Variant report

Variant	rs2607015
Chromosome Location	chr6:31762843-31762844
allele	C/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	chr6:31762842-31764771	HepG2	liver:	n/a	n/a
2	POLR2A	chr6:31762366-31764289	MCF-7	breast:	n/a	n/a
3	POLR2A	chr6:31761995-31764710	K562	blood:	n/a	n/a
4	MAX	chr6:31762191-31764152	HepG2	liver:	n/a	chr6:31763488-31763497 chr6:31763485-31763494 chr6:31763486-31763497 chr6:31763489-31763496 chr6:31763487-31763497
5	POLR2A	chr6:31762059-31764086	K562	blood:	n/a	n/a
6	ZBTB7A	chr6:31762354-31764110	ECC-1	luminal epithelium:	n/a	n/a
7	POLR2A	chr6:31762197-31764090	K562	blood:	n/a	n/a
8	POLR2A	chr6:31762741-31764029	H1-hESC	embryonic stem cell:	n/a	n/a
9	YY1	chr6:31762835-31763974	GM12878	blood:	n/a	chr6:31763754-31763763 chr6:31763468-31763482 chr6:31763467-31763481 chr6:31763754-31763768 chr6:31763748-31763762 chr6:31763368-31763382 chr6:31763539-31763548 chr6:31763371-31763385
10	POLR2A	chr6:31762085-31764245	HUVEC	blood vessel:	n/a	n/a
11	TAF1	chr6:31762265-31764119	K562	blood:	n/a	n/a
12	ZMIZ1	chr6:31762092-31764030	K562	blood:	n/a	n/a
13	POLR2A	chr6:31762842-31764116	HepG2	liver:	n/a	n/a
14	ELF1	chr6:31762565-31762986	K562	blood:	n/a	n/a
15	ETS1	chr6:31762362-31764134	K562	blood:	n/a	chr6:31763509-31763526 chr6:31762577-31762588 chr6:31763537-31763548 chr6:31763509-31763526
16	POLR2A	chr6:31762274-31764763	K562	blood:	n/a	n/a
17	POLR2A	chr6:31762136-31765802	SK-N-MC	brain:	n/a	n/a
18	MAX	chr6:31761935-31764190	K562	blood:	n/a	chr6:31763488-31763497 chr6:31763485-31763494 chr6:31763486-31763497 chr6:31763489-31763496 chr6:31763487-31763497
19	GABPA	chr6:31762571-31764055	K562	blood:	n/a	chr6:31763555-31763564 chr6:31763644-31763653
20	YY1	chr6:31762588-31764031	K562	blood:	n/a	chr6:31763754-31763763 chr6:31763468-31763482 chr6:31763467-31763481 chr6:31763754-31763768 chr6:31763748-31763762 chr6:31763368-31763382 chr6:31763539-31763548 chr6:31763371-31763385
21	POLR2A	chr6:31762192-31764199	GM12892	blood:	n/a	n/a
22	POLR2A	chr6:31762671-31764078	NB4	blood:	n/a	n/a
23	POLR2A	chr6:31762386-31764085	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr6:31762659-31764059	GM12891	blood:	n/a	n/a
25	POLR2A	chr6:31762176-31762944	PANC-1	pancreas:	n/a	n/a
26	POLR2A	chr6:31762837-31763572	GM12892	blood:	n/a	n/a
27	CCNT2	chr6:31762037-31762879	K562	blood:	n/a	chr6:31762577-31762586 chr6:31762207-31762227
28	NR2F2	chr6:31761944-31764825	K562	blood:	n/a	n/a
29	POLR2A	chr6:31762018-31764102	K562	blood:	n/a	n/a
30	POLR2A	chr6:31762678-31764164	HL-60	blood:	n/a	n/a
31	BCL3	chr6:31762535-31764219	K562	blood:	n/a	chr6:31763469-31763482 chr6:31763390-31763403 chr6:31763475-31763488 chr6:31763803-31763816 chr6:31763526-31763539
32	SMC3	chr6:31761937-31764138	SK-N-SH	brain:	n/a	n/a
33	TEAD4	chr6:31761914-31763993	K562	blood:	n/a	n/a
34	PML	chr6:31761948-31764253	GM12878	blood:	n/a	n/a
35	POLR2A	chr6:31762532-31764187	MCF-7	breast:	n/a	n/a
36	ZBTB7A	chr6:31762315-31764013	K562	blood:	n/a	n/a
37	HDAC2	chr6:31762318-31764059	K562	blood:	n/a	n/a
38	MTA3	chr6:31762183-31764465	GM12878	blood:	n/a	n/a
39	PML	chr6:31762743-31764434	K562	blood:	n/a	n/a
40	ZBTB7A	chr6:31762466-31762991	HepG2	liver:	n/a	n/a
41	POLR2A	chr6:31762705-31764022	HUVEC	blood vessel:	n/a	n/a
42	CBX3	chr6:31762834-31764422	K562	blood:	n/a	n/a
43	POLR2A	chr6:31762804-31764023	H1-neurons	neurons:	n/a	n/a
44	SIN3AK20	chr6:31761996-31764052	K562	blood:	n/a	n/a
45	ZBTB7A	chr6:31762361-31763975	K562	blood:	n/a	n/a
46	SIN3AK20	chr6:31762440-31762856	H1-hESC	embryonic stem cell:	n/a	n/a
47	MXI1	chr6:31761803-31764149	IMR90	lung:	n/a	n/a
48	POLR2A	chr6:31762361-31764079	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr6:31762252-31764461	GM12878	blood:	n/a	n/a
50	SIN3A	chr6:31762271-31763978	H1-hESC	embryonic stem cell:	n/a	chr6:31763368-31763381 chr6:31763652-31763665

No.	Distal block	Cell Line	Cell type
1	chr6:31761655..31763549-chr6:31865451..31867211,2	MCF-7	breast:
2	chr6:31649204..31651280-chr6:31762211..31763800,2	MCF-7	breast:
3	chr6:31761672..31765296-chr6:31772847..31776146,6	MCF-7	breast:
4	chr6:31760815..31765798-chr6:31772413..31777523,17	MCF-7	breast:
5	chr6:31761456..31762985-chr6:31846516..31848351,2	K562	blood:
6	chr6:31759482..31765185-chr6:31781824..31784897,13	MCF-7	breast:
7	chr6:31620215..31622719-chr6:31761944..31763523,2	MCF-7	breast:
