Variant report

Variant	nsv887645
Chromosome Location	chr7:13132400-13220153
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:711)
CpG islands
(count:123)
Chromatin interactive
region (count:39)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:711 , 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	chr7:13138761-13139142	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:13143806-13144072	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:13156776-13157108	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:13143855-13144055	K562	blood:	n/a	n/a
5	ARID3A	chr7:13176170-13176171	K562	blood:	n/a	n/a
6	ARID3A	chr7:13156744-13157084	K562	blood:	n/a	n/a
7	ATF1	chr7:13172051-13172233	K562	blood:	n/a	n/a
8	ATF1	chr7:13187153-13187258	K562	blood:	n/a	n/a
9	ATF1	chr7:13158387-13158436	K562	blood:	n/a	n/a
10	ATF1	chr7:13143829-13144112	K562	blood:	n/a	n/a
11	ATF3	chr7:13191565-13191942	K562	blood:	n/a	n/a
12	BACH1	chr7:13219156-13219263	K562	blood:	n/a	n/a
13	BATF	chr7:13138876-13139164	GM12878	blood:	n/a	chr7:13139007-13139018
14	BATF	chr7:13138851-13139153	GM12878	blood:	n/a	chr7:13139007-13139018
15	BHLHE40	chr7:13138780-13139161	HepG2	liver:	n/a	n/a
16	BHLHE40	chr7:13210877-13210897	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:13206129-13206138	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:13138027-13138202	K562	blood:	n/a	n/a
19	CBX3	chr7:13175950-13176286	K562	blood:	n/a	n/a
20	CBX3	chr7:13164235-13164595	K562	blood:	n/a	n/a
21	CBX3	chr7:13175978-13176252	K562	blood:	n/a	n/a
22	CBX3	chr7:13149470-13149761	K562	blood:	n/a	n/a
23	CBX3	chr7:13207821-13208141	K562	blood:	n/a	n/a
24	CCNT2	chr7:13215469-13215744	K562	blood:	n/a	n/a
25	CEBPB	chr7:13179118-13179413	HepG2	liver:	n/a	chr7:13179288-13179299
26	CEBPB	chr7:13143857-13144090	K562	blood:	n/a	n/a
27	CEBPB	chr7:13154798-13155176	IMR90	lung:	n/a	n/a
28	CEBPB	chr7:13154823-13155166	K562	blood:	n/a	n/a
29	CEBPB	chr7:13195669-13196034	MCF-7	breast:	n/a	n/a
30	CEBPB	chr7:13144858-13145220	HepG2	liver:	n/a	chr7:13145038-13145051 chr7:13145038-13145049 chr7:13145040-13145051
31	CEBPB	chr7:13147374-13147981	A549	lung:	n/a	chr7:13147889-13147897
32	CEBPB	chr7:13190054-13190280	A549	lung:	n/a	chr7:13190158-13190171
33	CEBPB	chr7:13154568-13155190	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr7:13194534-13194554	A549	lung:	n/a	n/a
35	CEBPB	chr7:13147629-13147716	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr7:13219738-13220007	HepG2	liver:	n/a	chr7:13219909-13219920 chr7:13219909-13219920 chr7:13219907-13219918 chr7:13219907-13219920
37	CEBPB	chr7:13154829-13155112	K562	blood:	n/a	n/a
38	CEBPB	chr7:13179132-13179455	IMR90	lung:	n/a	chr7:13179288-13179299
39	CEBPB	chr7:13138823-13139128	HepG2	liver:	n/a	n/a
40	CEBPB	chr7:13179227-13179427	K562	blood:	n/a	chr7:13179288-13179299
41	CEBPB	chr7:13147885-13147964	K562	blood:	n/a	chr7:13147889-13147897
42	CEBPB	chr7:13144953-13145094	K562	blood:	n/a	chr7:13145038-13145051 chr7:13145038-13145049 chr7:13145040-13145051
43	CEBPB	chr7:13147632-13147985	HepG2	liver:	n/a	chr7:13147889-13147897
44	CEBPB	chr7:13131816-13132430	IMR90	lung:	n/a	n/a
45	CEBPB	chr7:13195701-13195965	K562	blood:	n/a	n/a
46	CEBPB	chr7:13154797-13155156	K562	blood:	n/a	n/a
47	CEBPB	chr7:13191743-13191904	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr7:13200212-13200322	K562	blood:	n/a	n/a
49	CEBPB	chr7:13144926-13145120	HepG2	liver:	n/a	chr7:13145038-13145051 chr7:13145038-13145049 chr7:13145040-13145051
50	CEBPB	chr7:13136917-13137388	K562	blood:	n/a	chr7:13136945-13136958 chr7:13137277-13137288

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:13155344-13155394	IMR90	lung:	fetal
2	chr7:13155344-13155394	IMR90	lung:	fetal
