Variant report

Variant	nsv606009
Chromosome Location	chr7:6686601-6694679
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:122)
CpG islands
(count:551)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:122 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr7:6693791-6694049	GM12878	blood:	n/a	n/a
2	BCL3	chr7:6693271-6693492	GM12878	blood:	n/a	n/a
3	CCNT2	chr7:6694042-6694139	K562	blood:	n/a	n/a
4	CHD2	chr7:6688733-6688788	Hela-S3	cervix:	n/a	n/a
5	CTCF	chr7:6687900-6688050	HMEC	breast:	n/a	n/a
6	CTCF	chr7:6688074-6688083	MCF-7	breast:	n/a	n/a
7	CTCF	chr7:6688006-6688143	MCF-7	breast:	n/a	n/a
8	CTCF	chr7:6688038-6688147	MCF-7	breast:	n/a	n/a
9	CTCF	chr7:6687960-6688110	SK-N-SH_RA	brain:	n/a	n/a
10	ELF1	chr7:6694512-6694819	GM12878	blood:	n/a	n/a
11	ELF1	chr7:6693518-6693985	GM12878	blood:	n/a	n/a
12	GABPA	chr7:6693265-6693772	H1-hESC	embryonic stem cell:	n/a	n/a
13	GABPA	chr7:6693871-6694198	H1-hESC	embryonic stem cell:	n/a	n/a
14	HMGN3	chr7:6692437-6692466	K562	blood:	n/a	n/a
15	MYC	chr7:6692304-6692375	MCF-7	breast:	n/a	n/a
16	MYC	chr7:6687405-6687481	MCF-7	breast:	n/a	n/a
17	MYC	chr7:6693497-6693638	MCF-7	breast:	n/a	n/a
18	PAX5	chr7:6692203-6692749	GM12878	blood:	n/a	n/a
19	PAX5	chr7:6692302-6692682	GM12878	blood:	n/a	n/a
20	PAX5	chr7:6693823-6694038	GM12892	blood:	n/a	chr7:6693933-6693952
21	PAX5	chr7:6692292-6692760	GM12878	blood:	n/a	n/a
22	PAX5	chr7:6693715-6694061	GM12878	blood:	n/a	chr7:6693933-6693952
23	PAX5	chr7:6692282-6692683	GM12891	blood:	n/a	n/a
24	PAX5	chr7:6693471-6694164	GM12892	blood:	n/a	chr7:6693933-6693952
25	PAX5	chr7:6692399-6692566	GM12878	blood:	n/a	n/a
26	PAX5	chr7:6693543-6694257	GM12878	blood:	n/a	chr7:6693933-6693952
27	PAX5	chr7:6693717-6694116	GM12891	blood:	n/a	chr7:6693933-6693952
28	PAX5	chr7:6692099-6692801	GM12892	blood:	n/a	n/a
29	PAX5	chr7:6693740-6694153	GM12878	blood:	n/a	chr7:6693933-6693952
30	PBX3	chr7:6693289-6693652	GM12878	blood:	n/a	n/a
31	PBX3	chr7:6693877-6694030	GM12878	blood:	n/a	n/a
32	POLR2A	chr7:6690265-6690321	MCF-7	breast:	n/a	n/a
33	POLR2A	chr7:6694257-6694677	GM12878	blood:	n/a	n/a
34	POLR2A	chr7:6688021-6688066	K562	blood:	n/a	n/a
35	POLR2A	chr7:6688459-6688697	K562	blood:	n/a	n/a
36	POLR2A	chr7:6693424-6693453	HUVEC	blood vessel:	n/a	n/a
37	POLR2A	chr7:6694457-6694719	K562	blood:	n/a	n/a
38	POLR2A	chr7:6688660-6688773	K562	blood:	n/a	n/a
39	POLR2A	chr7:6693843-6693956	K562	blood:	n/a	n/a
40	POLR2A	chr7:6687175-6687484	K562	blood:	n/a	n/a
41	POLR2A	chr7:6692595-6692612	K562	blood:	n/a	n/a
42	POLR2A	chr7:6687423-6687440	MCF-7	breast:	n/a	n/a
43	POLR2A	chr7:6688880-6689085	K562	blood:	n/a	n/a
44	POLR2A	chr7:6686825-6687614	GM12878	blood:	n/a	n/a
45	POLR2A	chr7:6690443-6690483	MCF-7	breast:	n/a	n/a
46	POLR2A	chr7:6693971-6693987	MCF-7	breast:	n/a	n/a
47	POLR2A	chr7:6694042-6694952	GM12878	blood:	n/a	n/a
48	POLR2A	chr7:6687682-6687986	K562	blood:	n/a	n/a
49	POLR2A	chr7:6694405-6694634	GM12878	blood:	n/a	n/a
50	POLR2A	chr7:6692412-6692572	K562	blood:	n/a	n/a

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6692445-6692495	HCT-116	colon:	n/a
2	chr7:6693334-6693384	MCF-7	breast:	n/a
3	chr7:6692445-6692495	HCT-116	colon:	n/a
4	chr7:6693334-6693384	MCF-7	breast:	n/a
5	chr7:6692445-6692495	SKMC	muscle:	n/a
6	chr7:6694373-6694423	LNCaP	prostate:	n/a
7	chr7:6692873-6692923	HAEpiC	amniotic membrane:	n/a
8	chr7:6691949-6691999	BE2_C	brain:	n/a
9	chr7:6693838-6693888	AG04449	skin:	fetal
10	chr7:6692445-6692495	HIPEpiC	eye:	n/a
11	chr7:6692873-6692923	T-47D	breast:	n/a
12	chr7:6694373-6694423	A549	lung:	n/a
13	chr7:6692445-6692495	HEK293	kidney:	embryo
14	chr7:6693030-6693080	GM12878	blood:	n/a
15	chr7:6693030-6693080	ProgFib	skin:	n/a
