Variant report

Variant	esv1814707
Chromosome Location	chr7:6892731-7023265
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1745)
CpG islands
(count:2137)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1745 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:6995667-6996128	K562	blood:	n/a	n/a
2	ATF1	chr7:6962881-6963081	K562	blood:	n/a	n/a
3	BACH1	chr7:6897551-6897628	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr7:6911365-6911638	GM12878	blood:	n/a	n/a
5	BATF	chr7:6970367-6970679	GM12878	blood:	n/a	n/a
6	BATF	chr7:6967768-6968127	GM12878	blood:	n/a	n/a
7	BATF	chr7:6959520-6959921	GM12878	blood:	n/a	chr7:6959720-6959731
8	BATF	chr7:6897373-6897774	GM12878	blood:	n/a	n/a
9	BATF	chr7:6967778-6968070	GM12878	blood:	n/a	n/a
10	BATF	chr7:6930048-6930266	GM12878	blood:	n/a	chr7:6930144-6930155
11	BATF	chr7:7004618-7004964	GM12878	blood:	n/a	n/a
12	BATF	chr7:6959640-6959863	GM12878	blood:	n/a	chr7:6959720-6959731
13	BATF	chr7:6993800-6993986	GM12878	blood:	n/a	n/a
14	BATF	chr7:6965792-6966222	GM12878	blood:	n/a	n/a
15	BATF	chr7:6992805-6993006	GM12878	blood:	n/a	n/a
16	BATF	chr7:6967256-6967613	GM12878	blood:	n/a	n/a
17	BATF	chr7:6911459-6911623	GM12878	blood:	n/a	n/a
18	BATF	chr7:6965828-6966219	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:7004553-7004898	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:6966697-6966858	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:6968204-6968549	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:6897283-6897636	GM12878	blood:	n/a	chr7:6897421-6897434
23	BCL11A	chr7:6967360-6967540	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:6970443-6970693	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:6967281-6967607	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:6965815-6966145	GM12878	blood:	n/a	chr7:6966028-6966037
27	BCL11A	chr7:6965764-6966259	GM12878	blood:	n/a	chr7:6966028-6966037
28	BCL3	chr7:6928564-6929398	GM12878	blood:	n/a	n/a
29	BCL3	chr7:6916434-6916785	GM12878	blood:	n/a	n/a
30	BCL3	chr7:6928637-6929472	GM12878	blood:	n/a	n/a
31	BCLAF1	chr7:6897456-6897677	GM12878	blood:	n/a	n/a
32	BHLHE40	chr7:6897488-6897590	GM12878	blood:	n/a	n/a
33	BHLHE40	chr7:6968034-6968094	GM12878	blood:	n/a	n/a
34	BHLHE40	chr7:6995939-6996011	K562	blood:	n/a	n/a
35	BHLHE40	chr7:6943039-6943099	GM12878	blood:	n/a	n/a
36	BHLHE40	chr7:6962913-6963006	K562	blood:	n/a	n/a
37	BHLHE40	chr7:6929175-6929309	K562	blood:	n/a	n/a
38	BHLHE40	chr7:6967280-6967585	GM12878	blood:	n/a	n/a
39	CBX3	chr7:6977915-6978267	K562	blood:	n/a	n/a
40	CBX3	chr7:6962801-6963079	K562	blood:	n/a	n/a
41	CBX3	chr7:6940710-6940918	K562	blood:	n/a	n/a
42	CBX3	chr7:6962809-6962993	K562	blood:	n/a	n/a
43	CBX3	chr7:6995674-6996047	K562	blood:	n/a	n/a
44	CBX3	chr7:6965814-6966339	K562	blood:	n/a	n/a
45	CEBPB	chr7:7002641-7002841	A549	lung:	n/a	n/a
46	CEBPB	chr7:7002619-7002711	IMR90	lung:	n/a	n/a
47	CEBPB	chr7:6973611-6973982	HepG2	liver:	n/a	chr7:6973791-6973802
48	CEBPB	chr7:6936030-6936175	A549	lung:	n/a	n/a
49	CEBPB	chr7:6973609-6973984	K562	blood:	n/a	chr7:6973791-6973802
50	CEBPB	chr7:6936027-6936120	K562	blood:	n/a	n/a