3	chr7:13141735-13141785	HCPEpiC	choroid plexus:	n/a
4	chr7:13141735-13141785	GM12891	blood:	n/a
5	chr7:13141735-13141785	HIPEpiC	eye:	n/a
6	chr7:13141735-13141785	GM12892	blood:	n/a
7	chr7:13155344-13155394	NHBE	bronchial:	n/a
8	chr7:13141735-13141785	AG09319	gingival:	n/a
9	chr7:13155344-13155394	HAEpiC	amniotic membrane:	n/a
10	chr7:13155344-13155394	HepG2	liver:	n/a
11	chr7:13141735-13141785	CMK	blood:	n/a
12	chr7:13155344-13155394	GM12892	blood:	n/a
13	chr7:13155344-13155394	PANC-1	pancreas:	n/a
14	chr7:13141735-13141785	HPAEpiC	pulmonary alveolar:	n/a
15	chr7:13155344-13155394	HEEpiC	esophagus:	n/a
16	chr7:13141735-13141785	AG09309	skin:	n/a
17	chr7:13155344-13155394	HRE	kidney:	n/a
18	chr7:13141735-13141785	A549	lung:	n/a
19	chr7:13141735-13141785	PrEC	prostate:	n/a
20	chr7:13155344-13155394	Jurkat	blood:	n/a
21	chr7:13141735-13141785	SK-N-SH	brain:	n/a
22	chr7:13155344-13155394	LNCaP	prostate:	n/a
23	chr7:13155344-13155394	HCPEpiC	choroid plexus:	n/a
24	chr7:13141735-13141785	HRCEpiC	kidney:	n/a
25	chr7:13141735-13141785	NHBE	bronchial:	n/a
26	chr7:13141735-13141785	HMEC	breast:	n/a
27	chr7:13155344-13155394	HCF	heart:	n/a
28	chr7:13155344-13155394	HCT-116	colon:	n/a
29	chr7:13141735-13141785	AoSMC	blood vessel:	n/a
30	chr7:13141735-13141785	HNPCEpiC	eye:	n/a
31	chr7:13141735-13141785	U87	brain:	n/a
32	chr7:13155344-13155394	HNPCEpiC	eye:	n/a
33	chr7:13141735-13141785	Hepatocyte	liver:	n/a
34	chr7:13155344-13155394	AG04449	skin:	fetal
35	chr7:13155344-13155394	ovcar-3	ovarian:	n/a
36	chr7:13141735-13141785	RPTEC	kidney:	n/a
37	chr7:13141735-13141785	BJ	skin:	n/a
38	chr7:13141735-13141785	HepG2	liver:	n/a
39	chr7:13141735-13141785	Jurkat	blood:	n/a
40	chr7:13155344-13155394	HL-60	blood:	n/a
41	chr7:13155344-13155394	GM19239	blood:	n/a
42	chr7:13141735-13141785	HRPEpiC	eye:	n/a
43	chr7:13155344-13155394	SK-N-MC	brain:	n/a
44	chr7:13155344-13155394	AG10803	skin:	n/a
45	chr7:13141735-13141785	PANC-1	pancreas:	n/a
46	chr7:13141735-13141785	HUVEC	blood vessel:	n/a
47	chr7:13155344-13155394	AG09319	gingival:	n/a
48	chr7:13141735-13141785	GM06990	blood:	n/a
49	chr7:13141735-13141785	GM19239	blood:	n/a
50	chr7:13155344-13155394	BJ	skin:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:52401294..52403111-chr7:13210219..13212096,2	MCF-7	breast:
2	chr7:13130850..13133041-chr7:13136588..13139070,3	K562	blood:
3	chr7:12722672..12723612-chr7:13218588..13219274,2	MCF-7	breast:
4	chr7:13129497..13132046-chr7:13137053..13139000,2	K562	blood:
5	chr7:13086829..13088462-chr7:13155188..13156937,2	K562	blood:
6	chr7:13195077..13196666-chr7:13196806..13198441,2	MCF-7	breast:
7	chr7:13146440..13148600-chr7:13150373..13152655,2	K562	blood:
8	chr7:12678156..12678755-chr7:13218288..13219237,2	MCF-7	breast:
9	chr6:155003966..155004703-chr7:13139161..13140000,2	MCF-7	breast:
10	chr7:12980961..12983258-chr7:13154370..13156023,2	MCF-7	breast:
11	chr7:13187144..13190009-chr7:13193078..13195345,2	K562	blood:
12	chr7:13145074..13147493-chr7:13153724..13155360,2	MCF-7	breast:
13	chr7:13189358..13191512-chr7:13195499..13197059,2	K562	blood:
14	chr7:13134342..13136300-chr7:13222418..13225299,2	MCF-7	breast:
15	chr7:13209664..13212376-chr7:13237521..13239228,2	K562	blood:
16	chr7:12726190..12728016-chr7:13138204..13140895,2	K562	blood:
17	chr7:13187144..13190009-chr7:13193078..13195345,2	K562	blood:
18	chr7:13180182..13182648-chr7:13184471..13186941,2	K562	blood:
19	chr7:12726389..12727416-chr7:13156220..13157643,5	MCF-7	breast:
20	chr7:13212799..13215585-chr7:13218700..13220945,2	K562	blood:
21	chr7:13212799..13215585-chr7:13218700..13220945,2	K562	blood:
22	chr7:13195061..13198037-chr7:13199556..13201286,2	K562	blood:
23	chr7:12726572..12727399-chr7:13154701..13155615,3	MCF-7	breast:
