Variant report

Variant	nsv830905
Chromosome Location	chr7:11793513-11941594
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:869)
CpG islands
(count:733)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:869 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr7:11824302-11824793	A549	lung:	n/a	n/a
2	ATF3	chr7:11825723-11826201	A549	lung:	n/a	n/a
3	ATF3	chr7:11824198-11824878	A549	lung:	n/a	n/a
4	BACH1	chr7:11847468-11847585	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr7:11793826-11794047	GM12878	blood:	n/a	n/a
6	BCL3	chr7:11824091-11825180	A549	lung:	n/a	n/a
7	BCL3	chr7:11824203-11825161	A549	lung:	n/a	n/a
8	BCL3	chr7:11871735-11872344	A549	lung:	n/a	chr7:11871832-11871845 chr7:11871797-11871810
9	BCL3	chr7:11825673-11826332	A549	lung:	n/a	chr7:11825696-11825705
10	BCL3	chr7:11825494-11826405	A549	lung:	n/a	chr7:11825696-11825705 chr7:11825577-11825586
11	BRCA1	chr7:11872030-11872097	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr7:11872708-11872806	GM12878	blood:	n/a	n/a
13	CCNT2	chr7:11840944-11841113	K562	blood:	n/a	n/a
14	CEBPB	chr7:11870201-11870502	H1-hESC	embryonic stem cell:	n/a	chr7:11870316-11870327
15	CEBPB	chr7:11815226-11815593	A549	lung:	n/a	chr7:11815386-11815397
16	CEBPB	chr7:11841232-11841562	A549	lung:	n/a	n/a
17	CEBPB	chr7:11815197-11815546	A549	lung:	n/a	chr7:11815386-11815397
18	CEBPB	chr7:11825827-11826295	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr7:11887894-11888135	HepG2	liver:	n/a	chr7:11887971-11887982 chr7:11888100-11888113
20	CEBPB	chr7:11799176-11799419	A549	lung:	n/a	n/a
21	CEBPB	chr7:11841230-11841543	HepG2	liver:	n/a	n/a
22	CEBPB	chr7:11837927-11838120	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr7:11870223-11870404	HepG2	liver:	n/a	chr7:11870316-11870327
24	CEBPB	chr7:11800004-11800338	A549	lung:	n/a	n/a
25	CEBPB	chr7:11872647-11872885	A549	lung:	n/a	n/a
26	CEBPB	chr7:11825736-11826324	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr7:11825756-11826243	A549	lung:	n/a	n/a
28	CEBPB	chr7:11815101-11815624	A549	lung:	n/a	chr7:11815386-11815397
29	CEBPB	chr7:11815233-11815526	HepG2	liver:	n/a	chr7:11815386-11815397
30	CEBPB	chr7:11799997-11800389	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr7:11837911-11838111	A549	lung:	n/a	n/a
32	CEBPB	chr7:11886003-11886186	K562	blood:	n/a	chr7:11886090-11886107
33	CEBPB	chr7:11798100-11798840	A549	lung:	n/a	n/a
34	CEBPB	chr7:11815259-11815421	H1-hESC	embryonic stem cell:	n/a	chr7:11815386-11815397
35	CEBPB	chr7:11824316-11825017	A549	lung:	n/a	n/a
36	CEBPB	chr7:11825667-11826387	A549	lung:	n/a	n/a
37	CEBPB	chr7:11825886-11826179	MCF-7	breast:	n/a	n/a
38	CEBPB	chr7:11798081-11798599	A549	lung:	n/a	n/a
39	CEBPB	chr7:11824785-11824789	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr7:11815223-11815541	IMR90	lung:	n/a	chr7:11815386-11815397
41	CEBPB	chr7:11812246-11812512	A549	lung:	n/a	n/a
42	CEBPB	chr7:11799871-11800447	A549	lung:	n/a	n/a
43	CEBPB	chr7:11886022-11886252	A549	lung:	n/a	chr7:11886090-11886107
44	CEBPB	chr7:11800021-11800345	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPB	chr7:11885995-11886338	H1-hESC	embryonic stem cell:	n/a	chr7:11886090-11886107
46	CEBPB	chr7:11855870-11856102	A549	lung:	n/a	chr7:11855946-11855959
47	CEBPB	chr7:11825894-11826159	MCF-7	breast:	n/a	n/a
48	CEBPB	chr7:11799964-11800365	A549	lung:	n/a	n/a
49	CEBPB	chr7:11824245-11824995	A549	lung:	n/a	n/a
50	CEBPB	chr7:11938973-11939285	Hela-S3	cervix:	n/a	chr7:11939119-11939132 chr7:11939119-11939130 chr7:11939119-11939130

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:11856910-11856960	PFSK-1	brain:	n/a
2	chr7:11856910-11856960	PFSK-1	brain:	n/a
3	chr7:11871837-11871887	HMEC	breast:	n/a
4	chr7:11860398-11860448	IMR90	lung:	fetal
5	chr7:11871843-11871893	NH-A	brain:	n/a
6	chr7:11872050-11872100	AG09319	gingival:	n/a
7	chr7:11871843-11871893	SAEC	small airway:	n/a
8	chr7:11886927-11886977	PrEC	prostate:	n/a
9	chr7:11871535-11871585	A549	lung:	n/a
10	chr7:11872009-11872059	NHBE	bronchial:	n/a
11	chr7:11871906-11871956	HCT-116	colon:	n/a
12	chr7:11871843-11871893	GM19239	blood:	n/a
13	chr7:11871837-11871887	RPTEC	kidney:	n/a
14	chr7:11872073-11872123	HepG2	liver:	n/a
15	chr7:11856910-11856960	CMK	blood:	n/a
16	chr7:11871843-11871893	ECC-1	luminal epithelium:	n/a
17	chr7:11872073-11872123	HCM	heart:	n/a
18	chr7:11871906-11871956	HepG2	liver:	n/a
19	chr7:11871690-11871740	HMEC	breast:	n/a
20	chr7:11872009-11872059	ovcar-3	ovarian:	n/a
21	chr7:11871535-11871585	Jurkat	blood:	n/a
22	chr7:11860398-11860448	K562	blood:	n/a
23	chr7:11886927-11886977	MCF-7	breast:	n/a
24	chr7:11872059-11872109	HRCEpiC	kidney:	n/a
25	chr7:11872059-11872109	K562	blood:	n/a
26	chr7:11872050-11872100	A549	lung:	n/a
27	chr7:11872009-11872059	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:11871690-11871740	HCM	heart:	n/a
