Variant report

Variant	nsv887965
Chromosome Location	chr7:38706384-38793243
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:714)
CpG islands
(count:977)
Chromatin interactive
region (count:25)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:714 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:38788004-38788218	HepG2	liver:	n/a	n/a
2	ATF1	chr7:38749724-38749827	K562	blood:	n/a	n/a
3	BHLHE40	chr7:38775167-38775236	K562	blood:	n/a	n/a
4	BHLHE40	chr7:38711722-38712119	GM12878	blood:	n/a	chr7:38711878-38711894
5	CEBPB	chr7:38719188-38719408	IMR90	lung:	n/a	n/a
6	CEBPB	chr7:38717572-38717848	K562	blood:	n/a	chr7:38717729-38717740
7	CEBPB	chr7:38713387-38713665	A549	lung:	n/a	n/a
8	CEBPB	chr7:38722426-38722731	H1-hESC	embryonic stem cell:	n/a	chr7:38722580-38722591
9	CEBPB	chr7:38792095-38792410	IMR90	lung:	n/a	chr7:38792233-38792244
10	CEBPB	chr7:38730362-38730566	A549	lung:	n/a	chr7:38730398-38730411
11	CEBPB	chr7:38739106-38739422	IMR90	lung:	n/a	n/a
12	CEBPB	chr7:38742681-38742995	MCF-7	breast:	n/a	n/a
13	CEBPB	chr7:38722422-38722753	IMR90	lung:	n/a	chr7:38722580-38722591
14	CEBPB	chr7:38730283-38730493	HepG2	liver:	n/a	chr7:38730398-38730411
15	CEBPB	chr7:38717637-38717882	A549	lung:	n/a	chr7:38717729-38717740
16	CEBPB	chr7:38742606-38743041	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:38792082-38792385	A549	lung:	n/a	chr7:38792233-38792244
18	CEBPB	chr7:38726597-38726851	A549	lung:	n/a	chr7:38726698-38726709
19	CEBPB	chr7:38717567-38717907	K562	blood:	n/a	chr7:38717729-38717740
20	CEBPB	chr7:38713424-38713710	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr7:38742654-38742836	K562	blood:	n/a	n/a
22	CEBPB	chr7:38726585-38726792	HepG2	liver:	n/a	chr7:38726698-38726709
23	CEBPB	chr7:38713322-38713797	IMR90	lung:	n/a	n/a
24	CEBPB	chr7:38722437-38722767	HepG2	liver:	n/a	chr7:38722580-38722591
25	CEBPB	chr7:38730291-38730496	IMR90	lung:	n/a	chr7:38730398-38730411
26	CEBPB	chr7:38709659-38709914	HepG2	liver:	n/a	chr7:38709863-38709876 chr7:38709743-38709754
27	CEBPB	chr7:38791003-38791334	IMR90	lung:	n/a	n/a
28	CEBPB	chr7:38792076-38792410	HepG2	liver:	n/a	chr7:38792233-38792244
29	CEBPB	chr7:38776518-38776642	A549	lung:	n/a	chr7:38776619-38776630 chr7:38776619-38776630
30	CEBPB	chr7:38784371-38784769	Hela-S3	cervix:	n/a	chr7:38784562-38784575 chr7:38784562-38784573 chr7:38784563-38784574
31	CEBPB	chr7:38784403-38784762	ECC-1	luminal epithelium:	n/a	chr7:38784562-38784575 chr7:38784562-38784573 chr7:38784563-38784574
32	CEBPB	chr7:38742577-38742951	A549	lung:	n/a	n/a
33	CEBPB	chr7:38784416-38784695	HepG2	liver:	n/a	chr7:38784562-38784575 chr7:38784562-38784573 chr7:38784563-38784574
34	CEBPB	chr7:38747288-38747614	HepG2	liver:	n/a	chr7:38747459-38747470
35	CEBPB	chr7:38784421-38784756	ECC-1	luminal epithelium:	n/a	chr7:38784562-38784575 chr7:38784562-38784573 chr7:38784563-38784574
36	CEBPB	chr7:38792183-38792344	H1-hESC	embryonic stem cell:	n/a	chr7:38792233-38792244
37	CEBPB	chr7:38784376-38784760	IMR90	lung:	n/a	chr7:38784562-38784575 chr7:38784562-38784573 chr7:38784563-38784574
38	CEBPB	chr7:38722470-38722710	MCF-7	breast:	n/a	chr7:38722580-38722591
39	CEBPB	chr7:38784442-38784717	K562	blood:	n/a	chr7:38784562-38784575 chr7:38784562-38784573 chr7:38784563-38784574
40	CEBPB	chr7:38747303-38747570	A549	lung:	n/a	chr7:38747459-38747470
41	CEBPB	chr7:38717621-38717892	HepG2	liver:	n/a	chr7:38717729-38717740
42	CEBPB	chr7:38757435-38757673	K562	blood:	n/a	n/a
43	CEBPB	chr7:38747327-38747597	K562	blood:	n/a	chr7:38747459-38747470
44	CEBPB	chr7:38792128-38792331	K562	blood:	n/a	chr7:38792233-38792244
45	CEBPB	chr7:38747324-38747603	IMR90	lung:	n/a	chr7:38747459-38747470
46	CEBPB	chr7:38716942-38716979	A549	lung:	n/a	n/a
47	CEBPB	chr7:38722394-38722724	K562	blood:	n/a	chr7:38722580-38722591
48	CHD2	chr7:38793027-38793191	K562	blood:	n/a	n/a
49	CTCF	chr7:38756160-38756310	GM12873	blood:	n/a	n/a
50	CTCF	chr7:38756060-38756210	WERI-Rb-1	eye:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38710069-38710119	HEK293	kidney:	embryo
2	chr7:38710069-38710119	HEK293	kidney:	embryo
3	chr7:38726323-38726373	NH-A	brain:	n/a
