Variant report

Variant	rs60844404
Chromosome Location	chr7:100080474-100080475
allele	A/T
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	ZNF143	chr7:100080340-100081314	K562	blood:	n/a	chr7:100080940-100080950 chr7:100080880-100080898 chr7:100081075-100081093 chr7:100080933-100080951
2	RCOR1	chr7:100080427-100081192	Hela-S3	cervix:	n/a	n/a
3	ZNF143	chr7:100080410-100080600	Hela-S3	cervix:	n/a	n/a
4	ELF1	chr7:100080422-100081319	GM12878	blood:	n/a	chr7:100081078-100081090 chr7:100080779-100080791
5	HDAC2	chr7:100080288-100080653	K562	blood:	n/a	n/a
6	CTCF	chr7:100080420-100080570	NHDF-neo	bronchial:	n/a	n/a
7	NR2F2	chr7:100080409-100081361	MCF-7	breast:	n/a	chr7:100080792-100080807
8	CTCF	chr7:100080400-100080550	HRPEpiC	eye:	n/a	n/a
9	CTCF	chr7:100080400-100080690	GM12864	blood:	n/a	n/a
10	JUN	chr7:100080414-100081490	K562	blood:	n/a	chr7:100080711-100080720
11	CTCF	chr7:100080400-100080550	HPF	lung:	n/a	n/a
12	RCOR1	chr7:100080345-100081297	K562	blood:	n/a	n/a
13	NR2F2	chr7:100080312-100081374	HepG2	liver:	n/a	chr7:100080792-100080807
14	NR2F2	chr7:100080368-100081182	K562	blood:	n/a	chr7:100080792-100080807
15	RAD21	chr7:100080414-100082796	SK-N-SH	brain:	n/a	chr7:100081042-100081061 chr7:100080972-100080991 chr7:100080936-100080945 chr7:100081192-100081206 chr7:100080937-100080947 chr7:100081043-100081057
16	CTCF	chr7:100080340-100080490	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr7:100080440-100080590	HepG2	liver:	n/a	n/a
18	NR2F2	chr7:100080413-100081297	K562	blood:	n/a	chr7:100080792-100080807
19	SMARCB1	chr7:100080467-100081258	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr7:100080277-100081151	K562	blood:	n/a	n/a
21	ZNF143	chr7:100080410-100080635	H1-hESC	embryonic stem cell:	n/a	n/a
22	SMC3	chr7:100080427-100081474	SK-N-SH	brain:	n/a	chr7:100080933-100080947 chr7:100080976-100080990 chr7:100081046-100081060 chr7:100080937-100080947
23	MAX	chr7:100080317-100081757	MCF-7	breast:	n/a	chr7:100081185-100081194
24	CTCF	chr7:100080400-100080550	AoAF	blood vessel:	n/a	n/a
25	CTCF	chr7:100080440-100080590	A549	lung:	n/a	n/a
26	CTCF	chr7:100080167-100082239	SK-N-SH	brain:	n/a	chr7:100080980-100080989 chr7:100081046-100081059 chr7:100080936-100080946 chr7:100081963-100081972 chr7:100080974-100080992 chr7:100081050-100081059 chr7:100081044-100081062 chr7:100081045-100081061 chr7:100080977-100080987 chr7:100082002-100082012 chr7:100080934-100080947 chr7:100080931-100080944
27	CTCF	chr7:100080193-100081477	A549	lung:	n/a	chr7:100080980-100080989 chr7:100081046-100081059 chr7:100080936-100080946 chr7:100080974-100080992 chr7:100081050-100081059 chr7:100081044-100081062 chr7:100081045-100081061 chr7:100080977-100080987 chr7:100080934-100080947 chr7:100080931-100080944
28	CTCF	chr7:100080400-100080550	GM12867	blood:	n/a	n/a
29	RCOR1	chr7:100080439-100081224	K562	blood:	n/a	n/a
30	CTCF	chr7:100080460-100080610	HA-sp	spinal cord:	n/a	n/a
31	CTCF	chr7:100080420-100080570	HPF	lung:	n/a	n/a
32	MAZ	chr7:100080400-100081876	IMR90	lung:	n/a	chr7:100081185-100081194
33	MAX	chr7:100080283-100081703	K562	blood:	n/a	chr7:100081185-100081194
34	MAX	chr7:100080308-100081782	HepG2	liver:	n/a	chr7:100081185-100081194

No.	Distal block	Cell Line	Cell type
1	chr7:100080109..100082832-chr7:100180830..100183809,4	MCF-7	breast:
2	chr20:45925390..45926255-chr7:100080190..100081125,2	MCF-7	breast:
3	chr7:100080256..100081975-chr7:100135714..100137947,2	MCF-7	breast:
4	chr7:100078512..100081448-chr7:100177451..100180424,2	MCF-7	breast:
5	chr7:100073820..100078843-chr7:100079329..100083762,6	MCF-7	breast:
6	chr7:100074425..100078694-chr7:100079448..100083758,11	K562	blood:
7	chr7:100032559..100034120-chr7:100079176..100081080,2	K562	blood:
8	chr7:100024700..100032514-chr7:100067180..100083143,31	K562	blood:
9	chr7:100022010..100030260-chr7:100068697..100082544,31	K562	blood:
10	chr7:100079431..100084153-chr7:100084209..100089579,10	K562	blood:
11	chr7:100080163..100084843-chr7:100085212..100090254,7	MCF-7	breast:

Variant related genes	Relation type
NYAP1	TF binding region
TSC22D4	TF binding region
ENSG00000241357	Chromatin interaction
ENSG00000077454	Chromatin interaction
ENSG00000160813	Chromatin interaction
ENSG00000166925	Chromatin interaction
ENSG00000078487	Chromatin interaction
ENSG00000106351	Chromatin interaction
ENSG00000146834	Chromatin interaction
ENSG00000166924	Chromatin interaction
ENSG00000240211	Chromatin interaction
ENSG00000106336	Chromatin interaction

Extended variants
information (count: 67 )
Associated
traits (count: 43 )

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs1073	1.00[ASN][1000 genomes]
rs11559117	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11760536	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11761624	1.00[ASN][1000 genomes]
rs11761725	1.00[ASN][1000 genomes]
rs11761784	1.00[ASN][1000 genomes]
rs11763511	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11764818	1.00[ASN][1000 genomes]
rs11766202	1.00[ASN][1000 genomes]
rs11766752	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11769700	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11772580	1.00[ASN][1000 genomes]
rs11773661	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1962269	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2406253	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2406255	1.00[ASN][1000 genomes]
rs28629346	1.00[ASN][1000 genomes]
rs2897358	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34989573	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4074838	1.00[ASN][1000 genomes]
rs4385401	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4463351	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4469386	1.00[ASN][1000 genomes]
rs4472444	0.80[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4989959	1.00[ASN][1000 genomes]
rs60257855	1.00[ASN][1000 genomes]
rs60478351	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60644673	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66648318	1.00[ASN][1000 genomes]
rs66958101	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67040465	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs67196635	1.00[ASN][1000 genomes]
rs67239991	1.00[ASN][1000 genomes]
rs67483801	1.00[ASN][1000 genomes]
rs67885733	1.00[ASN][1000 genomes]
rs6948699	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6953107	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6955362	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6962151	1.00[ASN][1000 genomes]
rs6972167	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6974286	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6975514	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6975729	1.00[ASN][1000 genomes]
rs6978739	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6979335	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73405353	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7787620	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7787825	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7794485	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7800667	1.00[ASN][1000 genomes]
rs7809801	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7811142	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3350965	chr7:99747460-100146105	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	304 gene(s)	inside rSNPs	diseases
2	esv1829095	chr7:99814675-100494084	Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	393 gene(s)	inside rSNPs	diseases
3	nsv831071	chr7:99918025-100113413	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers 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 miRNA target site	287 gene(s)	inside rSNPs	diseases
4	nsv888776	chr7:100014711-100198386	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	297 gene(s)	inside rSNPs	diseases
5	nsv888777	chr7:100014711-100221867	Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	304 gene(s)	inside rSNPs	diseases
6	nsv888778	chr7:100014711-100236593	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	310 gene(s)	inside rSNPs	diseases
7	nsv888779	chr7:100014711-100313420	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	321 gene(s)	inside rSNPs	diseases
8	nsv888780	chr7:100032665-100198386	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
9	nsv527050	chr7:100056166-100125975	Strong transcription Weak transcription Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
10	nsv888781	chr7:100060928-100097895	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
11	nsv888782	chr7:100064719-100236593	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers 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 target site	74 gene(s)	inside rSNPs	diseases
12	nsv888783	chr7:100073292-100136241	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
13	nsv888784	chr7:100076614-100097895	Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
14	esv3375220	chr7:100080241-100082789	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases
15	esv3381694	chr7:100080416-100082564	Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:43)

