Variant report

Variant	rs409558
Chromosome Location	chr6:31708147-31708148
allele	A/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	chr6:31707671-31708467	GM12891	blood:	n/a	n/a
2	FOXM1	chr6:31707199-31708212	GM12878	blood:	n/a	n/a
3	MYC	chr6:31707388-31708260	K562	blood:	n/a	chr6:31707734-31707744
4	POLR2A	chr6:31707362-31708488	GM10847	blood:	n/a	n/a
5	POLR2A	chr6:31707561-31708416	ProgFib	skin:	n/a	n/a
6	ELF1	chr6:31707272-31708451	GM12878	blood:	n/a	n/a
7	REST	chr6:31707603-31708174	PANC-1	pancreas:	n/a	chr6:31708095-31708108 chr6:31707877-31707890
8	E2F6	chr6:31707222-31708644	H1-hESC	embryonic stem cell:	n/a	chr6:31707584-31707596 chr6:31707852-31707859 chr6:31707851-31707859 chr6:31707851-31707860 chr6:31707852-31707859 chr6:31707849-31707860 chr6:31707852-31707859 chr6:31707849-31707863 chr6:31707848-31707860 chr6:31707743-31707752 chr6:31707768-31707777
9	SIN3AK20	chr6:31707677-31708252	PANC-1	pancreas:	n/a	n/a
10	POLR2A	chr6:31705275-31708451	K562	blood:	n/a	n/a
11	USF1	chr6:31707571-31708177	ECC-1	luminal epithelium:	n/a	n/a
12	TAF7	chr6:31707633-31708430	H1-hESC	embryonic stem cell:	n/a	n/a
13	POLR2A	chr6:31707217-31708475	SK-N-MC	brain:	n/a	n/a
14	HEY1	chr6:31706843-31708524	K562	blood:	n/a	n/a
15	STAT5A	chr6:31706862-31708411	K562	blood:	n/a	chr6:31708108-31708120 chr6:31707672-31707684
16	JUND	chr6:31707288-31708202	H1-hESC	embryonic stem cell:	n/a	chr6:31707528-31707537 chr6:31707631-31707640
17	REST	chr6:31708114-31708494	SK-N-SH	brain:	n/a	n/a
18	REST	chr6:31707725-31708194	SK-N-SH	brain:	n/a	chr6:31708095-31708108 chr6:31707877-31707890
19	NFIC	chr6:31706454-31708274	GM12878	blood:	n/a	n/a
20	POLR2A	chr6:31707453-31708731	MCF-7	breast:	n/a	n/a
21	GATA3	chr6:31707074-31708247	A549	lung:	n/a	chr6:31707881-31707898 chr6:31707395-31707405
22	YY1	chr6:31707512-31708511	H1-hESC	embryonic stem cell:	n/a	chr6:31708110-31708121
23	POLR2A	chr6:31706852-31709097	PANC-1	pancreas:	n/a	n/a
24	MYC	chr6:31707362-31708289	K562	blood:	n/a	chr6:31707734-31707744
25	ZC3H11A	chr6:31707007-31708304	K562	blood:	n/a	n/a
26	YY1	chr6:31707617-31708415	H1-hESC	embryonic stem cell:	n/a	chr6:31708110-31708121
27	SIN3AK20	chr6:31707289-31708448	K562	blood:	n/a	n/a
28	TAF1	chr6:31707239-31708491	K562	blood:	n/a	n/a
29	ZMIZ1	chr6:31705309-31708339	K562	blood:	n/a	n/a
30	MAX	chr6:31707126-31708370	SK-N-SH	brain:	n/a	chr6:31707734-31707744
31	POLR2A	chr6:31707339-31708433	GM12892	blood:	n/a	n/a
32	ZNF143	chr6:31708070-31708155	Hela-S3	cervix:	n/a	n/a
33	BHLHE40	chr6:31707254-31708193	GM12878	blood:	n/a	n/a
34	MBD4	chr6:31705115-31708186	HepG2	liver:	n/a	n/a
35	POLR2A	chr6:31707155-31708615	HUVEC	blood vessel:	n/a	n/a
36	POLR2A	chr6:31707331-31708517	ECC-1	luminal epithelium:	n/a	n/a
37	SP1	chr6:31707150-31708235	HCT-116	colon:	n/a	chr6:31707734-31707744 chr6:31707734-31707743 chr6:31707730-31707744 chr6:31707735-31707744 chr6:31707733-31707745 chr6:31707580-31707594 chr6:31707609-31707618 chr6:31707733-31707745 chr6:31707628-31707649 chr6:31708099-31708109
38	TEAD4	chr6:31705115-31708474	K562	blood:	n/a	n/a
39	MYC	chr6:31707063-31708612	NB4	blood:	n/a	chr6:31707734-31707744
40	RELA	chr6:31705616-31708216	GM19193	blood:	n/a	n/a
41	USF2	chr6:31707564-31708265	K562	blood:	n/a	n/a
42	YY1	chr6:31707296-31708682	GM12878	blood:	n/a	chr6:31708110-31708121
43	MAZ	chr6:31705267-31708428	K562	blood:	n/a	chr6:31705423-31705432 chr6:31707734-31707744
44	CHD2	chr6:31707325-31708327	H1-hESC	embryonic stem cell:	n/a	n/a