4	chr7:38720626-38720676	HRPEpiC	eye:	n/a
5	chr7:38710069-38710119	HCT-116	colon:	n/a
6	chr7:38725962-38726012	HCM	heart:	n/a
7	chr7:38743230-38743280	PrEC	prostate:	n/a
8	chr7:38726323-38726373	HRCEpiC	kidney:	n/a
9	chr7:38764256-38764306	Hela-S3	cervix:	n/a
10	chr7:38725419-38725469	GM06990	blood:	n/a
11	chr7:38739258-38739308	IMR90	lung:	fetal
12	chr7:38767436-38767486	ovcar-3	ovarian:	n/a
13	chr7:38767436-38767486	HEEpiC	esophagus:	n/a
14	chr7:38743230-38743280	BE2_C	brain:	n/a
15	chr7:38725419-38725469	NHBE	bronchial:	n/a
16	chr7:38726758-38726808	HCT-116	colon:	n/a
17	chr7:38725419-38725469	Hepatocyte	liver:	n/a
18	chr7:38767436-38767486	GM06990	blood:	n/a
19	chr7:38726897-38726947	AoSMC	blood vessel:	n/a
20	chr7:38777574-38777624	CMK	blood:	n/a
21	chr7:38726897-38726947	PrEC	prostate:	n/a
22	chr7:38791870-38791920	GM12891	blood:	n/a
23	chr7:38726323-38726373	HIPEpiC	eye:	n/a
24	chr7:38720626-38720676	MCF-7	breast:	n/a
25	chr7:38743230-38743280	MCF-7	breast:	n/a
26	chr7:38726323-38726373	HEK293	kidney:	embryo
27	chr7:38743230-38743280	T-47D	breast:	n/a
28	chr7:38727894-38727944	HPAEpiC	pulmonary alveolar:	n/a
29	chr7:38764256-38764306	HepG2	liver:	n/a
30	chr7:38791870-38791920	HCF	heart:	n/a
31	chr7:38725630-38725680	SKMC	muscle:	n/a
32	chr7:38728135-38728185	Caco-2	colon:	n/a
33	chr7:38726897-38726947	BJ	skin:	n/a
34	chr7:38725419-38725469	BE2_C	brain:	n/a
35	chr7:38726758-38726808	GM12891	blood:	n/a
36	chr7:38725419-38725469	AG10803	skin:	n/a
37	chr7:38767436-38767486	AG09319	gingival:	n/a
38	chr7:38725962-38726012	HIPEpiC	eye:	n/a
39	chr7:38739258-38739308	HRE	kidney:	n/a
40	chr7:38710069-38710119	Hela-S3	cervix:	n/a
41	chr7:38725419-38725469	NB4	blood:	n/a
42	chr7:38728135-38728185	K562	blood:	n/a
43	chr7:38727894-38727944	NT2-D1	testis:	n/a
44	chr7:38725962-38726012	HAEpiC	amniotic membrane:	n/a
45	chr7:38725962-38726012	GM06990	blood:	n/a
46	chr7:38791870-38791920	AG09309	skin:	n/a
47	chr7:38725630-38725680	A549	lung:	n/a
48	chr7:38725962-38726012	HCT-116	colon:	n/a
49	chr7:38764256-38764306	BJ	skin:	n/a
50	chr7:38727894-38727944	HRE	kidney:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:38787332..38789165-chr7:38790853..38793676,2	K562	blood:
2	chr7:38737792..38739807-chr7:38743748..38746475,2	K562	blood:
3	chr7:38787918..38790102-chr7:38792675..38794796,2	MCF-7	breast:
4	chr7:38774892..38777072-chr7:39005282..39007402,2	K562	blood:
5	chr7:38779167..38781371-chr7:38782858..38784712,2	MCF-7	breast:
6	chr7:38473622..38474218-chr7:38787900..38788567,2	MCF-7	breast:
7	chr7:38744831..38747326-chr7:38766481..38768901,2	K562	blood:
8	chr7:38790727..38792284-chr7:38793430..38795338,2	MCF-7	breast:
9	chr7:38777448..38781271-chr7:38790893..38794034,3	K562	blood:
10	chr7:38772482..38774606-chr7:38774612..38777168,2	K562	blood:
11	chr7:38787332..38789165-chr7:38790853..38793676,2	K562	blood:
12	chr7:38772482..38774606-chr7:38774612..38777168,2	K562	blood:
13	chr7:38775769..38777422-chr7:38778877..38780548,2	MCF-7	breast:
14	chr7:38777448..38781271-chr7:38790893..38794034,3	K562	blood:
15	chr7:38779167..38781371-chr7:38782858..38784712,2	MCF-7	breast:
16	chr7:38737792..38739807-chr7:38743748..38746475,2	K562	blood:
17	chr7:38740549..38744081-chr7:38747124..38750067,4	K562	blood:
18	chr7:38787918..38790102-chr7:38792675..38794796,2	MCF-7	breast:
19	chr7:38740549..38744081-chr7:38747124..38750067,4	K562	blood:
20	chr7:38767860..38770728-chr7:38772914..38774538,2	MCF-7	breast:
21	chr7:38776633..38779094-chr7:38783053..38785057,2	K562	blood:
22	chr7:38714008..38715594-chr7:38725916..38727906,2	K562	blood:
23	chr7:38767860..38770728-chr7:38772914..38774538,2	MCF-7	breast:
24	chr7:38776633..38779094-chr7:38783053..38785057,2	K562	blood:
25	chr7:38775769..38777422-chr7:38778877..38780548,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POU6F2-3	chr7:38740269-38740963	NONHSAT120189
2	lnc-POU6F2-3	chr7:38741067-38741258	NONHSAT120189
3	lnc-POU6F2-2	chr7:38750901-38751632	NONHSAT120190

No data

Variant related genes	Relation type
FAM183B	TF binding region
VPS41	TF binding region
FAM183B	CpG island
VPS41	CpG island
ENSG00000006715	chromatin interactions