29	chr7:11886927-11886977	HCPEpiC	choroid plexus:	n/a
30	chr7:11871690-11871740	AG04449	skin:	fetal
31	chr7:11871843-11871893	AG10803	skin:	n/a
32	chr7:11886927-11886977	NHBE	bronchial:	n/a
33	chr7:11871837-11871887	HNPCEpiC	eye:	n/a
34	chr7:11886927-11886977	PFSK-1	brain:	n/a
35	chr7:11871690-11871740	PFSK-1	brain:	n/a
36	chr7:11871535-11871585	HCM	heart:	n/a
37	chr7:11871535-11871585	GM12892	blood:	n/a
38	chr7:11871690-11871740	H1-hESC	embryonic stem cell:	embryo
39	chr7:11872059-11872109	HCT-116	colon:	n/a
40	chr7:11872073-11872123	HRPEpiC	eye:	n/a
41	chr7:11871535-11871585	PANC-1	pancreas:	n/a
42	chr7:11856910-11856960	AG10803	skin:	n/a
43	chr7:11886927-11886977	GM12891	blood:	n/a
44	chr7:11871837-11871887	HCM	heart:	n/a
45	chr7:11886927-11886977	HAEpiC	amniotic membrane:	n/a
46	chr7:11871843-11871893	HEK293	kidney:	embryo
47	chr7:11872050-11872100	HRCEpiC	kidney:	n/a
48	chr7:11886927-11886977	AG09319	gingival:	n/a
49	chr7:11871843-11871893	HAEpiC	amniotic membrane:	n/a
50	chr7:11871837-11871887	CMK	blood:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:11825792..11827452-chr7:12250690..12252640,2	MCF-7	breast:
2	chr17:57920770..57923086-chr7:11840317..11842136,2	MCF-7	breast:
3	chr7:11869044..11871618-chr7:11911961..11914333,2	K562	blood:
4	chr7:11869044..11871618-chr7:11911961..11914333,2	K562	blood:
5	chr7:11605955..11606651-chr7:11870687..11871656,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000235920	TF binding region
THSD7A	TF binding region
ENSG00000235920	CpG island
THSD7A	CpG island
ENSG00000106460	chromatin interactions

Extended variants
information (count: 4987 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:4987 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188120140	chr7:11793600-11793601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs372956377	chr7:11793622-11793623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181020936	chr7:11793628-11793629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561767280	chr7:11793636-11793637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561523793	chr7:11793648-11793649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs34691522	chr7:11793685-11793686	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs527278870	chr7:11793691-11793692	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs530277153	chr7:11793699-11793700	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs148349518	chr7:11793736-11793737	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs78107658	chr7:11793746-11793747	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs550411888	chr7:11793779-11793780	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs570110898	chr7:11793797-11793798	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs187126832	chr7:11793809-11793810	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs551653692	chr7:11793860-11793861	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs145682183	chr7:11793866-11793867	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs566107179	chr7:11793903-11793904	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs534685732	chr7:11793906-11793907	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs75192947	chr7:11793916-11793917	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs564111560	chr7:11793923-11793924	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs138242847	chr7:11794045-11794046	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs117718396	chr7:11794049-11794050	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs192143783	chr7:11794051-11794052	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs142785750	chr7:11794146-11794147	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs117888400	chr7:11794153-11794154	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs150604577	chr7:11794181-11794182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs115654728	chr7:11794221-11794222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs6460840	chr7:11794239-11794240	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs574844705	chr7:11794257-11794258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs139623761	chr7:11794366-11794367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs536089835	chr7:11794372-11794373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs533068886	chr7:11794383-11794384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs549855587	chr7:11794394-11794395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs549861203	chr7:11794450-11794451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183965766	chr7:11794491-11794492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149323501	chr7:11794512-11794513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs144570459	