24	chr7:13130850..13133041-chr7:13136588..13139070,3	K562	blood:
25	chr7:12726894..12727511-chr7:13156668..13157359,2	MCF-7	breast:
26	chr7:13195061..13198037-chr7:13199556..13201286,2	K562	blood:
27	chr7:12725278..12725831-chr7:13218360..13219347,3	MCF-7	breast:
28	chr7:12726743..12727464-chr7:13218413..13219282,2	MCF-7	breast:
29	chr7:13146450..13148956-chr7:13151839..13153573,2	MCF-7	breast:
30	chr7:12726065..12729797-chr7:13154020..13158072,4	MCF-7	breast:
31	chr7:13146450..13148956-chr7:13151839..13153573,2	MCF-7	breast:
32	chr7:13180182..13182648-chr7:13184471..13186941,2	K562	blood:
33	chr7:13211183..13213197-chr7:13214894..13216654,2	K562	blood:
34	chr7:13195077..13196666-chr7:13196806..13198441,2	MCF-7	breast:
35	chr7:13146440..13148600-chr7:13150373..13152655,2	K562	blood:
36	chr7:13189358..13191512-chr7:13195499..13197059,2	K562	blood:
37	chr7:12726542..12728897-chr7:13150585..13153553,2	MCF-7	breast:
38	chr7:13145074..13147493-chr7:13153724..13155360,2	MCF-7	breast:
39	chr7:13211183..13213197-chr7:13214894..13216654,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARL4A-1	chr7:13141097-13141208	XLOC_005988

No data

Variant related genes	Relation type
ENSG00000229618	TF binding region
ENSG00000229618	CpG island
ENSG00000122644	chromatin interactions

Extended variants
information (count: 2963 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2963 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12669977	chr7:13132400-13132401	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561035562	chr7:13132403-13132404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559440410	chr7:13132412-13132413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs372979562	chr7:13132433-13132434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183575405	chr7:13132441-13132442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187913596	chr7:13132446-13132447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs141929812	chr7:13132462-13132463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs192475710	chr7:13132497-13132498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs551885669	chr7:13132498-13132499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs61652670	chr7:13132506-13132507	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs537122756	chr7:13132507-13132508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs150245555	chr7:13132553-13132554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs573857141	chr7:13132578-13132579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs111543176	chr7:13132583-13132584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs74540287	chr7:13132585-13132586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537481517	chr7:13132596-13132597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs138921654	chr7:13132602-13132603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572822595	chr7:13132635-13132636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184339110	chr7:13132645-13132646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370368187	chr7:13132652-13132653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs6962533	chr7:13132676-13132677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs572361630	chr7:13132720-13132721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs368350201	chr7:13132721-13132722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs71548010	chr7:13132722-13132723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs7795446	chr7:13132723-13132724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs575004024	chr7:13132755-13132756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs57731200	