Variant report

Variant	rs17201466
Chromosome Location	chr6:31926600-31926601
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:390)
CpG islands
(count:244)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:390 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:31926448-31927155	Hela-S3	cervix:	n/a	n/a
2	EP300	chr6:31926589-31927245	K562	blood:	n/a	chr6:31926869-31926876
3	POU2F2	chr6:31926417-31927249	GM12878	blood:	n/a	chr6:31926828-31926840
4	ELF1	chr6:31926369-31927344	K562	blood:	n/a	chr6:31926932-31926945 chr6:31926864-31926877 chr6:31926867-31926876
5	KAP1	chr6:31926571-31927246	HEK293	kidney:	n/a	n/a
6	UBTF	chr6:31926534-31927187	K562	blood:	n/a	n/a
7	YY1	chr6:31926511-31927147	SK-N-SH_RA	brain:	n/a	chr6:31926996-31927007
8	JUND	chr6:31926531-31927226	K562	blood:	n/a	n/a
9	TAF1	chr6:31926592-31927220	HepG2	liver:	n/a	n/a
10	POLR2A	chr6:31926315-31927314	GM12892	blood:	n/a	n/a
11	CREB1	chr6:31926561-31927083	A549	lung:	n/a	n/a
12	POLR2A	chr6:31926273-31927396	HUVEC	blood vessel:	n/a	n/a
13	E2F4	chr6:31926565-31927203	K562	blood:	n/a	n/a
14	POLR2A	chr6:31926508-31927175	K562	blood:	n/a	n/a
15	SP4	chr6:31926330-31927077	H1-hESC	embryonic stem cell:	n/a	chr6:31926897-31926908
16	POLR2A	chr6:31926430-31927297	GM12878	blood:	n/a	n/a
17	MAX	chr6:31926325-31927293	A549	lung:	n/a	n/a
18	SIX5	chr6:31926544-31927079	A549	lung:	n/a	n/a
19	ATF1	chr6:31926331-31927215	K562	blood:	n/a	n/a
20	SIN3AK20	chr6:31926568-31927175	A549	lung:	n/a	n/a
21	CUX1	chr6:31926476-31927146	GM12878	blood:	n/a	n/a
22	SP4	chr6:31926501-31927215	H1-hESC	embryonic stem cell:	n/a	chr6:31926897-31926908
23	GABPA	chr6:31926167-31927372	A549	lung:	n/a	n/a
24	POLR2A	chr6:31926218-31927259	MCF-7	breast:	n/a	n/a
25	SIN3AK20	chr6:31926452-31927184	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr6:31926495-31927178	GM15510	blood:	n/a	n/a
27	MAX	chr6:31926287-31927262	NB4	blood:	n/a	n/a
28	NFIC	chr6:31926455-31927169	GM12878	blood:	n/a	n/a
29	IRF1	chr6:31926580-31927250	K562	blood:	n/a	n/a
30	ZEB1	chr6:31926477-31927033	GM12878	blood:	n/a	n/a
31	TAF1	chr6:31926439-31927276	GM12878	blood:	n/a	n/a
32	POLR2A	chr6:31926489-31927275	MCF-7	breast:	n/a	n/a
33	SRF	chr6:31926495-31927108	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr6:31926482-31927344	HepG2	liver:	n/a	n/a
35	SRF	chr6:31926546-31927025	GM12878	blood:	n/a	n/a
36	SRF	chr6:31926597-31927061	HepG2	liver:	n/a	n/a
37	MAX	chr6:31926577-31927197	A549	lung:	n/a	n/a
38	POLR2A	chr6:31926519-31927159	U87	brain:	n/a	n/a
39	POLR2A	chr6:31926585-31927207	Gliobla	brain:	n/a	n/a
40	POLR2A	chr6:31926458-31927207	NB4	blood:	n/a	n/a
41	ELF1	chr6:31926526-31927397	HepG2	liver:	n/a	chr6:31926932-31926945 chr6:31926864-31926877 chr6:31926867-31926876
42	CREB1	chr6:31926122-31927508	HepG2	liver:	n/a	n/a
43	ETS1	chr6:31926560-31927105	GM12878	blood:	n/a	chr6:31926868-31926877 chr6:31926869-31926879 chr6:31926868-31926877 chr6:31926868-31926877 chr6:31926868-31926877 chr6:31926994-31927005 chr6:31926865-31926878 chr6:31926868-31926877 chr6:31926868-31926877 chr6:31926864-31926880
44	POLR2A	chr6:31926599-31926828	A549	lung:	n/a	n/a
45	YY1	chr6:31926525-31927136	GM12892	blood:	n/a	chr6:31926996-31927007
46	SIX5	chr6:31926569-31927118	K562	blood:	n/a	n/a
47	YY1	chr6:31926331-31927255	HepG2	liver:	n/a	chr6:31926996-31927007
48	POLR2A	chr6:31926520-31927272	Hela-S3	cervix:	n/a	n/a
49	ARID3A	chr6:31926577-31927188	HepG2	liver:	n/a	n/a
50	MAX	chr6:31926419-31927162	SK-N-SH	brain:	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	chr6:31926586-31926636	HRPEpiC	eye:	n/a
2	chr6:31926586-31926636	GM12892	blood:	n/a
3	chr6:31926586-31926636	HIPEpiC	eye:	n/a
4	chr6:31926586-31926636	A549	lung:	n/a
5	chr6:31926590-31926640	GM12878	blood:	n/a
6	chr6:31926569-31926619	AoSMC	blood vessel:	n/a
7	chr6:31926586-31926636	H1-hESC	embryonic stem cell:	embryo
8	chr6:31926581-31926631	MCF10A-Er-Src	breast:	n/a
9	chr6:31926569-31926619	HCM	heart:	n/a
10	chr6:31926569-31926619	MCF-7	breast:	n/a
11	chr6:31926586-31926636	LNCaP	prostate:	n/a
12	chr6:31926590-31926640	NT2-D1	testis:	n/a
13	chr6:31926581-31926631	LNCaP	prostate:	n/a
14	chr6:31926581-31926631	HNPCEpiC	eye:	n/a
15	chr6:31926569-31926619	HCPEpiC	choroid plexus:	n/a
16	chr6:31926581-31926631	Hepatocyte	liver:	n/a
17	chr6:31926569-31926619	IMR90	lung:	fetal
18	chr6:31926586-31926636	SK-N-SH	brain:	n/a
19	chr6:31926569-31926619	GM06990	blood:	n/a
20	chr6:31926590-31926640	HUVEC	blood vessel:	n/a
21	chr6:31926569-31926619	ProgFib	skin:	n/a
