:31459762-31459985	GM20000	blood:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
19	CTCF	chr6:31459491-31460141	SK-N-SH	brain:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
20	CTCF	chr6:31459655-31460102	K562	blood:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
21	MYC	chr6:31459760-31459960	MCF10A-Er-Src	breast:	n/a	n/a
22	CTCF	chr6:31459740-31459890	HCFaa	heart:	n/a	chr6:31459876-31459883 chr6:31459872-31459890
23	MYBL2	chr6:31459648-31460116	HepG2	liver:	n/a	n/a
24	CTCF	chr6:31459703-31459955	HepG2	liver:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
25	CTCF	chr6:31459739-31460009	Fibrobl	skin:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
26	CTCF	chr6:31459752-31460017	GM12892	blood:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
27	CTCF	chr6:31459660-31460114	MCF-7	breast:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
28	CTCF	chr6:31459753-31459996	Medullo	brain:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
29	BHLHE40	chr6:31459742-31459942	K562	blood:	n/a	n/a
30	CTCF	chr6:31459657-31460124	A549	lung:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
31	FOS	chr6:31459739-31459919	MCF10A-Er-Src	breast:	n/a	n/a
32	CTCF	chr6:31459744-31460022	LNCaP	prostate:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
33	RAD21	chr6:31459715-31460052	Hela-S3	cervix:	n/a	chr6:31459873-31459892 chr6:31459874-31459883
34	MAX	chr6:31459730-31459986	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr6:31459740-31459890	GM12875	blood:	n/a	chr6:31459876-31459883 chr6:31459872-31459890
36	RAD21	chr6:31459750-31459993	H1-hESC	embryonic stem cell:	n/a	chr6:31459873-31459892 chr6:31459874-31459883
37	CTCF	chr6:31459721-31460019	K562	blood:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
38	RCOR1	chr6:31459688-31459882	GM12878	blood:	n/a	n/a
39	ZNF143	chr6:31459765-31459955	Hela-S3	cervix:	n/a	n/a
40	EP300	chr6:31459738-31459964	K562	blood:	n/a	n/a
41	CTCF	chr6:31459750-31460005	HepG2	liver:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
42	STAT3	chr6:31459680-31459972	MCF10A-Er-Src	breast:	n/a	n/a
43	CEBPB	chr6:31459658-31459957	Hela-S3	cervix:	n/a	n/a
44	CUX1	chr6:31459767-31460065	K562	blood:	n/a	n/a
45	POLR2A	chr6:31459723-31460044	HCT-116	colon:	n/a	n/a
46	CTCF	chr6:31459746-31460008	GM10266	blood:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
47	CTCF	chr6:31459742-31460017	GM19240	blood:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
48	CTCF	chr6:31459586-31460021	HepG2	liver:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895
49	RCOR1	chr6:31459684-31460065	K562	blood:	n/a	n/a
50	CTCF	chr6:31459745-31460021	A549	lung:	n/a	chr6:31459876-31459883 chr6:31459872-31459890 chr6:31459874-31459895

No.	Distal block	Cell Line	Cell type
1	chr6:31459629..31460383-chr6:31566089..31567042,2	MCF-7	breast:
2	chr6:31458267..31460051-chr6:31509847..31511865,2	K562	blood:
3	chr6:31459710..31467567-chr6:31506191..31511027,18	MCF-7	breast:
4	chr6:31459680..31461470-chr6:31496215..31498262,2	MCF-7	breast:
5	chr6:31458751..31460281-chr6:31589916..31591938,2	K562	blood:
6	chr6:31458384..31468965-chr6:31503613..31512721,28	K562	blood:
7	chr6:31367471..31370049-chr6:31458243..31460002,3	K562	blood:
8	chr6:31456114..31459905-chr6:31495934..31499103,3	K562	blood:

Variant related genes	Relation type
MICB	TF binding region
ENSG00000234006	Chromatin interaction
ENSG00000206337	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000204511	Chromatin interaction
ENSG00000201785	Chromatin interaction
ENSG00000265236	Chromatin interaction
ENSG00000200816	Chromatin interaction
ENSG00000199332	Chromatin interaction

