Variant report

Variant	rs2961674
Chromosome Location	chr5:177632527-177632528
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	MYC	chr5:177630868-177632684	K562	blood:	n/a	n/a
2	POLR2A	chr5:177630918-177635502	HepG2	liver:	n/a	n/a
3	POLR2A	chr5:177632232-177633236	GM12891	blood:	n/a	n/a
4	RCOR1	chr5:177632401-177633361	K562	blood:	n/a	n/a
5	POLR2A	chr5:177630947-177632842	GM19193	blood:	n/a	n/a
6	STAT1	chr5:177632397-177632645	GM12878	blood:	n/a	chr5:177632429-177632441
7	POLR2A	chr5:177632210-177635513	PANC-1	pancreas:	n/a	n/a
8	POLR2A	chr5:177630886-177634610	HL-60	blood:	n/a	n/a
9	TBL1XR1	chr5:177632205-177633547	K562	blood:	n/a	n/a
10	EGR1	chr5:177631949-177632548	GM12878	blood:	n/a	chr5:177632384-177632397 chr5:177632386-177632396 chr5:177632385-177632396 chr5:177632384-177632397 chr5:177632385-177632396 chr5:177632384-177632397 chr5:177632384-177632397 chr5:177632386-177632396 chr5:177632383-177632398 chr5:177632384-177632398 chr5:177632386-177632395 chr5:177632380-177632402 chr5:177632387-177632396
11	POLR2A	chr5:177631885-177632779	K562	blood:	n/a	n/a
12	ATF2	chr5:177632330-177633205	H1-hESC	embryonic stem cell:	n/a	n/a
13	POLR2A	chr5:177630891-177643467	GM18505	blood:	n/a	n/a
14	PAX5	chr5:177631928-177632565	GM12892	blood:	n/a	n/a
15	PML	chr5:177632210-177632865	MCF-7	breast:	n/a	n/a
16	EGR1	chr5:177632041-177632920	HCT-116	colon:	n/a	chr5:177632384-177632397 chr5:177632386-177632396 chr5:177632385-177632396 chr5:177632384-177632397 chr5:177632385-177632396 chr5:177632384-177632397 chr5:177632384-177632397 chr5:177632386-177632396 chr5:177632383-177632398 chr5:177632384-177632398 chr5:177632386-177632395 chr5:177632380-177632402 chr5:177632387-177632396
17	YY1	chr5:177631084-177632630	HepG2	liver:	n/a	chr5:177631589-177631598 chr5:177631291-177631300 chr5:177632371-177632385 chr5:177631749-177631760
18	EGR1	chr5:177631927-177632577	K562	blood:	n/a	chr5:177632384-177632397 chr5:177632386-177632396 chr5:177632385-177632396 chr5:177632384-177632397 chr5:177632385-177632396 chr5:177632384-177632397 chr5:177632384-177632397 chr5:177632386-177632396 chr5:177632383-177632398 chr5:177632384-177632398 chr5:177632386-177632395 chr5:177632380-177632402 chr5:177632387-177632396
19	SIN3AK20	chr5:177632327-177632585	K562	blood:	n/a	n/a
20	PAX5	chr5:177632155-177632784	GM12878	blood:	n/a	n/a
21	ELK1	chr5:177632397-177634092	K562	blood:	n/a	n/a
22	POLR2A	chr5:177631061-177632748	H1-neurons	neurons:	n/a	n/a
23	POLR2A	chr5:177630906-177632717	GM18951	blood:	n/a	n/a
24	MAX	chr5:177631098-177632563	K562	blood:	n/a	n/a
25	POLR2A	chr5:177631022-177632651	GM10847	blood:	n/a	n/a
26	MAX	chr5:177630995-177632651	HepG2	liver:	n/a	n/a
27	ELF1	chr5:177632162-177632532	HepG2	liver:	n/a	chr5:177632356-177632365 chr5:177632350-177632362
28	POLR2A	chr5:177630884-177632853	GM12878	blood:	n/a	n/a
29	CHD2	chr5:177631070-177633577	K562	blood:	n/a	chr5:177632401-177632411 chr5:177631641-177631651 chr5:177631771-177631781
30	ZC3H11A	chr5:177632229-177633271	K562	blood:	n/a	n/a
31	POLR2A	chr5:177630831-177644633	GM12892	blood:	n/a	n/a
32	RUNX3	chr5:177632320-177632675	GM12878	blood:	n/a	n/a
33	MAX	chr5:177632239-177632550	K562	blood:	n/a	n/a
34	MAZ	chr5:177630949-177632702	Hela-S3	cervix:	n/a	n/a
35	EGR1	chr5:177632191-177632707	ECC-1	luminal epithelium:	n/a	chr5:177632384-177632397 chr5:177632386-177632396 chr5:177632385-177632396 chr5:177632384-177632397 chr5:177632385-177632396 chr5:177632384-177632397 chr5:177632384-177632397 chr5:177632386-177632396 chr5:177632383-177632398 chr5:177632384-177632398 chr5:177632386-177632395 chr5:177632380-177632402 chr5:177632387-177632396
36	E2F4	chr5:177632237-177632649	GM12878	blood:	n/a	chr5:177632399-177632414 chr5:177632373-177632382 chr5:177632378-177632388
37	POLR2A	chr5:177630957-177632909	GM12892	blood:	n/a	n/a
38	MXI1	chr5:177630790-177633795	IMR90	lung:	n/a	n/a
39	BACH1	chr5:177632149-177632720	H1-hESC	embryonic stem cell:	n/a	n/a
40	TCF7L2	chr5:177631073-177632708	PANC-1	pancreas:	n/a	n/a
41	RCOR1	chr5:177631991-177633098	K562	blood:	n/a	n/a