(count:2137 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6909121-6909171	AG10803	skin:	n/a
2	chr7:6974956-6975006	NHBE	bronchial:	n/a
3	chr7:6909121-6909171	AG10803	skin:	n/a
4	chr7:6974956-6975006	NHBE	bronchial:	n/a
5	chr7:6914498-6914548	AG09309	skin:	n/a
6	chr7:6979488-6979538	HNPCEpiC	eye:	n/a
7	chr7:6894869-6894919	AG09319	gingival:	n/a
8	chr7:6974892-6974942	BE2_C	brain:	n/a
9	chr7:6909188-6909238	SKMC	muscle:	n/a
10	chr7:6892911-6892961	PFSK-1	brain:	n/a
11	chr7:6915894-6915944	AG04450	lung:	fetal
12	chr7:6895389-6895439	Hepatocyte	liver:	n/a
13	chr7:6892885-6892935	AG04449	skin:	fetal
14	chr7:6974956-6975006	SAEC	small airway:	n/a
15	chr7:6915928-6915978	HAEpiC	amniotic membrane:	n/a
16	chr7:6892911-6892961	GM06990	blood:	n/a
17	chr7:6974892-6974942	AG09319	gingival:	n/a
18	chr7:6974892-6974942	PANC-1	pancreas:	n/a
19	chr7:6911051-6911101	GM12878	blood:	n/a
20	chr7:6974758-6974808	HNPCEpiC	eye:	n/a
21	chr7:7015218-7015268	Hela-S3	cervix:	n/a
22	chr7:6916089-6916139	NT2-D1	testis:	n/a
23	chr7:6915928-6915978	AG04450	lung:	fetal
24	chr7:6974892-6974942	GM12878	blood:	n/a
25	chr7:6895389-6895439	NT2-D1	testis:	n/a
26	chr7:6892911-6892961	Hepatocyte	liver:	n/a
27	chr7:6894477-6894527	IMR90	lung:	fetal
28	chr7:6910741-6910791	BJ	skin:	n/a
29	chr7:6910741-6910791	MCF-7	breast:	n/a
30	chr7:6990107-6990157	HRE	kidney:	n/a
31	chr7:6894477-6894527	ECC-1	luminal epithelium:	n/a
32	chr7:6974758-6974808	NT2-D1	testis:	n/a
33	chr7:6894869-6894919	IMR90	lung:	fetal
34	chr7:6921561-6921611	A549	lung:	n/a
35	chr7:6895389-6895439	AoSMC	blood vessel:	n/a
36	chr7:6893572-6893622	HEK293	kidney:	embryo
37	chr7:6893553-6893603	MCF10A-Er-Src	breast:	n/a
38	chr7:6921561-6921611	H1-hESC	embryonic stem cell:	embryo
39	chr7:6915373-6915423	Jurkat	blood:	n/a
40	chr7:6895389-6895439	NHDF-neo	bronchial:	n/a
41	chr7:6911211-6911261	Hela-S3	cervix:	n/a
42	chr7:6897617-6897667	HIPEpiC	eye:	n/a
43	chr7:6909121-6909171	U87	brain:	n/a
44	chr7:6974270-6974320	GM12892	blood:	n/a
45	chr7:6911051-6911101	PFSK-1	brain:	n/a
46	chr7:6910741-6910791	HIPEpiC	eye:	n/a
47	chr7:6977556-6977606	MCF10A-Er-Src	breast:	n/a
48	chr7:6911051-6911101	HCM	heart:	n/a
49	chr7:6974892-6974942	HepG2	liver:	n/a
50	chr7:6914498-6914548	MCF-7	breast:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:6144018..6145898-chr7:6967333..6970236,2	K562	blood:
2	chr7:6362339..6362861-chr7:6969838..6970665,2	K562	blood:
3	chr7:6629513..6630064-chr7:6897112..6897752,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCZ1B-5	chr7:6963709-6964144	NONHSAT119086

No data

Variant related genes	Relation type
ALG1L5P	TF binding region
ENSG00000241539	TF binding region
ENSG00000243531	TF binding region
UNC93B2	TF binding region
FAM86LP	TF binding region
OR7E136P	TF binding region
ENSG00000263457	TF binding region
OR7E59P	TF binding region
ALG1L5P	CpG island
ENSG00000241539	CpG island
ENSG00000243531	CpG island
UNC93B2	CpG island
FAM86LP	CpG island
OR7E136P	CpG island
ENSG00000263457	CpG island
OR7E59P	CpG island
ENSG00000146576	chromatin interactions
ENSG00000106346	chromatin interactions