16	chr7:6693334-6693384	HCT-116	colon:	n/a
17	chr7:6692873-6692923	HEEpiC	esophagus:	n/a
18	chr7:6691949-6691999	HRE	kidney:	n/a
19	chr7:6692873-6692923	A549	lung:	n/a
20	chr7:6692873-6692923	ovcar-3	ovarian:	n/a
21	chr7:6690313-6690363	ovcar-3	ovarian:	n/a
22	chr7:6693838-6693888	AoSMC	blood vessel:	n/a
23	chr7:6694373-6694423	HRPEpiC	eye:	n/a
24	chr7:6693334-6693384	SK-N-SH_RA	brain:	n/a
25	chr7:6692445-6692495	GM06990	blood:	n/a
26	chr7:6689218-6689268	SK-N-SH_RA	brain:	n/a
27	chr7:6690313-6690363	Hepatocyte	liver:	n/a
28	chr7:6692873-6692923	HMEC	breast:	n/a
29	chr7:6694373-6694423	HCM	heart:	n/a
30	chr7:6690313-6690363	MCF10A-Er-Src	breast:	n/a
31	chr7:6693334-6693384	SK-N-MC	brain:	n/a
32	chr7:6689218-6689268	AG04450	lung:	fetal
33	chr7:6692445-6692495	Hepatocyte	liver:	n/a
34	chr7:6693334-6693384	MCF10A-Er-Src	breast:	n/a
35	chr7:6694373-6694423	NH-A	brain:	n/a
36	chr7:6689218-6689268	RPTEC	kidney:	n/a
37	chr7:6690313-6690363	HL-60	blood:	n/a
38	chr7:6693030-6693080	HNPCEpiC	eye:	n/a
39	chr7:6693838-6693888	A549	lung:	n/a
40	chr7:6692445-6692495	Hela-S3	cervix:	n/a
41	chr7:6693838-6693888	AG10803	skin:	n/a
42	chr7:6691949-6691999	K562	blood:	n/a
43	chr7:6693030-6693080	AG10803	skin:	n/a
44	chr7:6691949-6691999	NH-A	brain:	n/a
45	chr7:6691949-6691999	H1-hESC	embryonic stem cell:	embryo
46	chr7:6694373-6694423	IMR90	lung:	fetal
47	chr7:6689218-6689268	HCF	heart:	n/a
48	chr7:6693838-6693888	HCM	heart:	n/a
49	chr7:6690313-6690363	AG09309	skin:	n/a
50	chr7:6692873-6692923	HepG2	liver:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:6680998..6682837-chr7:6692889..6695214,2	MCF-7	breast:
2	chr7:6680149..6683134-chr7:6689202..6690780,2	K562	blood:
3	chr7:6672567..6674181-chr7:6688854..6690680,2	K562	blood:
4	chr7:6674209..6679608-chr7:6682918..6689628,9	K562	blood:
5	chr7:6687023..6688997-chr7:6745010..6747605,2	K562	blood:
6	chr7:6650218..6651893-chr7:6687593..6690254,2	K562	blood:
7	chr7:6674759..6677679-chr7:6692100..6694240,3	MCF-7	breast:
8	chr7:6685863..6688294-chr7:6688920..6690681,2	MCF-7	breast:
9	chr7:6669640..6671625-chr7:6687041..6689974,2	MCF-7	breast:
10	chr7:6683480..6686518-chr7:6689197..6691289,3	MCF-7	breast:
11	chr7:6675427..6681659-chr7:6684293..6688490,10	MCF-7	breast:
12	chr7:6689485..6692014-chr7:6722455..6725146,3	MCF-7	breast:
13	chr7:6682112..6684474-chr7:6686272..6690280,3	MCF-7	breast:
14	chr7:6685863..6688294-chr7:6688920..6690681,2	MCF-7	breast:
15	chr7:6688371..6689911-chr7:6696909..6698726,2	K562	blood:
16	chr7:6676518..6678447-chr7:6694438..6696514,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC073343.1-2	chr7:6694495-6696063	ENSG00000260054.1

No data

Variant related genes	Relation type
ENSG00000260054	TF binding region
ENSG00000260054	CpG island
ENSG00000164631	chromatin interactions
ENSG00000205903	chromatin interactions

Extended variants
information (count: 331 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2140907	chr7:6686601-6686602	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545262665	chr7:6686610-6686611	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs563450271	chr7:6686714-6686715	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs147993073	chr7:6686723-6686724	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs117179192	chr7:6686725-6686726	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs575644980	chr7:6686727-6686728	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs542823021	chr7:6686752-6686753	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs561115590	chr7:6686753-6686754	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs370009550	chr7:6686756-6686757	