22	chr6:31926590-31926640	NB4	blood:	n/a
23	chr6:31926586-31926636	HPAEpiC	pulmonary alveolar:	n/a
24	chr6:31926590-31926640	HCPEpiC	choroid plexus:	n/a
25	chr6:31926581-31926631	ECC-1	luminal epithelium:	n/a
26	chr6:31926586-31926636	HCF	heart:	n/a
27	chr6:31926581-31926631	HRPEpiC	eye:	n/a
28	chr6:31926569-31926619	HEK293	kidney:	embryo
29	chr6:31926586-31926636	HMEC	breast:	n/a
30	chr6:31926569-31926619	K562	blood:	n/a
31	chr6:31926586-31926636	T-47D	breast:	n/a
32	chr6:31926581-31926631	HPAEpiC	pulmonary alveolar:	n/a
33	chr6:31926581-31926631	PFSK-1	brain:	n/a
34	chr6:31926569-31926619	HAEpiC	amniotic membrane:	n/a
35	chr6:31926590-31926640	U87	brain:	n/a
36	chr6:31926581-31926631	PANC-1	pancreas:	n/a
37	chr6:31926581-31926631	SK-N-SH_RA	brain:	n/a
38	chr6:31926586-31926636	NH-A	brain:	n/a
39	chr6:31926569-31926619	BJ	skin:	n/a
40	chr6:31926586-31926636	AG09319	gingival:	n/a
41	chr6:31926581-31926631	MCF-7	breast:	n/a
42	chr6:31926569-31926619	RPTEC	kidney:	n/a
43	chr6:31926586-31926636	SK-N-SH_RA	brain:	n/a
44	chr6:31926590-31926640	Hepatocyte	liver:	n/a
45	chr6:31926569-31926619	AG04449	skin:	fetal
46	chr6:31926586-31926636	Hela-S3	cervix:	n/a
47	chr6:31926586-31926636	U87	brain:	n/a
48	chr6:31926586-31926636	NHDF-neo	bronchial:	n/a
49	chr6:31926590-31926640	H1-hESC	embryonic stem cell:	embryo
50	chr6:31926590-31926640	AG09319	gingival:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31781796..31783894-chr6:31925428..31927086,2	K562	blood:
2	chr6:31634033..31636196-chr6:31925448..31927170,2	K562	blood:
3	chr6:31844767..31847605-chr6:31925658..31928567,2	MCF-7	breast:
4	chr6:31862879..31872535-chr6:31911667..31928766,47	MCF-7	breast:
5	chr6:31830490..31833199-chr6:31923802..31927860,4	MCF-7	breast:
6	chr6:31864040..31872511-chr6:31917614..31930102,27	MCF-7	breast:
7	chr6:31864712..31866806-chr6:31924793..31927734,3	K562	blood:
8	chr6:31894560..31897888-chr6:31924484..31928410,3	K562	blood:
9	chr6:31829193..31831687-chr6:31925120..31927788,2	MCF-7	breast:
10	chr6:31799457..31804164-chr6:31924693..31928301,4	K562	blood:
11	chr6:31632061..31634821-chr6:31925160..31927798,3	MCF-7	breast:
12	chr6:31654964..31657960-chr6:31926410..31928172,2	K562	blood:
13	chr6:31867895..31873109-chr6:31925613..31930389,7	K562	blood:
14	chr6:31800973..31803192-chr6:31924804..31927036,2	MCF-7	breast:
15	chr6:31925015..31926680-chr6:32161987..32163956,2	K562	blood:
16	chr6:31894560..31897888-chr6:31924484..31926934,4	K562	blood:
17	chr6:31742931..31744824-chr6:31926408..31928564,2	K562	blood:

No data

Variant related genes	Relation type
MIR1236	TF binding region
SKIV2L	TF binding region
NELFE	TF binding region
NELFE	CpG island
SKIV2L	CpG island
MIR1236	CpG island
ENSG00000204371	Chromatin interaction
ENSG00000204396	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000244255	Chromatin interaction
ENSG00000204366	Chromatin interaction
ENSG00000204427	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000213654	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000166278	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs11576014	1.00[ASN][1000 genomes]
rs17201046	1.00[AFR][1000 genomes]
rs41270450	1.00[AFR][1000 genomes]
rs61745355	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 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	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
9	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
10	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
11	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
12	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
13	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
14	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
15	nsv427751	chr6:31871512-32092843	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
16	nsv428141	chr6:31871512-32092843	Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
17	esv2758043	chr6:31871512-32209113	Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
18	esv2759415	chr6:31871512-32209113	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
19	nsv830628	chr6:31887554-31947600	Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	69 gene(s)	inside rSNPs	diseases
20	nsv933250	chr6:31905060-32008005	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' 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	76 gene(s)	inside rSNPs	diseases
21	nsv934279	chr6:31905060-32013902	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