chr7:11794530-11794531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368365123	chr7:11794541-11794542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs372589118	chr7:11794555-11794556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs569619873	chr7:11794563-11794564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535517430	chr7:11794599-11794600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs115224488	chr7:11794602-11794603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs549242282	chr7:11794618-11794619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs115903934	chr7:11794644-11794645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs551379133	chr7:11794662-11794663	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs386710339	chr7:11794676-11794677	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs11761153	chr7:11794677-11794678	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs535831404	chr7:11794701-11794702	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs576217503	chr7:11794728-11794729	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs375141189	chr7:11794759-11794760	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs139649405	chr7:11794763-11794764	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Melanoma	18172304	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
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Autism	22495309	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD
Melanoma	20877625	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Rett syndrome	21593744	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:696 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:11791600-11795000	Weak transcription	Placenta	Placenta
2	chr7:11792600-11795000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:11792600-11795000	Enhancers	A549	lung
4	chr7:11792800-11794200	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr7:11794200-11794800	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr7:11794800-11796400	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr7:11795000-11795400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:11795000-11795400	Enhancers	Placenta	Placenta
9	chr7:11795000-11795400	Flanking Active TSS	A549	lung
10	chr7:11795400-11795600	Active TSS	A549	lung
11	chr7:11795400-11798000	Weak transcription	Placenta	Placenta
12	chr7:11795600-11795800	Flanking Active TSS	A549	lung
13	chr7:11795800-11796800	Active TSS	A549	lung
14	chr7:11796400-11800000	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr7:11796800-11797000	Flanking Active TSS	A549	lung
16	chr7:11797000-11797200	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr7:11797000-11798000	Enhancers	A549	lung
18	chr7:11797600-11799200	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr7:11798000-11798400	Flanking Active TSS	A549	lung
20	chr7:11798000-11798600	Enhancers	Placenta	Placenta
21	chr7:11798400-11798800	Active TSS	A549	lung
22	chr7:11798600-11803000	Weak transcription	Placenta	Placenta
23	chr7:11798800-11799600	Weak transcription	A549	lung
24	chr7:11799200-11800400	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr7:11799600-11799800	Flanking Active TSS	A549	lung
26	chr7:11799800-11800200	Active TSS	A549	lung
27	chr7:11800000-11800400	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr7:11800000-11800400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr7:11800200-11800800	Weak transcription	A549	lung
30	chr7:11800400-11811200	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr7:11800800-11801600	Enhancers	A549	lung
32	chr7:11801600-11802600	Weak transcription	A549	lung
33	chr7:11802600-11803000	Enhancers	A549	lung
34	chr7:11803000-11805800	Weak transcription	A549	lung
35	chr7:11805000-11805200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:11805800-11806000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr7:11805800-11807800	Enhancers	A549	lung
38	chr7:11806600-11807000	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr7:11806600-11807200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr7:11807800-11809600	Weak transcription	A549	lung
41	chr7:11809600-11810400	Enhancers	A549	lung
42	chr7:11810400-11812200	Weak transcription	A549	lung
43	chr7:11811200-11811800	Strong transcription	Cortex derived primary cultured neurospheres	brain
44	chr7:11811400-11811600	Enhancers	Esophagus	oesophagus
45	chr7:11811800-11825800	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr7:11812200-11812800	ZNF genes & repeats	A549	lung
47	chr7:11812800-11813400	Weak transcription	A549	lung
48	chr7:11813400-11814800	Enhancers	A549	lung
49	chr7:11814800-11815000	Flanking Active TSS	A549	lung
50	chr7:11815000-11815200	Active TSS	A549	lung

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