45	USF2	chr6:31707610-31708154	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr6:31707286-31708408	HCT-116	colon:	n/a	n/a
47	REST	chr6:31707617-31708555	PFSK-1	brain:	n/a	chr6:31708095-31708108 chr6:31707877-31707890
48	POLR2A	chr6:31707013-31708479	GM18526	blood:	n/a	n/a
49	SP1	chr6:31705167-31708177	A549	lung:	n/a	chr6:31706876-31706885 chr6:31707734-31707744 chr6:31707734-31707743 chr6:31707730-31707744 chr6:31707735-31707744 chr6:31706098-31706107 chr6:31707733-31707745 chr6:31705835-31705848 chr6:31705486-31705496 chr6:31707580-31707594 chr6:31707609-31707618 chr6:31705486-31705495 chr6:31706875-31706885 chr6:31707733-31707745 chr6:31707628-31707649 chr6:31706755-31706769 chr6:31708099-31708109
50	JUND	chr6:31705274-31708376	K562	blood:	n/a	chr6:31707528-31707537 chr6:31707631-31707640

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31708121-31708171	HRCEpiC	kidney:	n/a
2	chr6:31708121-31708171	GM12878	blood:	n/a
3	chr6:31708121-31708171	HCPEpiC	choroid plexus:	n/a
4	chr6:31708121-31708171	AG09319	gingival:	n/a
5	chr6:31708121-31708171	HCM	heart:	n/a
6	chr6:31708121-31708171	HUVEC	blood vessel:	n/a
7	chr6:31708121-31708171	GM06990	blood:	n/a
8	chr6:31708121-31708171	Jurkat	blood:	n/a
9	chr6:31708121-31708171	HIPEpiC	eye:	n/a
10	chr6:31708121-31708171	HL-60	blood:	n/a
11	chr6:31708121-31708171	H1-hESC	embryonic stem cell:	embryo
12	chr6:31708121-31708171	SK-N-SH_RA	brain:	n/a
13	chr6:31708121-31708171	MCF-7	breast:	n/a
14	chr6:31708121-31708171	NB4	blood:	n/a
15	chr6:31708121-31708171	AG04449	skin:	fetal
16	chr6:31708121-31708171	HEEpiC	esophagus:	n/a
17	chr6:31708121-31708171	AG10803	skin:	n/a
18	chr6:31708121-31708171	SK-N-MC	brain:	n/a
19	chr6:31708121-31708171	Hela-S3	cervix:	n/a
20	chr6:31708121-31708171	HNPCEpiC	eye:	n/a
21	chr6:31708121-31708171	NHDF-neo	bronchial:	n/a
22	chr6:31708121-31708171	U87	brain:	n/a
23	chr6:31708121-31708171	AoSMC	blood vessel:	n/a
24	chr6:31708121-31708171	ECC-1	luminal epithelium:	n/a
25	chr6:31708121-31708171	Hepatocyte	liver:	n/a
26	chr6:31708121-31708171	PANC-1	pancreas:	n/a
27	chr6:31708121-31708171	ovcar-3	ovarian:	n/a
28	chr6:31708121-31708171	LNCaP	prostate:	n/a
29	chr6:31708121-31708171	IMR90	lung:	fetal
30	chr6:31708121-31708171	AG09309	skin:	n/a
31	chr6:31708121-31708171	MCF10A-Er-Src	breast:	n/a
32	chr6:31708121-31708171	BE2_C	brain:	n/a
33	chr6:31708121-31708171	HEK293	kidney:	embryo
34	chr6:31708121-31708171	PrEC	prostate:	n/a
35	chr6:31708121-31708171	GM12891	blood:	n/a
36	chr6:31708121-31708171	NHBE	bronchial:	n/a
37	chr6:31708121-31708171	ProgFib	skin:	n/a
38	chr6:31708121-31708171	HCF	heart:	n/a
39	chr6:31708121-31708171	HRPEpiC	eye:	n/a
40	chr6:31708121-31708171	Caco-2	colon:	n/a
41	chr6:31708121-31708171	SK-N-SH	brain:	n/a
42	chr6:31708121-31708171	K562	blood:	n/a
43	chr6:31708121-31708171	NT2-D1	testis:	n/a
44	chr6:31708121-31708171	HCT-116	colon:	n/a
45	chr6:31708121-31708171	T-47D	breast:	n/a
46	chr6:31708121-31708171	HAEpiC	amniotic membrane:	n/a
47	chr6:31708121-31708171	HRE	kidney:	n/a
48	chr6:31708121-31708171	HPAEpiC	pulmonary alveolar:	n/a
49	chr6:31708121-31708171	CMK	blood:	n/a
50	chr6:31708121-31708171	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:31706534..31708652-chr6:31828813..31831366,2	K562	blood:
2	chr6:31707439..31709705-chr6:31719652..31722031,2	MCF-7	breast:
3	chr6:31706755..31708433-chr6:31830637..31832576,2	K562	blood:
4	chr6:31620775..31623476-chr6:31707593..31710385,2	MCF-7	breast:
5	chr6:31632318..31634134-chr6:31707864..31709911,2	MCF-7	breast:
6	chr6:31705956..31708779-chr6:32940419..32942234,2	K562	blood:
7	chr6:31706414..31709644-chr6:31760309..31763318,4	MCF-7	breast:
8	chr6:31706404..31710413-chr6:31739544..31742193,3	MCF-7	breast:
9	chr6:31619534..31622102-chr6:31706429..31708950,2	MCF-7	breast:
10	chr6:31705740..31708202-chr6:31937563..31940759,3	K562	blood:
11	chr6:31706953..31708752-chr6:31729698..31731457,2	MCF-7	breast:
12	chr6:31707530..31710458-chr6:31763602..31765832,2	MCF-7	breast:
13	chr6:31513816..31516540-chr6:31705988..31708603,3	K562	blood:
14	chr6:31646441..31651407-chr6:31704606..31708985,8	MCF-7	breast:
15	chr6:31656167..31662607-chr6:31701760..31709122,7	MCF-7	breast:
16	chr6:31706634..31708801-chr6:31800658..31802483,2	MCF-7	breast:
17	chr6:31706679..31708956-chr6:31795250..31798080,2	MCF-7	breast:
18	chr6:31707816..31708338-chr9:88968948..88969697,2	NB4	blood:
19	chr6:31706580..31708960-chr6:31728802..31732177,3	MCF-7	breast:
20	chr6:31705460..31708202-chr6:31937853..31939865,2	K562	blood:
21	chr6:31632814..31634832-chr6:31706820..31709460,2	MCF-7	breast:
22	chr6:31707659..31709332-chr6:31732393..31734273,2	MCF-7	breast:

Variant related genes	Relation type
MSH5	TF binding region
CLIC1	TF binding region
CLIC1	CpG island
MSH5	CpG island
ENSG00000213760	Chromatin interaction
ENSG00000204256	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000204427	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000204344	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000204498	Chromatin interaction
ENSG00000235663	Chromatin interaction
ENSG00000254870	Chromatin interaction
ENSG00000255152	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000204394	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000083223	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000204396	Chromatin interaction
ENSG00000263756	Chromatin interaction
ENSG00000204348	Chromatin interaction
ENSG00000228727	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000204428	Chromatin interaction
ENSG00000204410	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs2075788	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2075801	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2293861	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3130486	0.95[ASN][1000 genomes]
rs3749953	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3828922	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6905572	0.81[EUR][1000 genomes]
rs9469051	0.82[AFR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 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	nsv432868	chr6:31338844-31721033	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer 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	250 gene(s)	inside rSNPs	diseases
10	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
11	nsv884418	chr6:31525448-31741078	Active TSS Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	206 gene(s)	inside rSNPs	diseases
12	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
13	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
14	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

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs409558	DOM3Z	Cis_1M	lymphoblastoid	RTeQTL
rs409558	FKBP5	cis	cerebellum	SCAN
rs409558	TBX10	trans	cerebellum	SCAN

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31702400-31708800	Flanking Active TSS	Primary hematopoietic stem cells	blood
