Variant report

Variant	rs34431565
Chromosome Location	chr6:31782180-31782181
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:41)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:41 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:31781895-31782245	Hela-S3	cervix:	n/a	n/a
2	HCFC1	chr6:31781524-31783637	Hela-S3	cervix:	n/a	n/a
3	RAD21	chr6:31782049-31782225	K562	blood:	n/a	n/a
4	REST	chr6:31782010-31782237	K562	blood:	n/a	n/a
5	POLR2A	chr6:31782003-31782237	K562	blood:	n/a	n/a
6	POLR2A	chr6:31781793-31782292	Hela-S3	cervix:	n/a	n/a
7	POLR2A	chr6:31781969-31783588	K562	blood:	n/a	n/a
8	YY1	chr6:31781940-31782213	K562	blood:	n/a	n/a
9	E2F6	chr6:31782025-31782222	K562	blood:	n/a	n/a
10	POLR2A	chr6:31781954-31782234	ProgFib	skin:	n/a	n/a
11	MAX	chr6:31782052-31783542	K562	blood:	n/a	chr6:31783047-31783056 chr6:31782900-31782910 chr6:31783079-31783089
12	UBTF	chr6:31781626-31782785	K562	blood:	n/a	n/a
13	EP300	chr6:31781201-31783632	SK-N-SH	brain:	n/a	chr6:31782928-31782944 chr6:31782372-31782385 chr6:31782453-31782466
14	CBX3	chr6:31781275-31785537	K562	blood:	n/a	n/a
15	POLR2A	chr6:31781587-31785535	Hela-S3	cervix:	n/a	n/a
16	UBTF	chr6:31781679-31783686	K562	blood:	n/a	n/a
17	POLR2A	chr6:31781958-31783691	Hela-S3	cervix:	n/a	n/a
18	STAT3	chr6:31782167-31782793	MCF10A-Er-Src	breast:	n/a	chr6:31782467-31782479 chr6:31782777-31782789 chr6:31782457-31782469
19	TAF1	chr6:31781760-31782250	K562	blood:	n/a	n/a
20	REST	chr6:31782043-31782223	K562	blood:	n/a	n/a
21	STAT3	chr6:31782154-31783481	MCF10A-Er-Src	breast:	n/a	chr6:31782467-31782479 chr6:31782777-31782789 chr6:31782457-31782469
22	POLR2A	chr6:31781939-31787367	K562	blood:	n/a	n/a
23	MAX	chr6:31781632-31783598	K562	blood:	n/a	chr6:31783047-31783056 chr6:31782900-31782910 chr6:31783079-31783089
24	POLR2A	chr6:31782025-31784136	HUVEC	blood vessel:	n/a	n/a
25	NR2F2	chr6:31781154-31786921	K562	blood:	n/a	n/a
26	MYC	chr6:31782132-31783585	K562	blood:	n/a	chr6:31783047-31783056 chr6:31782900-31782910 chr6:31783079-31783089
27	PAX5	chr6:31782027-31782302	GM12878	blood:	n/a	n/a
28	POLR2A	chr6:31782107-31783937	PANC-1	pancreas:	n/a	n/a
29	POLR2A	chr6:31782154-31782288	MCF-7	breast:	n/a	n/a
30	TEAD4	chr6:31781225-31783609	K562	blood:	n/a	n/a
31	HEY1	chr6:31781950-31782259	K562	blood:	n/a	n/a
32	POLR2A	chr6:31781409-31782241	K562	blood:	n/a	n/a
33	YY1	chr6:31781960-31782290	K562	blood:	n/a	n/a
34	YY1	chr6:31782014-31782678	HepG2	liver:	n/a	chr6:31782506-31782518 chr6:31782507-31782529
35	POLR2A	chr6:31782044-31782224	A549	lung:	n/a	n/a
36	POLR2A	chr6:31782013-31782252	A549	lung:	n/a	n/a
37	MAZ	chr6:31782177-31783625	IMR90	lung:	n/a	chr6:31783047-31783056 chr6:31782900-31782910 chr6:31783079-31783089
38	POLR2A	chr6:31781957-31782250	ECC-1	luminal epithelium:	n/a	n/a
39	POLR2A	chr6:31782091-31785254	HepG2	liver:	n/a	n/a
40	POLR2A	chr6:31782129-31783586	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr6:31782124-31783597	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31782158-31782208	PANC-1	pancreas:	n/a
2	chr6:31782158-31782208	IMR90	lung:	fetal
3	chr6:31782158-31782208	HEEpiC	esophagus:	n/a
4	chr6:31782158-31782208	U87	brain:	n/a
5	chr6:31782158-31782208	NHBE	bronchial:	n/a
6	chr6:31782158-31782208	T-47D	breast:	n/a
7	chr6:31782158-31782208	PFSK-1	brain:	n/a
8	chr6:31782158-31782208	AG04450	lung:	fetal
9	chr6:31782158-31782208	HPAEpiC	pulmonary alveolar:	n/a
10	chr6:31782158-31782208	SKMC	muscle:	n/a
11	chr6:31782158-31782208	MCF-7	breast:	n/a
12	chr6:31782158-31782208	A549	lung:	n/a
13	chr6:31782158-31782208	GM12891	blood:	n/a
14	chr6:31782158-31782208	ProgFib	skin:	n/a
15	chr6:31782158-31782208	GM06990	blood:	n/a
16	chr6:31782158-31782208	AG09309	skin:	n/a
17	chr6:31782158-31782208	HIPEpiC	eye:	n/a
18	chr6:31782158-31782208	Hepatocyte	liver:	n/a
19	chr6:31782158-31782208	HCM	heart:	n/a
20	chr6:31782158-31782208	SK-N-MC	brain:	n/a
21	chr6:31782158-31782208	CMK	blood:	n/a