SNP	Gene	Cis/trans	Tissue	Source
rs60844404	PILRB	Cis_1M	lymphoblastoid	RTeQTL
rs60844404	PVRIG2P	cis	Artery Tibial	GTEx
rs60844404	PILRA	cis	Thyroid	GTEx
rs60844404	PILRB	cis	Nerve Tibial	GTEx
rs60844404	PVRIG2P	cis	Esophagus Mucosa	GTEx
rs60844404	PILRB	cis	Adipose Subcutaneous	GTEx
rs60844404	PILRA	cis	Esophagus Muscularis	GTEx
rs60844404	PILRB	cis	multi-tissue	Pritchard
rs60844404	ZCWPW1	cis	Nerve Tibial	GTEx
rs60844404	STAG3L5P	cis	Esophagus Mucosa	GTEx
rs60844404	STAG3L5P	cis	Nerve Tibial	GTEx
rs60844404	STAG3L5P	cis	Stomach	GTEx
rs60844404	PILRA	cis	Heart Left Ventricle	GTEx
rs60844404	PILRB	cis	Whole Blood	GTEx
rs60844404	PILRB	cis	Artery Aorta	GTEx
rs60844404	PILRA	cis	Artery Tibial	GTEx
rs60844404	PILRB	cis	Skin Sun Exposed Lower leg	GTEx
rs60844404	PILRB	cis	Esophagus Muscularis	GTEx
rs60844404	PILRA	cis	Adipose Subcutaneous	GTEx
rs60844404	PILRB	cis	Esophagus Mucosa	GTEx
rs60844404	PILRB	cis	Muscle Skeletal	GTEx
rs60844404	PILRA	cis	Skin Sun Exposed Lower leg	GTEx
rs60844404	PILRA	cis	Nerve Tibial	GTEx
rs60844404	STAG3L5P	cis	Adipose Subcutaneous	GTEx
rs60844404	PVRIG	Cis_1M	lymphoblastoid	RTeQTL
rs60844404	PVRIG2P	cis	Thyroid	GTEx
rs60844404	STAG3L5P	cis	Skin Sun Exposed Lower leg	GTEx
rs60844404	PILRA	cis	Muscle Skeletal	GTEx
rs60844404	STAG3L5P	cis	Artery Tibial	GTEx
rs60844404	PMS2P1	cis	Thyroid	GTEx
rs60844404	STAG3L5P	cis	Heart Left Ventricle	GTEx
rs60844404	PILRA	cis	Artery Aorta	GTEx
rs60844404	PVRIG2P	cis	lung	GTEx
rs60844404	PILRB	cis	lung	GTEx
rs60844404	PILRB	cis	Heart Left Ventricle	GTEx
rs60844404	PILRB	cis	Artery Tibial	GTEx
rs60844404	PILRB	cis	Thyroid	GTEx
rs60844404	STAG3L5P	cis	Artery Aorta	GTEx
rs60844404	STAG3L5P	cis	Muscle Skeletal	GTEx
rs60844404	STAG3L5P	cis	Thyroid	GTEx
rs60844404	STAG3L5P	cis	lung	GTEx
rs60844404	STAG3L5P	cis	Esophagus Muscularis	GTEx
rs60844404	PILRA	cis	Esophagus Mucosa	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100077200-100080600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr7:100077400-100080600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:100077400-100080600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:100077400-100080600	Weak transcription	Aorta	Aorta
5	chr7:100077600-100080600	Weak transcription	Fetal Brain Male	brain
6	chr7:100079200-100080600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr7:100079800-100080600	Enhancers	Thymus	Thymus
8	chr7:100080000-100080600	Enhancers	Primary B cells from peripheral blood	blood
9	chr7:100080000-100080600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr7:100080000-100080800	Flanking Bivalent TSS/Enh	HepG2	liver
11	chr7:100080000-100081000	Flanking Active TSS	Primary B cells from cord blood	blood
12	chr7:100080200-100080600	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr7:100080200-100080600	Enhancers	Esophagus	oesophagus
14	chr7:100080200-100080600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr7:100080200-100080600	Enhancers	Fetal Muscle Trunk	muscle
16	chr7:100080200-100080600	Enhancers	Fetal Thymus	thymus
17	chr7:100080200-100080600	Enhancers	Ovary	ovary
18	chr7:100080200-100080800	Flanking Active TSS	Hela-S3	cervix
19	chr7:100080200-100080800	Flanking Active TSS	K562	blood
20	chr7:100080200-100081000	Enhancers	Fetal Lung	lung
21	chr7:100080200-100081000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
22	chr7:100080200-100082000	Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr7:100080400-100080600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
24	chr7:100080400-100080600	Flanking Active TSS	H1 Cell Line	embryonic stem cell
25	chr7:100080400-100080600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr7:100080400-100080600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr7:100080400-100080600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
28	chr7:100080400-100080600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
29	chr7:100080400-100080600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
30	chr7:100080400-100080600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr7:100080400-100080600	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr7:100080400-100080600	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr7:100080400-100080600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
34	chr7:100080400-100080600	Enhancers	Brain Substantia Nigra	brain
35	chr7:100080400-100080600	Enhancers	Colon Smooth Muscle	Colon
36	chr7:100080400-100080600	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr7:100080400-100080600	Enhancers	Fetal Muscle Leg	muscle
38	chr7:100080400-100080600	Enhancers	Placenta	Placenta
39	chr7:100080400-100080600	Enhancers	Fetal Stomach	stomach
40	chr7:100080400-100080600	Enhancers	Left Ventricle	heart
41	chr7:100080400-100080600	Enhancers	Pancreas	Pancrea
42	chr7:100080400-100080600	Enhancers	Psoas Muscle	Psoas
43	chr7:100080400-100080600	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr7:100080400-100080600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
45	chr7:100080400-100080600	Enhancers	Small Intestine	intestine
46	chr7:100080400-100080600	Flanking Active TSS	Spleen	Spleen
47	chr7:100080400-100080600	Flanking Active TSS	A549	lung
48	chr7:100080400-100080600	Enhancers	NH-A	brain
49	chr7:100080400-100080600	Flanking Active TSS	NHDF-Ad	bronchial
50	chr7:100080400-100080800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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