2	chr6:31704200-31709000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr6:31704200-31709000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr6:31704400-31708800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
5	chr6:31704400-31709000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
6	chr6:31706600-31708800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr6:31706600-31708800	Active TSS	A549	lung
8	chr6:31706800-31708800	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr6:31707000-31708400	Flanking Active TSS	Liver	Liver
10	chr6:31707000-31708400	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr6:31707000-31708400	Active TSS	HSMMtube	muscle
12	chr6:31707000-31709000	Enhancers	Fetal Brain Male	brain
13	chr6:31707000-31709200	Active TSS	Brain Germinal Matrix	brain
14	chr6:31707200-31708200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
15	chr6:31707200-31708200	Active TSS	Pancreas	Pancrea
16	chr6:31707200-31708400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr6:31707200-31708400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr6:31707200-31708400	Active TSS	Fetal Kidney	kidney
19	chr6:31707200-31708400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
20	chr6:31707200-31708600	Active TSS	H9 Cell Line	embryonic stem cell
21	chr6:31707200-31708600	Active TSS	HUES6 Cell Line	embryonic stem cell
22	chr6:31707200-31708600	Flanking Active TSS	Adipose Nuclei	Adipose
23	chr6:31707200-31708800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr6:31707200-31708800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
25	chr6:31707200-31708800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
26	chr6:31707200-31708800	Flanking Active TSS	Fetal Muscle Leg	muscle
27	chr6:31707200-31709000	Flanking Active TSS	Primary B cells from cord blood	blood
28	chr6:31707400-31708200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr6:31707400-31708200	Active TSS	Muscle Satellite Cultured Cells	--
30	chr6:31707400-31708200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr6:31707400-31708200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr6:31707400-31708200	Active TSS	Fetal Lung	lung
33	chr6:31707400-31708200	Active TSS	HMEC	breast
34	chr6:31707400-31708400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr6:31707400-31708400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr6:31707400-31708400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr6:31707400-31708400	Active TSS	Brain Angular Gyrus	brain
38	chr6:31707400-31708400	Active TSS	Brain Inferior Temporal Lobe	brain
39	chr6:31707400-31708400	Active TSS	Ovary	ovary
40	chr6:31707400-31708400	Active TSS	Stomach Mucosa	stomach
41	chr6:31707400-31708600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr6:31707400-31708600	Active TSS	iPS-18 Cell Line	embryonic stem cell
43	chr6:31707400-31708600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr6:31707400-31708600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr6:31707400-31708600	Active TSS	Breast Myoepithelial Primary Cells	Breast
46	chr6:31707400-31708600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr6:31707400-31708600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr6:31707400-31708600	Active TSS	Brain Anterior Caudate	brain
49	chr6:31707400-31708600	Active TSS	Brain Hippocampus Middle	brain
50	chr6:31707400-31708600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain

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