Variant report

Variant	rs7789085
Chromosome Location	chr7:100472826-100472827
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:509)
CpG islands
(count:0)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:509 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	PBX3	chr7:100472298-100472981	A549	lung:	n/a	n/a
2	POLR2A	chr7:100471892-100473338	NB4	blood:	n/a	n/a
3	ZBTB33	chr7:100472030-100472929	A549	lung:	n/a	n/a
4	EP300	chr7:100472047-100473097	ECC-1	luminal epithelium:	n/a	chr7:100473013-100473022 chr7:100473078-100473094
5	JUN	chr7:100471425-100473881	K562	blood:	n/a	n/a
6	YY1	chr7:100471680-100473338	SK-N-SH	brain:	n/a	chr7:100473078-100473089 chr7:100472952-100472963
7	TAF1	chr7:100472410-100472945	GM12891	blood:	n/a	n/a
8	POLR2A	chr7:100471606-100473350	GM18505	blood:	n/a	n/a
9	CREB1	chr7:100472154-100473515	HepG2	liver:	n/a	n/a
10	SRF	chr7:100472450-100472842	GM12878	blood:	n/a	n/a
11	MAZ	chr7:100472372-100472929	Hela-S3	cervix:	n/a	n/a
12	MAZ	chr7:100472179-100473279	GM12878	blood:	n/a	n/a
13	CREB1	chr7:100472320-100473018	H1-hESC	embryonic stem cell:	n/a	n/a
14	THAP1	chr7:100472466-100472949	K562	blood:	n/a	n/a
15	POLR2A	chr7:100471347-100473431	ECC-1	luminal epithelium:	n/a	n/a
16	POLR2A	chr7:100472226-100473339	MCF-7	breast:	n/a	n/a
17	POLR2A	chr7:100471510-100473062	HCT-116	colon:	n/a	n/a
18	FOXP2	chr7:100472310-100472988	PFSK-1	brain:	n/a	n/a
19	EP300	chr7:100472485-100472870	T-47D	breast:	n/a	n/a
20	HA-E2F1	chr7:100472403-100473165	Hela-S3	cervix:	n/a	chr7:100472982-100472994 chr7:100473009-100473018 chr7:100473013-100473022
21	MYC	chr7:100472451-100472855	MCF-7	breast:	n/a	n/a
22	MAX	chr7:100472350-100472972	HepG2	liver:	n/a	n/a
23	IRF1	chr7:100472116-100473006	K562	blood:	n/a	chr7:100472642-100472656
24	GTF2F1	chr7:100472099-100472933	Hela-S3	cervix:	n/a	n/a
25	NFIC	chr7:100472076-100473037	GM12878	blood:	n/a	n/a
26	POLR2A	chr7:100472145-100473504	H1-neurons	neurons:	n/a	n/a
27	MYC	chr7:100472268-100472939	K562	blood:	n/a	n/a
28	ZBTB33	chr7:100472189-100472993	HCT-116	colon:	n/a	n/a
29	MAZ	chr7:100472196-100473274	K562	blood:	n/a	n/a
30	RUNX3	chr7:100472133-100472981	GM12878	blood:	n/a	n/a
31	POU2F2	chr7:100472033-100472883	GM12878	blood:	n/a	chr7:100472264-100472278
32	ZBTB33	chr7:100472281-100472894	K562	blood:	n/a	n/a
33	ZBTB7A	chr7:100472341-100472829	HepG2	liver:	n/a	chr7:100472649-100472656
34	SRF	chr7:100472036-100473128	MCF-7	breast:	n/a	n/a
35	YY1	chr7:100471752-100472975	GM12878	blood:	n/a	chr7:100472952-100472963
36	TAF1	chr7:100472107-100472996	K562	blood:	n/a	n/a
37	POLR2A	chr7:100472252-100472899	HepG2	liver:	n/a	n/a
38	MAX	chr7:100472200-100473017	K562	blood:	n/a	n/a
39	ETS1	chr7:100472293-100472855	GM12878	blood:	n/a	chr7:100472515-100472524
40	TAF1	chr7:100472350-100472942	HepG2	liver:	n/a	n/a
41	MAZ	chr7:100472343-100473196	HepG2	liver:	n/a	n/a
42	E2F1	chr7:100472417-100473244	Hela-S3	cervix:	n/a	chr7:100472982-100472994 chr7:100473009-100473018 chr7:100473013-100473022
43	ZBTB7A	chr7:100472255-100472999	K562	blood:	n/a	chr7:100472971-100472979 chr7:100472649-100472656
44	TCF12	chr7:100472261-100472951	GM12878	blood:	n/a	n/a
45	ZBTB33	chr7:100472378-100472869	HepG2	liver:	n/a	n/a
46	POLR2A	chr7:100471608-100473384	H1-hESC	embryonic stem cell:	n/a	n/a
47	REST	chr7:100472666-100472898	GM12878	blood:	n/a	n/a
48	POU2F2	chr7:100472017-100473038	GM12878	blood:	n/a	chr7:100472264-100472278
49	POLR2A	chr7:100471933-100473420	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr7:100472161-100473147	HEK293	kidney:	n/a	n/a