ENSG00000164556	chromatin interactions

Extended variants
information (count: 3077 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:3077 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10279772	chr7:38706384-38706385	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs57365048	chr7:38706589-38706590	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs561032794	chr7:38706590-38706591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529695149	chr7:38706620-38706621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537795628	chr7:38706663-38706664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs76984252	chr7:38706732-38706733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532467811	chr7:38706736-38706737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181565754	chr7:38706742-38706743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569082195	chr7:38706814-38706815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs10280089	chr7:38706817-38706818	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs57353808	chr7:38706831-38706832	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs531502629	chr7:38706855-38706856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148886366	chr7:38706881-38706882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536279910	chr7:38706959-38706960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552972204	chr7:38706982-38706983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs28393327	chr7:38707058-38707059	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs61332683	chr7:38707067-38707068	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs558781193	chr7:38707074-38707075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575797828	chr7:38707075-38707076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183882748	chr7:38707197-38707198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544785715	chr7:38707209-38707210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560856216	chr7:38707254-38707255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368101611	chr7:38707312-38707313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548203101	chr7:38707333-38707334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs140617514	chr7:38707339-38707340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539923640	chr7:38707364-38707365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560207668	chr7:38707377-38707378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145616089	chr7:38707395-38707396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189910181	chr7:38707399-38707400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181416024	chr7:38707448-38707449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531439942	chr7:38707481-38707482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200959119	chr7:38707488-38707489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548343237	chr7:38707499-38707500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201775043	chr7:38707506-38707507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568132492	chr7:38707516-38707517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs199597395	chr7:38707518-38707519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200481405	chr7:38707528-38707529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536765864	chr7:38707536-38707537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201671675	chr7:38707560-38707561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546647594	chr7:38707579-38707580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371979629	chr7:38707612-38707613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542693120	chr7:38707633-38707634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566529139	chr7:38707637-38707638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530528912	chr7:38707727-38707728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555928893	chr7:38707734-38707735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575987333	chr7:38707735-38707736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575882006	chr7:38707741-38707742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148794955	chr7:38707768-38707769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564404546	chr7:38707780-38707781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574902546	chr7:38707782-38707783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