22	nsv884512	chr6:31908470-31933161	Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	44 gene(s)	inside rSNPs	diseases
23	nsv884513	chr6:31922575-32066025	Bivalent Enhancer Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
24	nsv884514	chr6:31923052-31958960	Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Weak transcription Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
25	nsv932869	chr6:31924496-32013902	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
26	nsv933913	chr6:31924682-32009282	Active TSS Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
27	nsv284	chr6:31925739-31996721	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
28	nsv5247	chr6:31925739-32023216	Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription 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 miRNA target site	64 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:148 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31925600-31926600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
2	chr6:31925600-31927800	Active TSS	HUES64 Cell Line	embryonic stem cell
3	chr6:31925800-31926600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
4	chr6:31925800-31926600	Flanking Active TSS	Primary B cells from cord blood	blood
5	chr6:31925800-31926600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
6	chr6:31925800-31926600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
7	chr6:31925800-31926600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr6:31925800-31926600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr6:31925800-31926600	Flanking Active TSS	Adipose Nuclei	Adipose
10	chr6:31925800-31926600	Flanking Active TSS	Liver	Liver
11	chr6:31925800-31926600	Flanking Active TSS	Stomach Smooth Muscle	stomach
12	chr6:31925800-31926600	Flanking Active TSS	Thymus	Thymus
13	chr6:31925800-31927200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr6:31925800-31927200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr6:31925800-31927200	Active TSS	NHDF-Ad	bronchial
16	chr6:31925800-31927400	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr6:31925800-31927400	Active TSS	Psoas Muscle	Psoas
18	chr6:31926000-31926600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
19	chr6:31926000-31926600	Flanking Active TSS	Primary B cells from peripheral blood	blood
20	chr6:31926000-31926600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
21	chr6:31926000-31926600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
22	chr6:31926000-31926600	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr6:31926000-31926600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
24	chr6:31926000-31926600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
25	chr6:31926000-31926600	Flanking Active TSS	Pancreas	Pancrea
26	chr6:31926000-31926600	Flanking Active TSS	Sigmoid Colon	Sigmoid Colon
27	chr6:31926000-31926800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
28	chr6:31926000-31927200	Active TSS	Fetal Intestine Large	intestine
29	chr6:31926000-31927400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr6:31926000-31927600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr6:31926000-31927600	Active TSS	HUES48 Cell Line	embryonic stem cell
32	chr6:31926000-31927800	Active TSS	HUES6 Cell Line	embryonic stem cell
33	chr6:31926000-31927800	Active TSS	A549	lung
34	chr6:31926200-31927000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr6:31926200-31927000	Active TSS	Fetal Brain Female	brain
36	chr6:31926200-31927000	Active TSS	Fetal Heart	heart
37	chr6:31926200-31927000	Active TSS	Fetal Intestine Small	intestine
38	chr6:31926200-31927000	Active TSS	Fetal Lung	lung
39	chr6:31926200-31927000	Active TSS	Rectal Smooth Muscle	rectum
40	chr6:31926200-31927000	Active TSS	K562	blood
41	chr6:31926200-31927000	Active TSS	NH-A	brain
42	chr6:31926200-31927000	Active TSS	Osteobl	bone
43	chr6:31926200-31927200	Active TSS	H9 Cell Line	embryonic stem cell
44	chr6:31926200-31927200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr6:31926200-31927200	Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr6:31926200-31927200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
47	chr6:31926200-31927200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr6:31926200-31927200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr6:31926200-31927200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr6:31926200-31927200	Active TSS	Brain Anterior Caudate	brain

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