No data

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:100448186..100450905-chr7:100471509..100474207,3	K562	blood:
2	chr17:56708882..56709843-chr7:100472298..100473076,2	MCF-7	breast:
3	chr7:100472344..100473067-chr7:100487033..100488215,3	MCF-7	breast:
4	chr10:101945522..101946120-chr7:100472805..100473326,2	HCT-116	colon:
5	chr7:100470889..100475047-chr7:100805272..100809585,4	MCF-7	breast:
6	chr7:100083221..100085283-chr7:100471464..100473239,2	K562	blood:
7	chr7:100410860..100413400-chr7:100471850..100474655,4	MCF-7	breast:
8	chr6:26251387..26252142-chr7:100472118..100473007,2	Hela-S3	cervix:
9	chr7:100471127..100473629-chr7:100728368..100730220,3	K562	blood:
10	chr17:7819184..7819934-chr7:100472765..100473448,2	Hela-S3	cervix:
11	chr2:232573730..232575283-chr7:100471498..100474384,2	MCF-7	breast:
12	chr1:45240926..45241735-chr7:100472754..100473340,2	NB4	blood:
13	chr7:100285374..100287070-chr7:100470986..100472980,2	K562	blood:
14	chr7:100301991..100304914-chr7:100472265..100475755,3	MCF-7	breast:
15	chr1:8085834..8086462-chr7:100472148..100473122,2	Hela-S3	cervix:
16	chr7:100452256..100454865-chr7:100471094..100473854,2	K562	blood:
17	chr7:100470857..100473840-chr8:103875332..103878147,2	K562	blood:
18	chr7:100422126..100425537-chr7:100471170..100475559,4	MCF-7	breast:
19	chr7:100450381..100452181-chr7:100471838..100473668,2	K562	blood:
20	chr14:75745173..75745996-chr7:100472052..100473041,2	Hela-S3	cervix:
21	chr7:100471774..100474395-chr7:100608016..100610149,2	K562	blood:
22	chr7:100025223..100027930-chr7:100471250..100474138,3	MCF-7	breast:
23	chr7:100284400..100287604-chr7:100471903..100474319,4	MCF-7	breast:
24	chr7:100182521..100184068-chr7:100470982..100473122,2	K562	blood:
25	chr1:11967269..11969054-chr7:100472288..100474008,2	MCF-7	breast:
26	chr7:100471473..100474219-chr7:100797756..100799384,2	MCF-7	breast:
27	chr19:8386101..8386747-chr7:100472302..100472847,2	Hela-S3	cervix:
28	chr7:100472301..100473124-chrX:130036676..130037344,2	Hela-S3	cervix:
29	chr7:100448750..100454655-chr7:100469427..100474218,6	MCF-7	breast:
30	chr7:100181643..100184250-chr7:100471958..100474283,2	MCF-7	breast:
31	chr16:89118833..89119388-chr7:100472388..100473238,2	Hela-S3	cervix:
32	chr3:186500862..186501482-chr7:100472699..100473269,2	Hela-S3	cervix:
33	chr7:100472601..100475489-chr7:100805185..100810298,4	MCF-7	breast:

No data

Variant related genes	Relation type
SRRT	TF binding region
ENSG00000165675	Chromatin interaction
ENSG00000264294	Chromatin interaction
ENSG00000179859	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000146834	Chromatin interaction
ENSG00000142937	Chromatin interaction
ENSG00000166924	Chromatin interaction
ENSG00000146828	Chromatin interaction
ENSG00000187514	Chromatin interaction
ENSG00000128564	Chromatin interaction
ENSG00000169871	Chromatin interaction
ENSG00000169894	Chromatin interaction
ENSG00000172336	Chromatin interaction
ENSG00000196411	Chromatin interaction
ENSG00000236305	Chromatin interaction
ENSG00000167774	Chromatin interaction
ENSG00000199347	Chromatin interaction
ENSG00000253320	Chromatin interaction
ENSG00000176125	Chromatin interaction
ENSG00000106367	Chromatin interaction
ENSG00000146830	Chromatin interaction
ENSG00000078487	Chromatin interaction
ENSG00000106336	Chromatin interaction
ENSG00000107566	Chromatin interaction
ENSG00000256982	Chromatin interaction
ENSG00000116285	Chromatin interaction
ENSG00000197459	Chromatin interaction
ENSG00000233927	Chromatin interaction
ENSG00000225721	Chromatin interaction
ENSG00000156976	Chromatin interaction
ENSG00000077454	Chromatin interaction
ENSG00000155096	Chromatin interaction
ENSG00000170345	Chromatin interaction
ENSG00000225946	Chromatin interaction
ENSG00000267855	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs12535629	1.00[ASW][hapmap];0.87[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];0.94[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12538287	1.00[ASW][hapmap];0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2075756	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3808356	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3847067	1.00[ASW][hapmap];0.95[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.87[YRI][hapmap];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4727468	0.83[CHB][hapmap];0.86[JPT][hapmap]
rs6955197	0.90[ASN][1000 genomes]
rs7384255	0.90[ASN][1000 genomes]
rs7782299	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7784933	1.00[ASW][hapmap];0.87[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7794216	0.82[EUR][1000 genomes]
rs7800241	1.00[ASW][hapmap];0.91[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[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	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
2	nsv1020837	chr7:100313122-100508635	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
3	esv1832517	chr7:100355490-100749246	Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Enhancers Weak transcription 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 miRNA target site	96 gene(s)	inside rSNPs	diseases
4	esv2758125	chr7:100355490-100749246	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
5	esv2759547	chr7:100355490-100749246	Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
6	nsv464647	chr7:100374087-100497131	Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
7	nsv607965	chr7:100374087-100497131	Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
8	nsv1032673	chr7:100382250-100606794	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
9	nsv888797	chr7:100386900-100482026	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
10	nsv888798	chr7:100406144-100472826	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
11	nsv888799	chr7:100406144-100497131	Enhancers Bivalent Enhancer Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
12	nsv888801	chr7:100416250-100497131	Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
13	nsv464648	chr7:100422156-100518458	Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
14	nsv607966	chr7:100422156-100518458	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
15	nsv831073	chr7:100425659-100544888	Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7789085	FAM185A	cis	cerebellum	SCAN
rs7789085	TRRAP	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100471400-100474800	Transcr. at gene 5' and 3'	Dnd41	blood
2	chr7:100471600-100474000	Active TSS	iPS-15b Cell Line	embryonic stem cell
3	chr7:100471800-100473400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr7:100471800-100473400	Active TSS	Thymus	Thymus
5	chr7:100471800-100473600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
6	chr7:100471800-100473800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr7:100471800-100474000	Active TSS	iPS-20b Cell Line	embryonic stem cell
8	chr7:100471800-100474200	Active TSS	H1 Cell Line	embryonic stem cell
9	chr7:100471800-100474200	Active TSS	HUES48 Cell Line	embryonic stem cell
10	chr7:100471800-100474400	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr7:100472000-100473000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr7:100472000-100473200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
13	chr7:100472000-100473600	Active TSS	Aorta	Aorta
14	chr7:100472000-100473600	Active TSS	Colonic Mucosa	Colon
15	chr7:100472000-100473600	Active TSS	Gastric	stomach
16	chr7:100472000-100473600	Active TSS	Ovary	ovary
17	chr7:100472000-100473600	Active TSS	Placenta Amnion	Placenta Amnion
18	chr7:100472000-100473600	Active TSS	Right Ventricle	heart
19	chr7:100472000-100473800	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr7:100472000-100473800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr7:100472000-100473800	Active TSS	iPS-18 Cell Line	embryonic stem cell
22	chr7:100472000-100473800	Active TSS	Fetal Kidney	kidney
23	chr7:100472000-100473800	Active TSS	Right Atrium	heart
24	chr7:100472000-100474000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr7:100472000-100474200	Active TSS	H9 Cell Line	embryonic stem cell
26	chr7:100472000-100474200	Active TSS	Psoas Muscle	Psoas
27	chr7:100472000-100474400	Active TSS	HSMMtube	muscle
28	chr7:100472200-100473200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr7:100472200-100473200	Active TSS	Primary T cells from cord blood	blood
30	chr7:100472200-100473200	Active TSS	Brain Angular Gyrus	brain
31	chr7:100472200-100473200	Active TSS	Brain Cingulate Gyrus	brain
32	chr7:100472200-100473200	Active TSS	Colon Smooth Muscle	Colon
33	chr7:100472200-100473200	Active TSS	Fetal Brain Male	brain
34	chr7:100472200-100473200	Active TSS	Left Ventricle	heart
35	chr7:100472200-100473200	Active TSS	Stomach Smooth Muscle	stomach
36	chr7:100472200-100473400	Active TSS	Primary T killer memory cells from peripheral blood	blood
37	chr7:100472200-100473400	Active TSS	Brain Anterior Caudate	brain
38	chr7:100472200-100473400	Active TSS	Brain Inferior Temporal Lobe	brain
39	chr7:100472200-100473400	Active TSS	Brain Substantia Nigra	brain
40	chr7:100472200-100473400	Active TSS	Fetal Brain Female	brain
41	chr7:100472200-100473400	Active TSS	Fetal Heart	heart
42	chr7:100472200-100473400	Active TSS	Fetal Stomach	stomach
43	chr7:100472200-100473400	Active TSS	Rectal Smooth Muscle	rectum
44	chr7:100472200-100473400	Active TSS	Sigmoid Colon	Sigmoid Colon
45	chr7:100472200-100473400	Active TSS	Spleen	Spleen
46	chr7:100472200-100473600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr7:100472200-100473600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr7:100472200-100473600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
49	chr7:100472200-100473600	Active TSS	Lung	lung
50	chr7:100472200-100473600	Active TSS	Small Intestine	intestine

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