Variant report

Variant	rs17207713
Chromosome Location	chr6:31833221-31833222
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:79)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:79 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOXA1	chr6:31832996-31833589	HepG2	liver:	n/a	n/a
2	MBD4	chr6:31832901-31833804	HepG2	liver:	n/a	n/a
3	TEAD4	chr6:31832802-31833978	HepG2	liver:	n/a	n/a
4	POLR2A	chr6:31832294-31833670	HepG2	liver:	n/a	n/a
5	YY1	chr6:31832941-31833439	HepG2	liver:	n/a	chr6:31833149-31833166
6	HNF4G	chr6:31832923-31833774	HepG2	liver:	n/a	chr6:31833173-31833186 chr6:31833173-31833187 chr6:31833228-31833242 chr6:31833226-31833244 chr6:31833169-31833191 chr6:31833229-31833241 chr6:31833172-31833187 chr6:31833229-31833242 chr6:31833229-31833241
7	NR2F2	chr6:31833016-31833352	K562	blood:	n/a	n/a
8	POLR2A	chr6:31832801-31833645	HepG2	liver:	n/a	n/a
9	MYBL2	chr6:31832778-31833746	HepG2	liver:	n/a	n/a
10	MAX	chr6:31832899-31833626	HepG2	liver:	n/a	n/a
11	POLR2A	chr6:31832664-31833961	HepG2	liver:	n/a	n/a
12	CHD2	chr6:31832931-31833686	HepG2	liver:	n/a	chr6:31833075-31833085
13	YY1	chr6:31832769-31833525	HepG2	liver:	n/a	chr6:31833149-31833166
14	CEBPB	chr6:31833012-31833608	HepG2	liver:	n/a	n/a
15	USF1	chr6:31833071-31833503	HepG2	liver:	n/a	n/a
16	FOXA1	chr6:31832946-31833595	HepG2	liver:	n/a	n/a
17	BHLHE40	chr6:31832970-31833542	HepG2	liver:	n/a	n/a
18	JUND	chr6:31832999-31833590	HepG2	liver:	n/a	chr6:31833071-31833080
19	RAD21	chr6:31832992-31833521	HepG2	liver:	n/a	n/a
20	RCOR1	chr6:31832549-31834019	HepG2	liver:	n/a	n/a
21	CEBPB	chr6:31833121-31833308	HepG2	liver:	n/a	n/a
22	MAFF	chr6:31832924-31833401	HepG2	liver:	n/a	n/a
23	HDAC2	chr6:31832680-31834128	HepG2	liver:	n/a	n/a
24	POLR2A	chr6:31832939-31833507	HepG2	liver:	n/a	n/a
25	ELF1	chr6:31833048-31833413	HepG2	liver:	n/a	n/a
26	CTCF	chr6:31833100-31833250	Caco-2	colon:	n/a	n/a
27	POLR2A	chr6:31832263-31834177	HepG2	liver:	n/a	n/a
28	RAD21	chr6:31832922-31833676	HepG2	liver:	n/a	n/a
29	RFX5	chr6:31833159-31833358	HepG2	liver:	n/a	n/a
30	HNF4A	chr6:31832926-31833660	HepG2	liver:	n/a	chr6:31833173-31833186 chr6:31833173-31833187 chr6:31833228-31833242 chr6:31833226-31833244 chr6:31833227-31833242 chr6:31833169-31833191 chr6:31833229-31833241 chr6:31833172-31833187 chr6:31833229-31833242 chr6:31833229-31833241
31	SP1	chr6:31832827-31833655	HepG2	liver:	n/a	n/a
32	HNF4A	chr6:31832957-31833698	HepG2	liver:	n/a	chr6:31833173-31833186 chr6:31833173-31833187 chr6:31833228-31833242 chr6:31833226-31833244 chr6:31833227-31833242 chr6:31833169-31833191 chr6:31833229-31833241 chr6:31833172-31833187 chr6:31833229-31833242 chr6:31833229-31833241
33	ARID3A	chr6:31832848-31833544	HepG2	liver:	n/a	n/a
34	SRF	chr6:31832889-31833556	HepG2	liver:	n/a	chr6:31833147-31833162
35	CEBPD	chr6:31832710-31833469	HepG2	liver:	n/a	n/a
36	TEAD4	chr6:31832923-31833345	K562	blood:	n/a	n/a
37	RAD21	chr6:31832910-31833586	HepG2	liver:	n/a	n/a
38	JUN	chr6:31832994-31833453	HepG2	liver:	n/a	chr6:31833071-31833080
39	POLR2A	chr6:31832652-31833620	HepG2	liver:	n/a	n/a
40	NR2F2	chr6:31832744-31833720	HepG2	liver:	n/a	n/a
41	CTCF	chr6:31833044-31833456	HepG2	liver:	n/a	n/a
42	EP300	chr6:31832740-31833821	HepG2	liver:	n/a	n/a
43	FOXA1	chr6:31832921-31833482	HepG2	liver:	n/a	n/a
44	ZBTB7A	chr6:31832988-31833371	HepG2	liver:	n/a	n/a
45	EP300	chr6:31832981-31833735	HepG2	liver:	n/a	n/a
46	BRCA1	chr6:31832911-31833563	HepG2	liver:	n/a	n/a
47	HEY1	chr6:31832079-31834004	HepG2	liver:	n/a	n/a
48	JUN	chr6:31829065-31833596	K562	blood:	n/a	chr6:31833071-31833080 chr6:31830957-31830966 chr6:31830955-31830967 chr6:31830385-31830394 chr6:31830953-31830964 chr6:31830860-31830869
49	REST	chr6:31832986-31833407	HepG2	liver:	n/a	n/a