22	chr6:31782158-31782208	K562	blood:	n/a
23	chr6:31782158-31782208	AG10803	skin:	n/a
24	chr6:31782158-31782208	ECC-1	luminal epithelium:	n/a
25	chr6:31782158-31782208	GM12878	blood:	n/a
26	chr6:31782158-31782208	H1-hESC	embryonic stem cell:	embryo
27	chr6:31782158-31782208	SK-N-SH_RA	brain:	n/a
28	chr6:31782158-31782208	Hela-S3	cervix:	n/a
29	chr6:31782158-31782208	BE2_C	brain:	n/a
30	chr6:31782158-31782208	NT2-D1	testis:	n/a
31	chr6:31782158-31782208	NH-A	brain:	n/a
32	chr6:31782158-31782208	GM19239	blood:	n/a
33	chr6:31782158-31782208	AG04449	skin:	fetal
34	chr6:31782158-31782208	HCPEpiC	choroid plexus:	n/a
35	chr6:31782158-31782208	SAEC	small airway:	n/a
36	chr6:31782158-31782208	HL-60	blood:	n/a
37	chr6:31782158-31782208	HEK293	kidney:	embryo
38	chr6:31782158-31782208	GM12892	blood:	n/a
39	chr6:31782158-31782208	HNPCEpiC	eye:	n/a
40	chr6:31782158-31782208	RPTEC	kidney:	n/a
41	chr6:31782158-31782208	HepG2	liver:	n/a
42	chr6:31782158-31782208	HRCEpiC	kidney:	n/a
43	chr6:31782158-31782208	SK-N-SH	brain:	n/a
44	chr6:31782158-31782208	AG09319	gingival:	n/a
45	chr6:31782158-31782208	AoSMC	blood vessel:	n/a
46	chr6:31782158-31782208	NB4	blood:	n/a
47	chr6:31782158-31782208	HRE	kidney:	n/a
48	chr6:31782158-31782208	HMEC	breast:	n/a
49	chr6:31782158-31782208	HCF	heart:	n/a
50	chr6:31782158-31782208	Jurkat	blood:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31781796..31783894-chr6:31925428..31927086,2	K562	blood:
2	chr6:31781417..31783934-chr6:32937499..32939420,2	K562	blood:
3	chr6:31780821..31784746-chr6:31829825..31831701,4	MCF-7	breast:
4	chr6:31507867..31510784-chr6:31781026..31784406,3	MCF-7	breast:
5	chr6:31782095..31783822-chr6:31794892..31795963,5	MCF-7	breast:
6	chr6:31782025..31784864-chr6:32163977..32165547,2	K562	blood:
7	chr6:31781780..31785433-chr6:31828310..31832689,5	K562	blood:
8	chr6:31780396..31783150-chr6:32157710..32160077,2	K562	blood:
9	chr6:31781780..31785433-chr6:31829263..31832689,6	K562	blood:
10	chr6:31743107..31747994-chr6:31781956..31785553,7	MCF-7	breast:
11	chr6:31780956..31783456-chr6:31865283..31866829,2	K562	blood:
12	chr6:31780296..31786175-chr6:31828333..31833086,7	MCF-7	breast:
13	chr6:31759482..31765185-chr6:31781824..31784897,13	MCF-7	breast:
14	chr6:31756951..31764627-chr6:31780500..31799197,32	MCF-7	breast:
15	chr6:31508732..31511014-chr6:31781931..31784408,2	K562	blood:
16	chr6:31781258..31784668-chr6:32935964..32938963,3	MCF-7	breast:
17	chr6:31781426..31784987-chr6:31937458..31940746,3	K562	blood:
18	chr6:31780574..31784383-chr6:31865157..31867218,4	K562	blood:

No data

Variant related genes	Relation type
HSPA1A	TF binding region
HSPA1A	CpG island
ENSG00000265236	Chromatin interaction
ENSG00000204394	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000223837	Chromatin interaction
ENSG00000234006	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000204348	Chromatin interaction
ENSG00000204396	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000204257	Chromatin interaction
ENSG00000204304	Chromatin interaction
ENSG00000204356	Chromatin interaction
ENSG00000204351	Chromatin interaction
ENSG00000204256	Chromatin interaction
ENSG00000204344	Chromatin interaction
ENSG00000201555	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000204301	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1062309	0.85[AMR][1000 genomes]
rs17200969	0.85[AMR][1000 genomes]
rs28745897	0.87[AMR][1000 genomes]
rs62395791	0.85[AMR][1000 genomes]
rs62395804	0.85[AMR][1000 genomes]
rs62395814	0.85[AMR][1000 genomes]
rs62395823	0.85[AMR][1000 genomes]
rs62395827	1.00[ASN][1000 genomes]
rs62395828	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62395833	0.83[EUR][1000 genomes]
rs62395851	0.92[ASN][1000 genomes]
rs6907185	0.92[ASN][1000 genomes]
rs7769158	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 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	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