8	chr6:31761659..31764051-chr6:31869423..31871582,3	K562	blood:
9	chr6:31587253..31589657-chr6:31761134..31763419,2	MCF-7	breast:
10	chr6:31762216..31763831-chr6:31854405..31856951,2	MCF-7	breast:
11	chr6:31741149..31744902-chr6:31760858..31763694,5	MCF-7	breast:
12	chr6:31695390..31696984-chr6:31762234..31763768,2	MCF-7	breast:
13	chr6:31619065..31621303-chr6:31762386..31764649,2	MCF-7	breast:
14	chr6:31626696..31628687-chr6:31762053..31764771,3	MCF-7	breast:
15	chr6:31761659..31763884-chr6:31868027..31870923,3	K562	blood:
16	chr6:31758020..31763887-chr6:31863868..31868391,6	K562	blood:
17	chr6:31429705..31431328-chr6:31762595..31764431,2	K562	blood:
18	chr6:31762561..31765176-chr6:31866590..31868817,2	MCF-7	breast:
19	chr17:56594989..56597705-chr6:31762274..31764941,2	MCF-7	breast:
20	chr6:31758502..31767561-chr6:31786193..31804196,52	MCF-7	breast:
21	chr6:31762749..31764673-chr6:32143789..32146313,2	K562	blood:
22	chr6:31684792..31688095-chr6:31761930..31764765,3	MCF-7	breast:
23	chr6:31758631..31763066-chr6:31827655..31831615,4	K562	blood:
24	chr6:31761047..31764270-chr6:31827785..31831725,4	MCF-7	breast:
25	chr6:31667922..31671961-chr6:31761581..31764967,5	MCF-7	breast:
26	chr6:31761963..31763938-chr6:32162269..32164335,2	MCF-7	breast:
27	chr6:31756951..31764627-chr6:31780500..31799197,32	MCF-7	breast:
28	chr6:31685559..31688052-chr6:31762150..31763709,2	MCF-7	breast:
29	chr6:31760851..31764032-chr6:31800769..31804370,7	MCF-7	breast:
30	chr6:31761979..31764717-chr6:31829414..31832230,4	MCF-7	breast:
31	chr6:31706414..31709644-chr6:31760309..31763318,4	MCF-7	breast:
32	chr6:31647614..31649375-chr6:31762314..31763878,2	MCF-7	breast:

Variant related genes	Relation type
VARS	TF binding region
ENSG00000266776	Chromatin interaction
ENSG00000204310	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000255152	Chromatin interaction
ENSG00000204308	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000213654	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000233902	Chromatin interaction
ENSG00000204428	Chromatin interaction
ENSG00000204427	Chromatin interaction
ENSG00000204410	Chromatin interaction
ENSG00000264672	Chromatin interaction
ENSG00000108389	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000213722	Chromatin interaction
ENSG00000204439	Chromatin interaction
ENSG00000204396	Chromatin interaction
ENSG00000206337	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000204469	Chromatin interaction
ENSG00000204420	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000204366	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000204392	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs2075800	0.84[ASN][1000 genomes]
rs2736430	0.84[ASN][1000 genomes]
rs2753960	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9267575	0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	nsv884426	chr6:31728102-31800868	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
14	nsv884427	chr6:31728102-31802465	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers 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 target site	152 gene(s)	inside rSNPs	diseases
15	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
16	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
17	nsv884430	chr6:31731881-31800631	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription 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 lncRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
18	nsv601943	chr6:31733544-31763862	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	55 gene(s)	inside rSNPs	diseases
19	nsv884432	chr6:31734117-31777687	Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
20	nsv884433	chr6:31737701-31777687	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS 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 lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
21	nsv884437	chr6:31739881-31777687	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
22	nsv884440	chr6:31743882-31775984	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
23	nsv884442	chr6:31745518-31764899	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	43 gene(s)	inside rSNPs	diseases
24	nsv884443	chr6:31745518-31777687	Genic enhancers Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