42	POLR2A	chr5:177630864-177635435	HL-60	blood:	n/a	n/a
43	MYC	chr5:177631025-177632645	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr5:177630805-177644118	GM12878	blood:	n/a	n/a
45	ELF1	chr5:177630841-177632640	GM12878	blood:	n/a	chr5:177631489-177631501 chr5:177631746-177631758 chr5:177632356-177632365 chr5:177632350-177632362
46	SIN3AK20	chr5:177632374-177632687	A549	lung:	n/a	n/a
47	MTA3	chr5:177632275-177633820	GM12878	blood:	n/a	n/a
48	TAF7	chr5:177630817-177632813	H1-hESC	embryonic stem cell:	n/a	n/a
49	ZNF263	chr5:177632161-177637723	HEK293-T-REx	kidney:	n/a	n/a
50	POLR2A	chr5:177631094-177644651	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:177632507-177632557	BE2_C	brain:	n/a
2	chr5:177632507-177632557	MCF10A-Er-Src	breast:	n/a
3	chr5:177632507-177632557	GM12892	blood:	n/a
4	chr5:177632507-177632557	LNCaP	prostate:	n/a
5	chr5:177632507-177632557	U87	brain:	n/a
6	chr5:177632507-177632557	GM19239	blood:	n/a
7	chr5:177632507-177632557	AG04450	lung:	fetal
8	chr5:177632507-177632557	T-47D	breast:	n/a
9	chr5:177632507-177632557	HPAEpiC	pulmonary alveolar:	n/a
10	chr5:177632507-177632557	HEK293	kidney:	embryo
11	chr5:177632507-177632557	HRCEpiC	kidney:	n/a
12	chr5:177632507-177632557	HNPCEpiC	eye:	n/a
13	chr5:177632507-177632557	NT2-D1	testis:	n/a
14	chr5:177632507-177632557	PANC-1	pancreas:	n/a
15	chr5:177632507-177632557	GM12878	blood:	n/a
16	chr5:177632507-177632557	BJ	skin:	n/a
17	chr5:177632507-177632557	PrEC	prostate:	n/a
18	chr5:177632507-177632557	ECC-1	luminal epithelium:	n/a
19	chr5:177632507-177632557	NHDF-neo	bronchial:	n/a
20	chr5:177632507-177632557	Hepatocyte	liver:	n/a
21	chr5:177632507-177632557	HUVEC	blood vessel:	n/a
22	chr5:177632507-177632557	HIPEpiC	eye:	n/a
23	chr5:177632507-177632557	SK-N-SH	brain:	n/a
24	chr5:177632507-177632557	AG04449	skin:	fetal
25	chr5:177632507-177632557	HEEpiC	esophagus:	n/a
26	chr5:177632507-177632557	HCPEpiC	choroid plexus:	n/a
27	chr5:177632507-177632557	HRPEpiC	eye:	n/a
28	chr5:177632507-177632557	AG10803	skin:	n/a
29	chr5:177632507-177632557	AoSMC	blood vessel:	n/a
30	chr5:177632507-177632557	GM06990	blood:	n/a
31	chr5:177632507-177632557	SAEC	small airway:	n/a
32	chr5:177632507-177632557	CMK	blood:	n/a
33	chr5:177632507-177632557	Jurkat	blood:	n/a
34	chr5:177632507-177632557	HAEpiC	amniotic membrane:	n/a
35	chr5:177632507-177632557	PFSK-1	brain:	n/a
36	chr5:177632507-177632557	HRE	kidney:	n/a
37	chr5:177632507-177632557	MCF-7	breast:	n/a
38	chr5:177632507-177632557	NH-A	brain:	n/a
39	chr5:177632507-177632557	RPTEC	kidney:	n/a
40	chr5:177632507-177632557	K562	blood:	n/a
41	chr5:177632507-177632557	SK-N-MC	brain:	n/a
42	chr5:177632507-177632557	Caco-2	colon:	n/a
43	chr5:177632507-177632557	SK-N-SH_RA	brain:	n/a
44	chr5:177632507-177632557	NHBE	bronchial:	n/a
45	chr5:177632507-177632557	Hela-S3	cervix:	n/a
46	chr5:177632507-177632557	HepG2	liver:	n/a
47	chr5:177632507-177632557	IMR90	lung:	fetal
48	chr5:177632507-177632557	HMEC	breast:	n/a
49	chr5:177632507-177632557	AG09309	skin:	n/a
50	chr5:177632507-177632557	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:3982997..3985280-chr5:177631558..177634299,2	K562	blood:
2	chr5:177556499..177561085-chr5:177629309..177633856,7	K562	blood:
3	chr5:176792166..176794186-chr5:177632419..177635026,2	K562	blood:
4	chr5:176942187..176944181-chr5:177630972..177633765,3	K562	blood:
5	chr5:177025539..177028252-chr5:177630597..177632555,2	K562	blood:
6	chr5:177588875..177592834-chr5:177630545..177633533,4	K562	blood:
7	chr5:177632239..177635165-chr5:179247019..179248858,2	K562	blood:
8	chr5:177578534..177581104-chr5:177631476..177634038,2	MCF-7	breast:
9	chr5:177017384..177019488-chr5:177631001..177633000,2	MCF-7	breast:
10	chr5:177630812..177632588-chr6:26155741..26158139,2	MCF-7	breast:
11	chr16:22018965..22019590-chr5:177631826..177632604,2	Hela-S3	cervix:
12	chr5:177631162..177632942-chr5:178051796..178054079,4	K562	blood:
13	chr2:88927008..88927587-chr5:177631246..177632535,3	Hela-S3	cervix:
14	chr5:177591354..177594975-chr5:177630282..177634044,5	MCF-7	breast:
15	chr5:177631253..177632828-chr5:178016105..178018488,2	MCF-7	breast:
16	chr5:177630932..177632998-chr5:178042770..178045637,2	K562	blood:
17	chr5:177572705..177577722-chr5:177630592..177633512,5	MCF-7	breast:
18	chr17:59477135..59479003-chr5:177630296..177633273,2	MCF-7	breast:
19	chr5:177578478..177582579-chr5:177629428..177633237,12	MCF-7	breast:
20	chr5:177631376..177633067-chr5:178051942..178054079,2	K562	blood:
21	chr5:177579578..177582486-chr5:177629664..177632966,4	K562	blood:
22	chr18:13542130..13544313-chr5:177631134..177632861,2	MCF-7	breast:
23	chr5:177631720..177633728-chr6:25726576..25729132,2	K562	blood:
24	chr5:177631876..177633528-chr5:179047045..179049302,2	MCF-7	breast:
25	chr5:41924876..41925465-chr5:177631659..177632543,2	Hela-S3	cervix:
26	chr5:177555803..177560183-chr5:177628551..177633825,8	MCF-7	breast:
27	chr5:177568592..177570567-chr5:177631471..177633175,2	MCF-7	breast:
28	chr5:177538337..177541901-chr5:177630904..177633261,3	K562	blood:
29	chr5:177556514..177559685-chr5:177630098..177633052,4	K562	blood:

Variant related genes	Relation type
HNRNPAB	TF binding region
HNRNPAB	CpG island
ENSG00000027847	Chromatin interaction
ENSG00000164508	Chromatin interaction
ENSG00000169045	Chromatin interaction
ENSG00000251211	Chromatin interaction
ENSG00000145912	Chromatin interaction
ENSG00000161011	Chromatin interaction
ENSG00000050767	Chromatin interaction
ENSG00000151876	Chromatin interaction
ENSG00000167658	Chromatin interaction
ENSG00000168298	Chromatin interaction
ENSG00000169220	Chromatin interaction
ENSG00000145916	Chromatin interaction
ENSG00000234028	Chromatin interaction
ENSG00000172071	Chromatin interaction
ENSG00000113240	Chromatin interaction
ENSG00000121068	Chromatin interaction
ENSG00000183258	Chromatin interaction
ENSG00000185716	Chromatin interaction
ENSG00000145911	Chromatin interaction
ENSG00000168675	Chromatin interaction
ENSG00000146047	Chromatin interaction
ENSG00000267131	Chromatin interaction
ENSG00000184840	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs2913747	1.00[ASN][1000 genomes]
rs2913749	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs2913752	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2913753	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2913862	0.94[ASN][1000 genomes]
rs2913864	0.94[ASN][1000 genomes]
rs2913865	0.94[ASN][1000 genomes]
rs2913867	0.92[ASN][1000 genomes]
rs2961675	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2961676	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2961677	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2961679	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2961682	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs2961685	1.00[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2961686	1.00[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs9329138	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948342	chr5:177384542-178168737	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	141 gene(s)	inside rSNPs	diseases
2	nsv1029398	chr5:177502106-178070654	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	136 gene(s)	inside rSNPs	diseases
3	nsv1019404	chr5:177507080-177859089	Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	126 gene(s)	inside rSNPs	diseases
4	nsv1017664	chr5:177578194-177633116	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	93 gene(s)	inside rSNPs	diseases
5	nsv482872	chr5:177580298-177744381	Active TSS Strong transcription Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	106 gene(s)	inside rSNPs	diseases
6	nsv1021981	chr5:177620372-177825272	Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	105 gene(s)	inside rSNPs	diseases
7	nsv537967	chr5:177620372-177825272	Active TSS Strong transcription Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic 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	105 gene(s)	inside rSNPs	diseases
8	esv3404661	chr5:177629746-177634244	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	86 gene(s)	inside rSNPs	diseases