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
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Sezary syndrome	18413736	CNVD
Gastric cancer	24379144	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1166 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38696000-38726000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:38708800-38710400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr7:38708800-38710800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr7:38709800-38710400	Enhancers	Adipose Nuclei	Adipose
5	chr7:38710400-38711800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:38710800-38711200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:38710800-38712600	Enhancers	Primary B cells from peripheral blood	blood
8	chr7:38711200-38712600	Enhancers	Primary B cells from cord blood	blood
9	chr7:38711200-38715800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr7:38711400-38712200	Enhancers	Spleen	Spleen
11	chr7:38711600-38712400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr7:38711600-38714600	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr7:38711600-38714800	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr7:38711800-38712400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:38712200-38712600	Enhancers	NHDF-Ad	bronchial
16	chr7:38712400-38713000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr7:38712600-38713000	Weak transcription	NHDF-Ad	bronchial
18	chr7:38712600-38713600	Weak transcription	Primary B cells from cord blood	blood
19	chr7:38713000-38715600	Enhancers	NHDF-Ad	bronchial
20	chr7:38713000-38715800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr7:38713200-38714000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr7:38713200-38714000	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr7:38713200-38714000	Enhancers	HUVEC	blood vessel
24	chr7:38713200-38714400	Enhancers	Muscle Satellite Cultured Cells	--
25	chr7:38713200-38714600	Enhancers	HMEC	breast
26	chr7:38713400-38714000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr7:38713400-38714800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr7:38713600-38713800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr7:38713600-38714000	Enhancers	Fetal Muscle Leg	muscle
30	chr7:38713800-38714000	Enhancers	Primary B cells from cord blood	blood
31	chr7:38714000-38714400	Enhancers	Fetal Brain Female	brain
32	chr7:38714000-38715800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr7:38714000-38719000	Weak transcription	HUVEC	blood vessel
34	chr7:38714000-38721800	Weak transcription	Fetal Muscle Leg	muscle
35	chr7:38714400-38714800	Weak transcription	Fetal Brain Female	brain
36	chr7:38714400-38715400	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr7:38714600-38715600	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr7:38714600-38715600	Enhancers	Ovary	ovary
39	chr7:38714600-38717200	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr7:38714800-38715400	Enhancers	Fetal Brain Female	brain
41	chr7:38714800-38717400	Weak transcription	Primary monocytes fromperipheralblood	blood
42	chr7:38715000-38715400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr7:38715000-38715400	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr7:38715000-38715600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr7:38715200-38715400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr7:38715200-38715600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr7:38715200-38715600	Enhancers	Fetal Brain Male	brain
48	chr7:38715800-38716800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr7:38715800-38719000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr7:38716800-38717600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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