25	nsv601944	chr6:31749541-31763862	Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	40 gene(s)	inside rSNPs	diseases
26	nsv884444	chr6:31756670-31768217	Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	37 gene(s)	inside rSNPs	diseases
27	nsv884445	chr6:31756907-31769250	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	37 gene(s)	inside rSNPs	diseases
28	nsv884446	chr6:31760309-31768971	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	37 gene(s)	inside rSNPs	diseases
29	nsv884447	chr6:31760654-31770770	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	37 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	chr6:31761000-31764000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr6:31761000-31764600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr6:31761200-31764000	Active TSS	GM12878-XiMat	blood
4	chr6:31761400-31764200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr6:31761400-31764400	Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr6:31761600-31763200	Flanking Active TSS	Dnd41	blood
7	chr6:31761800-31763200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
8	chr6:31761800-31764000	Active TSS	HSMMtube	muscle
9	chr6:31761800-31764000	Active TSS	NHLF	lung
10	chr6:31761800-31764200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr6:31761800-31764200	Active TSS	iPS-15b Cell Line	embryonic stem cell
12	chr6:31761800-31764200	Active TSS	Breast Myoepithelial Primary Cells	Breast
13	chr6:31761800-31764400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr6:31762000-31763000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr6:31762000-31763000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
16	chr6:31762000-31763000	Flanking Active TSS	Fetal Brain Male	brain
17	chr6:31762000-31763000	Flanking Active TSS	Right Ventricle	heart
18	chr6:31762000-31763000	Flanking Active TSS	Stomach Smooth Muscle	stomach
19	chr6:31762000-31763200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
20	chr6:31762000-31763400	Flanking Active TSS	Primary B cells from cord blood	blood
21	chr6:31762000-31763400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
22	chr6:31762000-31763400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr6:31762000-31763800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr6:31762000-31764000	Active TSS	H1 Cell Line	embryonic stem cell
25	chr6:31762000-31764000	Flanking Active TSS	Primary hematopoietic stem cells	blood
26	chr6:31762000-31764200	Active TSS	H9 Cell Line	embryonic stem cell
27	chr6:31762000-31764200	Active TSS	Psoas Muscle	Psoas
28	chr6:31762200-31763000	Flanking Active TSS	Primary B cells from peripheral blood	blood
29	chr6:31762200-31763000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr6:31762200-31763000	Flanking Active TSS	Brain Anterior Caudate	brain
31	chr6:31762200-31763000	Flanking Active TSS	Brain Cingulate Gyrus	brain
32	chr6:31762200-31763000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
33	chr6:31762200-31763200	Flanking Active TSS	Brain Substantia Nigra	brain
34	chr6:31762200-31763200	Flanking Active TSS	Fetal Heart	heart
35	chr6:31762200-31763200	Flanking Active TSS	Fetal Muscle Leg	muscle
36	chr6:31762200-31763200	Flanking Active TSS	Fetal Thymus	thymus
37	chr6:31762200-31763200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
38	chr6:31762200-31763400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
39	chr6:31762200-31763400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
40	chr6:31762200-31763400	Flanking Active TSS	Adipose Nuclei	Adipose
41	chr6:31762200-31763400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
42	chr6:31762200-31763400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
43	chr6:31762200-31763600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr6:31762200-31763800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr6:31762200-31763800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
46	chr6:31762200-31763800	Active TSS	Muscle Satellite Cultured Cells	--
47	chr6:31762200-31763800	Active TSS	NHEK	skin
48	chr6:31762200-31764000	Active TSS	ES-I3 Cell Line	embryonic stem cell
49	chr6:31762200-31764000	Active TSS	HUES48 Cell Line	embryonic stem cell
50	chr6:31762200-31764000	Active TSS	HUES6 Cell Line	embryonic stem cell

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