9	esv3357614	chr5:177630371-177632919	Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	86 gene(s)	inside rSNPs	diseases
10	nsv820182	chr5:177630926-177634191	Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	84 gene(s)	inside rSNPs	diseases
11	esv3373194	chr5:177630971-177633519	Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	84 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	chr5:177630200-177632600	Active TSS	H9 Cell Line	embryonic stem cell
2	chr5:177630200-177632600	Active TSS	Hela-S3	cervix
3	chr5:177630600-177632600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr5:177630600-177632800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr5:177630800-177632600	Active TSS	H1 Cell Line	embryonic stem cell
6	chr5:177630800-177632600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:177630800-177632600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr5:177630800-177632600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr5:177630800-177632600	Active TSS	HUES48 Cell Line	embryonic stem cell
10	chr5:177630800-177632600	Active TSS	iPS-15b Cell Line	embryonic stem cell
11	chr5:177630800-177632600	Active TSS	iPS-18 Cell Line	embryonic stem cell
12	chr5:177630800-177632600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr5:177630800-177632600	Active TSS	Breast Myoepithelial Primary Cells	Breast
14	chr5:177630800-177632600	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
15	chr5:177630800-177632600	Active TSS	Primary T helper naive cells from peripheral blood	blood
16	chr5:177630800-177632600	Active TSS	Primary T helper cells PMA-I stimulated	--
17	chr5:177630800-177632600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr5:177630800-177632600	Active TSS	Primary T killer naive cells fromperipheralblood	blood
19	chr5:177630800-177632600	Active TSS	Muscle Satellite Cultured Cells	--
20	chr5:177630800-177632600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr5:177630800-177632600	Active TSS	Brain Angular Gyrus	brain
22	chr5:177630800-177632600	Active TSS	Brain Anterior Caudate	brain
23	chr5:177630800-177632600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
24	chr5:177630800-177632600	Active TSS	Brain Substantia Nigra	brain
25	chr5:177630800-177632600	Active TSS	Colon Smooth Muscle	Colon
26	chr5:177630800-177632600	Active TSS	Fetal Brain Female	brain
27	chr5:177630800-177632600	Active TSS	Fetal Intestine Large	intestine
28	chr5:177630800-177632600	Active TSS	Fetal Intestine Small	intestine
29	chr5:177630800-177632600	Active TSS	Fetal Lung	lung
30	chr5:177630800-177632600	Active TSS	Fetal Stomach	stomach
31	chr5:177630800-177632600	Active TSS	Rectal Mucosa Donor 31	rectum
32	chr5:177630800-177632600	Active TSS	A549	lung
33	chr5:177630800-177632600	Active TSS	GM12878-XiMat	blood
34	chr5:177630800-177632600	Active TSS	NHDF-Ad	bronchial
35	chr5:177630800-177632800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr5:177630800-177632800	Active TSS	Primary T killer memory cells from peripheral blood	blood
37	chr5:177630800-177632800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr5:177630800-177632800	Active TSS	Fetal Heart	heart
39	chr5:177630800-177632800	Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr5:177630800-177632800	Active TSS	Placenta Amnion	Placenta Amnion
41	chr5:177630800-177632800	Active TSS	Psoas Muscle	Psoas
42	chr5:177630800-177632800	Active TSS	Right Ventricle	heart
43	chr5:177630800-177632800	Active TSS	Thymus	Thymus
44	chr5:177630800-177633000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr5:177630800-177633000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr5:177630800-177633000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr5:177630800-177633000	Active TSS	Brain Inferior Temporal Lobe	brain
48	chr5:177630800-177633000	Active TSS	Fetal Kidney	kidney
49	chr5:177630800-177633000	Active TSS	Ovary	ovary
50	chr5:177630800-177633000	Active TSS	Rectal Smooth Muscle	rectum

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