50	POLR2A	chr6:31832338-31833713	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31833199-31833249	PANC-1	pancreas:	n/a
2	chr6:31833199-31833249	MCF-7	breast:	n/a
3	chr6:31833199-31833249	Hela-S3	cervix:	n/a
4	chr6:31833199-31833249	PrEC	prostate:	n/a
5	chr6:31833199-31833249	NH-A	brain:	n/a
6	chr6:31833199-31833249	Jurkat	blood:	n/a
7	chr6:31833199-31833249	HCPEpiC	choroid plexus:	n/a
8	chr6:31833199-31833249	GM12891	blood:	n/a
9	chr6:31833199-31833249	LNCaP	prostate:	n/a
10	chr6:31833199-31833249	GM12878	blood:	n/a
11	chr6:31833199-31833249	HIPEpiC	eye:	n/a
12	chr6:31833199-31833249	SK-N-SH	brain:	n/a
13	chr6:31833199-31833249	AG04450	lung:	fetal
14	chr6:31833199-31833249	NT2-D1	testis:	n/a
15	chr6:31833199-31833249	HCF	heart:	n/a
16	chr6:31833199-31833249	ProgFib	skin:	n/a
17	chr6:31833199-31833249	HRPEpiC	eye:	n/a
18	chr6:31833199-31833249	ovcar-3	ovarian:	n/a
19	chr6:31833199-31833249	SAEC	small airway:	n/a
20	chr6:31833199-31833249	NB4	blood:	n/a
21	chr6:31833199-31833249	AG10803	skin:	n/a
22	chr6:31833199-31833249	IMR90	lung:	fetal
23	chr6:31833199-31833249	GM19239	blood:	n/a
24	chr6:31833199-31833249	AG04449	skin:	fetal
25	chr6:31833199-31833249	SKMC	muscle:	n/a
26	chr6:31833199-31833249	A549	lung:	n/a
27	chr6:31833199-31833249	HMEC	breast:	n/a
28	chr6:31833199-31833249	HL-60	blood:	n/a
29	chr6:31833199-31833249	U87	brain:	n/a
30	chr6:31833199-31833249	HPAEpiC	pulmonary alveolar:	n/a
31	chr6:31833199-31833249	HEEpiC	esophagus:	n/a
32	chr6:31833199-31833249	SK-N-MC	brain:	n/a
33	chr6:31833199-31833249	RPTEC	kidney:	n/a
34	chr6:31833199-31833249	HUVEC	blood vessel:	n/a
35	chr6:31833199-31833249	ECC-1	luminal epithelium:	n/a
36	chr6:31833199-31833249	GM06990	blood:	n/a
37	chr6:31833199-31833249	HRCEpiC	kidney:	n/a
38	chr6:31833199-31833249	Caco-2	colon:	n/a
39	chr6:31833199-31833249	HEK293	kidney:	embryo
40	chr6:31833199-31833249	BE2_C	brain:	n/a
41	chr6:31833199-31833249	HAEpiC	amniotic membrane:	n/a
42	chr6:31833199-31833249	AG09319	gingival:	n/a
43	chr6:31833199-31833249	MCF10A-Er-Src	breast:	n/a
44	chr6:31833199-31833249	NHDF-neo	bronchial:	n/a
45	chr6:31833199-31833249	H1-hESC	embryonic stem cell:	embryo
46	chr6:31833199-31833249	HCM	heart:	n/a
47	chr6:31833199-31833249	Hepatocyte	liver:	n/a
48	chr6:31833199-31833249	K562	blood:	n/a
49	chr6:31833199-31833249	AG09309	skin:	n/a
50	chr6:31833199-31833249	NHBE	bronchial:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31830912..31833686-chr6:32013315..32015593,2	K562	blood:
2	chr6:31829055..31832274-chr6:31832876..31835978,7	MCF-7	breast:
3	chr6:31670174..31672313-chr6:31830988..31833810,3	K562	blood:
4	chr6:31774180..31776496-chr6:31832190..31834757,3	K562	blood:
5	chr6:31772422..31776496-chr6:31829254..31834757,6	K562	blood:
6	chr6:31832130..31834569-chr6:31860075..31862005,2	K562	blood:
7	chr6:31691508..31694089-chr6:31833042..31835774,2	K562	blood:
8	chr6:31630209..31635577-chr6:31828786..31834874,28	K562	blood:
9	chr6:31830083..31833987-chr6:31862759..31865610,4	MCF-7	breast:
10	chr6:31800580..31812447-chr6:31823435..31837480,47	K562	blood:
11	chr6:31801090..31813654-chr6:31824519..31834411,41	MCF-7	breast:
12	chr6:31630694..31635339-chr6:31828920..31834068,22	K562	blood:
13	chr6:31617566..31630444-chr6:31823885..31836000,84	K562	blood:
14	chr6:31831274..31833961-chr6:31853684..31856241,2	K562	blood:
15	chr6:31828958..31833712-chr6:31836982..31839801,4	MCF-7	breast:
16	chr6:31729872..31732091-chr6:31831679..31833339,2	K562	blood:
17	chr6:31800755..31815108-chr6:31823340..31833266,54	K562	blood:
18	chr6:31793612..31800139-chr6:31830250..31833240,9	K562	blood:
19	chr6:31586339..31592286-chr6:31830032..31833457,6	K562	blood:
20	chr6:31617566..31622844-chr6:31826455..31835211,65	K562	blood:

