Variant report

Variant	rs138074588
Chromosome Location	chr6:31760763-31760764
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:34)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:34 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	USF1	chr6:31760450-31760807	SK-N-SH	brain:	n/a	n/a
2	USF2	chr6:31760481-31760804	Hela-S3	cervix:	n/a	chr6:31760611-31760622
3	MAX	chr6:31760277-31761146	HCT-116	colon:	n/a	chr6:31760403-31760413
4	CTCF	chr6:31760620-31760770	HCFaa	heart:	n/a	n/a
5	POLR2A	chr6:31760571-31760841	MCF10A-Er-Src	breast:	n/a	n/a
6	POLR2A	chr6:31760438-31761056	HCT-116	colon:	n/a	n/a
7	MAX	chr6:31760314-31761145	HCT-116	colon:	n/a	chr6:31760403-31760413
8	USF1	chr6:31760214-31761054	HCT-116	colon:	n/a	n/a
9	POLR2A	chr6:31760747-31760764	Gliobla	brain:	n/a	n/a
10	YY1	chr6:31760539-31760856	HCT-116	colon:	n/a	n/a
11	POLR2A	chr6:31760513-31760880	Hela-S3	cervix:	n/a	n/a
12	POLR2A	chr6:31760067-31760811	K562	blood:	n/a	n/a
13	FOS	chr6:31760541-31760898	MCF10A-Er-Src	breast:	n/a	chr6:31760753-31760762
14	FOS	chr6:31760510-31760922	MCF10A-Er-Src	breast:	n/a	chr6:31760753-31760762
15	CTCF	chr6:31760700-31760850	HBMEC	blood vessel:	n/a	n/a
16	FOSL2	chr6:31760403-31761008	SK-N-SH	brain:	n/a	chr6:31760753-31760762
17	POLR2A	chr6:31760390-31760950	HCT-116	colon:	n/a	n/a
18	POLR2A	chr6:31760564-31760846	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr6:31760541-31760909	MCF10A-Er-Src	breast:	n/a	chr6:31760753-31760762
20	POLR2A	chr6:31760591-31760809	HUVEC	blood vessel:	n/a	n/a
21	ZBTB7A	chr6:31760681-31760924	K562	blood:	n/a	n/a
22	STAT3	chr6:31760567-31760844	MCF10A-Er-Src	breast:	n/a	n/a
23	POLR2A	chr6:31760595-31760863	U87	brain:	n/a	n/a
24	STAT3	chr6:31760493-31760853	MCF10A-Er-Src	breast:	n/a	n/a
25	POLR2A	chr6:31759184-31761108	K562	blood:	n/a	n/a
26	STAT3	chr6:31760598-31760774	MCF10A-Er-Src	breast:	n/a	n/a
27	MYC	chr6:31760540-31760889	MCF10A-Er-Src	breast:	n/a	n/a
28	USF1	chr6:31760291-31761141	HCT-116	colon:	n/a	n/a
29	MYC	chr6:31760474-31760848	MCF10A-Er-Src	breast:	n/a	n/a
30	GABPA	chr6:31760434-31760870	SK-N-SH	brain:	n/a	n/a
31	USF1	chr6:31760428-31760784	SK-N-SH_RA	brain:	n/a	n/a
32	RAD21	chr6:31760650-31760836	Hela-S3	cervix:	n/a	n/a
33	FOS	chr6:31760509-31760909	MCF10A-Er-Src	breast:	n/a	chr6:31760753-31760762
34	USF1	chr6:31760472-31760763	SK-N-SH_RA	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31760762-31760812	HCT-116	colon:	n/a
2	chr6:31760762-31760812	U87	brain:	n/a
3	chr6:31760762-31760812	PrEC	prostate:	n/a
4	chr6:31760762-31760812	GM12891	blood:	n/a
5	chr6:31760762-31760812	HEK293	kidney:	embryo
6	chr6:31760762-31760812	HepG2	liver:	n/a
7	chr6:31760762-31760812	HRPEpiC	eye:	n/a
8	chr6:31760762-31760812	SAEC	small airway:	n/a
9	chr6:31760762-31760812	ovcar-3	ovarian:	n/a
10	chr6:31760762-31760812	HCPEpiC	choroid plexus:	n/a
11	chr6:31760762-31760812	Hepatocyte	liver:	n/a
12	chr6:31760762-31760812	IMR90	lung:	fetal
13	chr6:31760762-31760812	K562	blood:	n/a
14	chr6:31760762-31760812	H1-hESC	embryonic stem cell:	embryo
15	chr6:31760762-31760812	LNCaP	prostate:	n/a
16	chr6:31760762-31760812	HL-60	blood:	n/a
17	chr6:31760762-31760812	HAEpiC	amniotic membrane:	n/a
18	chr6:31760762-31760812	A549	lung:	n/a
19	chr6:31760762-31760812	ProgFib	skin:	n/a
20	chr6:31760762-31760812	Caco-2	colon:	n/a
21	chr6:31760762-31760812	AoSMC	blood vessel:	n/a
22	chr6:31760762-31760812	SK-N-SH_RA	brain:	n/a
23	chr6:31760762-31760812	GM19239	blood:	n/a
24	chr6:31760762-31760812	PFSK-1	brain:	n/a
25	chr6:31760762-31760812	AG04450	lung:	fetal
26	chr6:31760762-31760812	SK-N-SH	brain:	n/a
27	chr6:31760762-31760812	T-47D	breast:	n/a
28	chr6:31760762-31760812	RPTEC	kidney:	n/a
29	chr6:31760762-31760812	PANC-1	pancreas:	n/a
30	chr6:31760762-31760812	GM06990	blood:	n/a
31	chr6:31760762-31760812	AG04449	skin:	fetal
32	chr6:31760762-31760812	NB4	blood:	n/a
33	chr6:31760762-31760812	HNPCEpiC	eye:	n/a
34	chr6:31760762-31760812	SKMC	muscle:	n/a
35	chr6:31760762-31760812	HCF	heart:	n/a
36	chr6:31760762-31760812	HMEC	breast:	n/a
37	chr6:31760762-31760812	GM12878	blood:	n/a
38	chr6:31760762-31760812	MCF10A-Er-Src	breast:	n/a
39	chr6:31760762-31760812	ECC-1	luminal epithelium:	n/a
40	chr6:31760762-31760812	Jurkat	blood:	n/a
41	chr6:31760762-31760812	HPAEpiC	pulmonary alveolar:	n/a
42	chr6:31760762-31760812	HEEpiC	esophagus:	n/a
43	chr6:31760762-31760812	NH-A	brain:	n/a
44	chr6:31760762-31760812	GM12892	blood:	n/a
45	chr6:31760762-31760812	AG09319	gingival:	n/a
46	chr6:31760762-31760812	HUVEC	blood vessel:	n/a
47	chr6:31760762-31760812	NHBE	bronchial:	n/a
48	chr6:31760762-31760812	AG10803	skin:	n/a
49	chr6:31760762-31760812	CMK	blood:	n/a
50	chr6:31760762-31760812	Hela-S3	cervix:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31759482..31765185-chr6:31781824..31784897,13	MCF-7	breast:
2	chr6:31702768..31704359-chr6:31759116..31761149,2	MCF-7	breast:
3	chr6:31758020..31763887-chr6:31863868..31868391,6	K562	blood:
4	chr6:31758502..31767561-chr6:31786193..31804196,52	MCF-7	breast:
5	chr6:31758631..31763066-chr6:31827655..31831615,4	K562	blood:
6	chr6:31756951..31764627-chr6:31780500..31799197,32	MCF-7	breast:
7	chr6:31758779..31760923-chr6:31939769..31942169,2	K562	blood:
8	chr6:31706414..31709644-chr6:31760309..31763318,4	MCF-7	breast:
9	chr6:31759098..31761444-chr6:32081984..32084051,2	K562	blood:

No data

Variant related genes	Relation type
VARS	TF binding region
VARS	CpG island
ENSG00000204410	Chromatin interaction
ENSG00000168477	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000204344	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000204348	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000255152	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000204388	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:30 , 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	nsv884431	chr6:31732679-31761386	Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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	chr6:31745000-31762400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr6:31745200-31761000	Strong transcription	Fetal Stomach	stomach
3	chr6:31745400-31761600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:31745400-31762800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr6:31745600-31760800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:31745600-31760800	Strong transcription	HUES6 Cell Line	embryonic stem cell
7	chr6:31745600-31760800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
8	chr6:31745600-31760800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr6:31745600-31762200	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr6:31745800-31760800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
11	chr6:31745800-31760800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr6:31745800-31761000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:31745800-31762000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr6:31745800-31762000	Weak transcription	Fetal Kidney	kidney
15	chr6:31746000-31761800	Strong transcription	HUES48 Cell Line	embryonic stem cell
16	chr6:31746000-31761800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr6:31746200-31760800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr6:31746400-31761000	Strong transcription	Fetal Intestine Small	intestine
19	chr6:31750000-31762400	Weak transcription	Right Atrium	heart
20	chr6:31753200-31761800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr6:31753400-31762400	Weak transcription	Rectal Smooth Muscle	rectum
22	chr6:31753600-31761400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
23	chr6:31753600-31762000	Weak transcription	Brain Angular Gyrus	brain
24	chr6:31753800-31761800	Weak transcription	HSMMtube	muscle
25	chr6:31753800-31762000	Weak transcription	Colon Smooth Muscle	Colon
26	chr6:31754200-31762000	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr6:31756600-31760800	Strong transcription	HUES64 Cell Line	embryonic stem cell
28	chr6:31756800-31760800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr6:31757000-31760800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr6:31757000-31760800	Strong transcription	Skeletal Muscle Female	skeletal muscle
31	chr6:31757000-31761000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr6:31757000-31761000	Strong transcription	Skeletal Muscle Male	skeletal muscle
33	chr6:31757000-31761600	Strong transcription	Fetal Muscle Leg	muscle
34	chr6:31757200-31760800	Strong transcription	H9 Cell Line	embryonic stem cell
35	chr6:31757200-31760800	Genic enhancers	Primary B cells from peripheral blood	blood
36	chr6:31757200-31760800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr6:31757200-31761000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr6:31757200-31761000	Strong transcription	Placenta	Placenta
39	chr6:31757400-31762000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr6:31757400-31762000	Weak transcription	Fetal Heart	heart
41	chr6:31757400-31762000	Weak transcription	Stomach Mucosa	stomach
42	chr6:31758800-31760800	Strong transcription	Primary T cells from cord blood	blood
43	chr6:31758800-31762000	Enhancers	Primary hematopoietic stem cells	blood
44	chr6:31759000-31762000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr6:31759200-31760800	Strong transcription	Liver	Liver
46	chr6:31759200-31760800	Strong transcription	Brain Anterior Caudate	brain
47	chr6:31759200-31760800	Genic enhancers	K562	blood
48	chr6:31759200-31761000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
49	chr6:31759200-31761000	Strong transcription	Adipose Nuclei	Adipose
50	chr6:31759200-31761000	Strong transcription	Right Ventricle	heart

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