19	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
20	nsv981359	chr6:31779004-31797103	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	111 gene(s)	inside rSNPs	diseases
21	nsv869989	chr6:31779203-31797657	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	114 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31774800-31782600	Weak transcription	Lung	lung
2	chr6:31774800-31783000	Weak transcription	Gastric	stomach
3	chr6:31780200-31782200	Enhancers	Primary T helper naive cells from peripheral blood	blood
4	chr6:31780600-31782200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
5	chr6:31780800-31782200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
6	chr6:31780800-31782400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr6:31781000-31782400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
8	chr6:31781000-31782400	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr6:31781000-31782400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
10	chr6:31781200-31782200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr6:31781400-31782200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr6:31781400-31783400	Flanking Active TSS	Primary B cells from cord blood	blood
13	chr6:31781600-31782200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
14	chr6:31781600-31782200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
15	chr6:31781600-31782200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr6:31781600-31782200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
17	chr6:31781600-31782200	Flanking Active TSS	Fetal Intestine Small	intestine
18	chr6:31781600-31782200	Flanking Active TSS	Fetal Muscle Trunk	muscle
19	chr6:31781600-31782200	Flanking Active TSS	Fetal Muscle Leg	muscle
20	chr6:31781600-31782200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
21	chr6:31781600-31782200	Flanking Active TSS	Thymus	Thymus
22	chr6:31781600-31782800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
23	chr6:31781600-31782800	Active TSS	Right Atrium	heart
24	chr6:31781600-31783000	Active TSS	Colonic Mucosa	Colon
25	chr6:31781600-31783600	Active TSS	ES-I3 Cell Line	embryonic stem cell
26	chr6:31781600-31783600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
27	chr6:31781600-31783800	Active TSS	H9 Cell Line	embryonic stem cell
28	chr6:31781600-31783800	Active TSS	HUES64 Cell Line	embryonic stem cell
29	chr6:31781600-31783800	Active TSS	Fetal Brain Female	brain
30	chr6:31781600-31783800	Active TSS	Left Ventricle	heart
31	chr6:31781600-31783800	Active TSS	Right Ventricle	heart
32	chr6:31781800-31782200	Flanking Active TSS	Primary B cells from peripheral blood	blood
33	chr6:31781800-31782200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
34	chr6:31781800-31782200	Flanking Active TSS	Fetal Intestine Large	intestine
35	chr6:31781800-31782200	Flanking Active TSS	Placenta	Placenta
36	chr6:31781800-31782200	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
37	chr6:31781800-31782600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr6:31781800-31782600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr6:31781800-31782600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr6:31781800-31782600	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
41	chr6:31781800-31782600	Weak transcription	Aorta	Aorta
42	chr6:31781800-31783600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr6:31781800-31783600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr6:31781800-31783600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
45	chr6:31781800-31783600	Active TSS	Brain Angular Gyrus	brain
46	chr6:31781800-31783600	Active TSS	Brain Substantia Nigra	brain
47	chr6:31781800-31783600	Active TSS	Duodenum Smooth Muscle	Duodenum
48	chr6:31781800-31783600	Active TSS	Ovary	ovary
49	chr6:31781800-31783600	Active TSS	NHLF	lung
50	chr6:31781800-31783800	Active TSS	H1 Cell Line	embryonic stem cell

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