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs546385369	chr7:6686757-6686758	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs564850822	chr7:6686771-6686772	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs2253480	chr7:6686780-6686781	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs551219047	chr7:6686800-6686801	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs145638044	chr7:6686802-6686803	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs569189518	chr7:6686814-6686815	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs536574787	chr7:6686861-6686862	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs145153853	chr7:6686877-6686878	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs552351213	chr7:6686904-6686905	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs6962510	chr7:6686918-6686919	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs534254982	chr7:6686921-6686922	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs567262205	chr7:6686944-6686945	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs370777386	chr7:6686952-6686953	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs558808965	chr7:6686956-6686957	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs577134766	chr7:6686980-6686981	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs138827984	chr7:6687025-6687026	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs556550013	chr7:6687028-6687029	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs28399923	chr7:6687058-6687059	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs542982561	chr7:6687088-6687089	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs554763938	chr7:6687098-6687099	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs534392982	chr7:6687099-6687100	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs573078092	chr7:6687107-6687108	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs150432944	chr7:6687127-6687128	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs564841920	chr7:6687162-6687163	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs28672377	chr7:6687163-6687164	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs34241573	chr7:6687181-6687182	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs116624371	chr7:6687193-6687194	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs182337736	chr7:6687197-6687198	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs375827620	chr7:6687201-6687202	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs548478168	chr7:6687202-6687203	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs566698832	chr7:6687206-6687207	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs527899026	chr7:6687268-6687269	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs552771618	chr7:6687289-6687290	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs570835676	chr7:6687297-6687298	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs374079619	chr7:6687309-6687310	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs538383150	chr7:6687328-6687329	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs556589723	chr7:6687345-6687346	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs568472242	chr7:6687353-6687354	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs536503018	chr7:6687384-6687385	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs554924493	chr7:6687386-6687387	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs367960525	chr7:6687391-6687392	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Bladder cancer	21909424	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