No data

Variant related genes	Relation type
NEU1	TF binding region
SLC44A4	TF binding region
NEU1	CpG island
SLC44A4	CpG island
ENSG00000201754	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000168477	Chromatin interaction
ENSG00000204427	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000204392	Chromatin interaction
ENSG00000228727	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000227198	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000201207	Chromatin interaction
ENSG00000255152	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000204469	Chromatin interaction
ENSG00000204439	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000200816	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs17201227	0.88[AFR][1000 genomes]
rs17201269	0.88[AFR][1000 genomes]
rs17207608	0.88[AFR][1000 genomes]
rs17207657	0.88[AFR][1000 genomes]
rs61745377	1.00[AFR][1000 genomes]
rs6908775	0.88[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

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	nsv884429	chr6:31730356-31837066	Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	155 gene(s)	inside rSNPs	diseases
14	nsv462872	chr6:31778272-31864304	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
15	nsv601945	chr6:31778272-31864304	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
16	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
17	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
18	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
19	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
20	nsv462874	chr6:31794592-31864304	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
21	nsv601959	chr6:31794592-31864304	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
22	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
23	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

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31830800-31845200	Weak transcription	Small Intestine	intestine
2	chr6:31831000-31834200	Genic enhancers	Stomach Mucosa	stomach
3	chr6:31831800-31833400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:31831800-31834000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:31831800-31845000	Weak transcription	Lung	lung
6	chr6:31832000-31833800	Enhancers	Liver	Liver
7	chr6:31832000-31835200	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr6:31832000-31842600	Strong transcription	Colonic Mucosa	Colon
9	chr6:31832000-31856000	Weak transcription	Right Atrium	heart
10	chr6:31832200-31833800	Enhancers	Fetal Muscle Trunk	muscle
11	chr6:31832200-31833800	Weak transcription	Rectal Smooth Muscle	rectum
12	chr6:31832200-31834000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:31832200-31834000	Enhancers	Placenta	Placenta
14	chr6:31832200-31842800	Strong transcription	Fetal Intestine Small	intestine
15	chr6:31832400-31833400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr6:31832400-31833400	Strong transcription	Fetal Intestine Large	intestine
17	chr6:31832400-31833400	Enhancers	A549	lung
18	chr6:31832400-31833400	Enhancers	Hela-S3	cervix
19	chr6:31832400-31834000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr6:31832400-31835800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr6:31832400-31836000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr6:31832400-31836600	Weak transcription	Pancreas	Pancrea
23	chr6:31832400-31838400	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr6:31832400-31838600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr6:31832400-31840000	Strong transcription	Sigmoid Colon	Sigmoid Colon
26	chr6:31832400-31840600	Strong transcription	Rectal Mucosa Donor 29	rectum
27	chr6:31832400-31840600	Strong transcription	Rectal Mucosa Donor 31	rectum
28	chr6:31832400-31847400	Weak transcription	Primary T helper cells PMA-I stimulated	--
29	chr6:31832400-31847600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr6:31832400-31847600	Weak transcription	NH-A	brain
31	chr6:31832400-31848200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr6:31832400-31850800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr6:31832600-31833600	Strong transcription	Gastric	stomach
34	chr6:31832600-31833800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr6:31832600-31833800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr6:31832600-31834000	Weak transcription	Stomach Smooth Muscle	stomach
37	chr6:31832600-31834200	Strong transcription	Fetal Stomach	stomach
38	chr6:31832600-31838000	Weak transcription	Spleen	Spleen
39	chr6:31832600-31838200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr6:31832800-31833400	Bivalent/Poised TSS	HepG2	liver
41	chr6:31832800-31833600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr6:31833000-31833400	Enhancers	Dnd41	blood
43	chr6:31833000-31833600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr6:31833000-31834000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr6:31833000-31838600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr6:31833000-31847400	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr6:31833200-31833400	Enhancers	H1 Cell Line	embryonic stem cell
48	chr6:31833200-31833800	Genic enhancers	K562	blood
49	chr6:31833200-31834200	Strong transcription	Duodenum Mucosa	Duodenum
50	chr6:31833200-31836600	Weak transcription	Fetal Thymus	thymus

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