Extended variants
information (count: 87 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs2395033	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2395038	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2395041	0.83[ASN][1000 genomes]
rs2395042	0.84[ASN][1000 genomes]
rs2395043	0.83[ASN][1000 genomes]
rs2395044	0.80[ASN][1000 genomes]
rs2507971	0.85[ASN][1000 genomes]
rs2894222	0.80[ASN][1000 genomes]
rs2904783	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2904786	0.91[AFR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2905729	0.89[AFR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2905738	0.81[EUR][1000 genomes]
rs3130921	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs3130922	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9267247	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:72 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015372	chr6:30704734-31582152	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
2	nsv538173	chr6:30704734-31582152	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
3	nsv428140	chr6:31028290-31462106	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	89 gene(s)	inside rSNPs	diseases
4	esv2758042	chr6:31028290-31497106	Weak transcription Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	101 gene(s)	inside rSNPs	diseases
5	esv2759414	chr6:31028290-31542308	Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	151 gene(s)	inside rSNPs	diseases
6	esv3381377	chr6:31192213-31498578	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	72 gene(s)	inside rSNPs	diseases
7	esv3340592	chr6:31192248-31498535	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	72 gene(s)	inside rSNPs	diseases
8	nsv1021052	chr6:31206639-31485736	Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
9	nsv1022451	chr6:31279535-31485736	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
10	nsv601609	chr6:31280101-31799786	Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
11	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
12	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
13	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
14	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
15	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
16	nsv869722	chr6:31287397-31461074	Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
17	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
18	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
19	nsv517441	chr6:31336100-31463963	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
20	nsv1018463	chr6:31337336-31525275	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	104 gene(s)	inside rSNPs	diseases
21	nsv538189	chr6:31337336-31525275	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	104 gene(s)	inside rSNPs	diseases
22	nsv432868	chr6:31338844-31721033	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer 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	250 gene(s)	inside rSNPs	diseases
23	esv2752115	chr6:31352880-31498721	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
24	esv1831710	chr6:31352945-31477763	Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
25	esv2763959	chr6:31353329-31460220	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
26	nsv1028659	chr6:31353329-31460220	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
27	nsv1034727	chr6:31353329-31465103	Strong transcription Weak transcription Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
28	esv2752118	chr6:31353329-31481321	Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
29	esv2757162	chr6:31353329-31542308	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	99 gene(s)	inside rSNPs	diseases
30	esv1827731	chr6:31353930-31471391	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
31	esv1833123	chr6:31353930-31471391	Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
32	esv1825070	chr6:31354819-31463963	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
33	esv1832352	chr6:31355100-31477763	Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Strong transcription Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
34	nsv601882	chr6:31355318-31461089	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
35	esv3475036	chr6:31356065-31465064	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
36	esv3475037	chr6:31356065-31465064	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
37	esv34684	chr6:31359621-31474688	Flanking Active TSS Weak transcription Genic enhancers Enhancers Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
38	esv2752119	chr6:31359621-31498521	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
39	esv2752121	chr6:31359648-31465795	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
40	nsv1030917	chr6:31360095-31460220	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
41	nsv1021984	chr6:31360095-31465103	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
42	nsv1030071	chr6:31360095-31465795	Enhancers Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
43	nsv1020595	chr6:31360095-31474688	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
44	nsv1022499	chr6:31360095-31485174	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
45	nsv1031110	chr6:31362310-31465103	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
46	nsv1026211	chr6:31362310-31474688	Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Active TSS 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	39 gene(s)	inside rSNPs	diseases
47	nsv1018716	chr6:31362310-31481299	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
48	nsv1031241	chr6:31362930-31460220	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
49	nsv1015252	chr6:31362930-31465103	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
50	esv3434932	chr6:31377226-31471978	Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2904787	CCHCR1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31438200-31461600	Weak transcription	Small Intestine	intestine
2	chr6:31443000-31461600	Weak transcription	Right Atrium	heart
3	chr6:31446200-31461600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr6:31453400-31459800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr6:31453600-31461200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr6:31455400-31460000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr6:31455800-31461400	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr6:31456000-31461600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr6:31456200-31461800	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr6:31457200-31461600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr6:31458000-31461400	Weak transcription	Colonic Mucosa	Colon
12	chr6:31458200-31460200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr6:31458200-31461600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr6:31458400-31461400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr6:31458600-31461200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr6:31458800-31460200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr6:31458800-31461000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr6:31458800-31461200	Weak transcription	Thymus	Thymus
19	chr6:31458800-31461400	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr6:31458800-31461600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr6:31458800-31461600	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr6:31459000-31461400	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr6:31459000-31461600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr6:31459000-31461600	Enhancers	Primary T cells fromperipheralblood	blood
25	chr6:31459200-31461600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr6:31459200-31461600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
27	chr6:31459400-31459800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
28	chr6:31459400-31459800	Flanking Active TSS	Duodenum Mucosa	Duodenum
29	chr6:31459400-31459800	Active TSS	A549	lung
30	chr6:31459400-31460200	Enhancers	Primary T killer memory cells from peripheral blood	blood
31	chr6:31459400-31460200	Flanking Active TSS	K562	blood
32	chr6:31459400-31460600	Enhancers	HMEC	breast
33	chr6:31459400-31461200	Enhancers	Fetal Thymus	thymus
34	chr6:31459400-31461200	Enhancers	HUVEC	blood vessel
35	chr6:31459400-31461400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr6:31459400-31461400	Enhancers	Primary B cells from cord blood	blood
37	chr6:31459400-31461400	Enhancers	Primary T cells from cord blood	blood
38	chr6:31459400-31461400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr6:31459400-31461600	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr6:31459400-31461600	Enhancers	Primary B cells from peripheral blood	blood
41	chr6:31459400-31461600	Enhancers	Primary T helper naive cells from peripheral blood	blood
42	chr6:31459400-31461600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr6:31459400-31461600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr6:31459400-31466600	Active TSS	GM12878-XiMat	blood
45	chr6:31459600-31459800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
46	chr6:31459600-31459800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr6:31459600-31459800	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr6:31459600-31459800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chr6:31459600-31459800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr6:31459600-31459800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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