Autism	20685689	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6678000-6691600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:6678200-6698200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr7:6678400-6691600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:6678400-6691600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr7:6678600-6687800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:6678600-6687800	Strong transcription	Fetal Intestine Large	intestine
7	chr7:6678600-6689600	Strong transcription	Fetal Intestine Small	intestine
8	chr7:6678800-6688600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr7:6678800-6689600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr7:6678800-6691200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr7:6678800-6691400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr7:6679000-6687800	Strong transcription	Fetal Stomach	stomach
13	chr7:6679000-6689200	Strong transcription	Thymus	Thymus
14	chr7:6679000-6689400	Strong transcription	Fetal Thymus	thymus
15	chr7:6679000-6689600	Strong transcription	Cortex derived primary cultured neurospheres	brain
16	chr7:6679000-6690000	Strong transcription	Fetal Brain Female	brain
17	chr7:6679000-6692200	Strong transcription	Primary T cells from cord blood	blood
18	chr7:6679000-6692600	Strong transcription	Primary B cells from peripheral blood	blood
19	chr7:6679000-6695200	Strong transcription	Stomach Smooth Muscle	stomach
20	chr7:6679000-6695400	Strong transcription	Brain Inferior Temporal Lobe	brain
21	chr7:6679200-6690200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr7:6679200-6690200	Strong transcription	Lung	lung
23	chr7:6679200-6690200	Strong transcription	NHLF	lung
24	chr7:6679200-6695400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr7:6679400-6691600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr7:6679400-6691600	Strong transcription	Liver	Liver
27	chr7:6679400-6696400	Strong transcription	Brain Hippocampus Middle	brain
28	chr7:6679400-6703600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr7:6679600-6689200	Strong transcription	Brain Germinal Matrix	brain
30	chr7:6679600-6689400	Strong transcription	Monocytes-CD14+_RO01746	blood
31	chr7:6679600-6689600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr7:6679600-6693200	Strong transcription	Rectal Smooth Muscle	rectum
33	chr7:6679600-6699200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr7:6679800-6687400	Strong transcription	Primary monocytes fromperipheralblood	blood
35	chr7:6679800-6689400	Strong transcription	Primary neutrophils fromperipheralblood	blood
36	chr7:6679800-6689400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr7:6679800-6690600	Strong transcription	Fetal Muscle Leg	muscle
38	chr7:6679800-6695600	Strong transcription	Primary T helper cells fromperipheralblood	blood
39	chr7:6680000-6689000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr7:6680000-6691600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr7:6680000-6692600	Strong transcription	Primary T helper cells PMA-I stimulated	--
42	chr7:6680000-6692600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr7:6680000-6695200	Strong transcription	Duodenum Mucosa	Duodenum
44	chr7:6680200-6686800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
45	chr7:6680200-6690200	Strong transcription	Placenta	Placenta
46	chr7:6680200-6690800	Strong transcription	Esophagus	oesophagus
47	chr7:6680200-6691600	Strong transcription	Colonic Mucosa	Colon
48	chr7:6680200-6691800	Weak transcription	Fetal Brain Male	brain
49	chr7:6680400-6688200	Strong transcription	Pancreas	Pancrea
50	chr7:6680400-6691000	Strong transcription	Sigmoid Colon	Sigmoid Colon

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