Extended variants
information (count: 5894 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:5894 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564412446	chr7:6892735-6892736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs35755706	chr7:6892746-6892747	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs6970094	chr7:6892771-6892772	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs202163685	chr7:6892777-6892778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200202799	chr7:6892782-6892783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572407896	chr7:6892798-6892799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs568006776	chr7:6892810-6892811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143753318	chr7:6892831-6892832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532331743	chr7:6892843-6892844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs151126480	chr7:6892867-6892868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200853945	chr7:6892888-6892889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529791405	chr7:6892899-6892900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6951964	chr7:6892900-6892901	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs6969262	chr7:6892940-6892941	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs368320654	chr7:6892947-6892948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs67520325	chr7:6892958-6892959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570842140	chr7:6892981-6892982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs71524575	chr7:6892984-6892985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs6952149	chr7:6892985-6892986	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs372162763	chr7:6893017-6893018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535534652	chr7:6893018-6893019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201679968	chr7:6893022-6893023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554262477	chr7:6893074-6893075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs62440014	chr7:6893075-6893076	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs189307498	chr7:6893107-6893108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs62440015	chr7:6893136-6893137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577256988	chr7:6893146-6893147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs76336469	chr7:6893154-6893155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560582311	chr7:6893161-6893162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572529136	chr7:6893227-6893228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs62440016	chr7:6893238-6893239	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs199686084	chr7:6893240-6893241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560206325	chr7:6893246-6893247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200754650	chr7:6893259-6893260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527276608	chr7:6893262-6893263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551804771	chr7:6893281-6893282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201892164	chr7:6893282-6893283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62440017	chr7:6893289-6893290	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs62440018	chr7:6893315-6893316	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs550455844	chr7:6893319-6893320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs141802407	chr7:6893320-6893321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536062564	chr7:6893326-6893327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553960288	chr7:6893331-6893332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs73674185	chr7:6893366-6893367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200101350	chr7:6893398-6893399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112543656	chr7:6893401-6893402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558223378	chr7:6893408-6893409	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146186071	chr7:6893417-6893418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544471054	chr7:6893443-6893444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556439755	chr7:6893444-6893445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:498 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6883800-6893800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr7:6886000-6894200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr7:6893400-6893600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:6893800-6894000	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr7:6893800-6894000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr7:6893800-6894200	Enhancers	Esophagus	oesophagus
7	chr7:6893800-6894200	Enhancers	Fetal Intestine Small	intestine
8	chr7:6894000-6894200	Enhancers	Fetal Intestine Large	intestine
9	chr7:6894000-6894200	Enhancers	Stomach Smooth Muscle	stomach
10	chr7:6894000-6894400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr7:6894000-6894400	Enhancers	Colonic Mucosa	Colon
12	chr7:6894200-6894400	Weak transcription	Primary hematopoietic stem cells	blood
13	chr7:6894200-6894400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr7:6894200-6894400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr7:6894200-6894400	Flanking Active TSS	Fetal Intestine Small	intestine
16	chr7:6894200-6894400	Flanking Active TSS	Stomach Smooth Muscle	stomach
17	chr7:6894200-6894600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr7:6894200-6894800	Active TSS	Fetal Intestine Large	intestine
19	chr7:6894400-6894600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr7:6894400-6894600	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr7:6894400-6894600	Enhancers	Primary B cells from cord blood	blood
22	chr7:6894400-6894600	Enhancers	Primary hematopoietic stem cells	blood
23	chr7:6894400-6894600	Active TSS	Primary T helper cells fromperipheralblood	blood
24	chr7:6894400-6894600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr7:6894400-6894600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr7:6894400-6894600	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr7:6894400-6894600	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
28	chr7:6894400-6894600	Enhancers	Stomach Smooth Muscle	stomach
29	chr7:6894400-6894600	Enhancers	HUVEC	blood vessel
30	chr7:6894400-6894800	Active TSS	Right Ventricle	heart
31	chr7:6894400-6895000	Active TSS	Primary B cells from peripheral blood	blood
32	chr7:6894400-6895200	Active TSS	Primary T helper cells PMA-I stimulated	--
33	chr7:6894400-6895200	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
34	chr7:6894400-6895200	Active TSS	Duodenum Mucosa	Duodenum
35	chr7:6894400-6895200	Active TSS	Esophagus	oesophagus
36	chr7:6894400-6895200	Active TSS	Fetal Intestine Small	intestine
37	chr7:6894400-6895200	Active TSS	Ovary	ovary
38	chr7:6894400-6895400	Bivalent/Poised TSS	Primary T regulatory cells fromperipheralblood	blood
39	chr7:6894400-6895400	Active TSS	Cortex derived primary cultured neurospheres	brain
40	chr7:6894400-6895400	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
41	chr7:6894400-6895600	Active TSS	H1 Cell Line	embryonic stem cell
42	chr7:6894400-6895600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr7:6894400-6895600	Active TSS	HUES48 Cell Line	embryonic stem cell
44	chr7:6894400-6895600	Active TSS	HUES6 Cell Line	embryonic stem cell
45	chr7:6894400-6895600	Active TSS	HUES64 Cell Line	embryonic stem cell
46	chr7:6894400-6895600	Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr7:6894400-6895600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr7:6894400-6895600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
49	chr7:6894400-6895600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr7:6894400-6895600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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