chr7:13132763-13132764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561703404	chr7:13132765-13132766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs113110397	chr7:13132784-13132785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs80050622	chr7:13132796-13132797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs10251818	chr7:13132824-13132825	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs544276499	chr7:13132850-13132851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561071288	chr7:13132858-13132859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs117480375	chr7:13132859-13132860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs190071631	chr7:13132920-13132921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs560173323	chr7:13132922-13132923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs529833865	chr7:13132939-13132940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs149427712	chr7:13132965-13132966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs551509107	chr7:13132987-13132988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs146406606	chr7:13133043-13133044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs181323580	chr7:13133071-13133072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs199522620	chr7:13133078-13133079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs2058155	chr7:13133124-13133125	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs2058154	chr7:13133162-13133163	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs536422035	chr7:13133221-13133222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563845363	chr7:13133239-13133240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs73678995	chr7:13133242-13133243	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs573471653	chr7:13133277-13133278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77869431	chr7:13133336-13133337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs141550578	chr7:13133341-13133342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:199 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:13130200-13133200	Enhancers	Liver	Liver
2	chr7:13131600-13134000	Enhancers	HUVEC	blood vessel
3	chr7:13132000-13132400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr7:13132200-13132400	Flanking Active TSS	K562	blood
5	chr7:13132200-13132600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr7:13132400-13132600	Enhancers	Primary hematopoietic stem cells	blood
7	chr7:13132400-13132600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr7:13132400-13132600	Enhancers	K562	blood
9	chr7:13132400-13133200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr7:13132600-13133600	Weak transcription	Primary hematopoietic stem cells	blood
11	chr7:13132600-13133600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:13132600-13133600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr7:13133000-13134800	Enhancers	Fetal Kidney	kidney
14	chr7:13133200-13137000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr7:13133200-13137400	Weak transcription	Liver	Liver
16	chr7:13133600-13134000	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr7:13133600-13134400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr7:13133600-13134600	Enhancers	Primary hematopoietic stem cells	blood
19	chr7:13133600-13134600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr7:13133800-13134600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr7:13134600-13143600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr7:13136000-13136200	Enhancers	HepG2	liver
23	chr7:13136200-13143400	Weak transcription	HepG2	liver
24	chr7:13137000-13139600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr7:13137400-13138200	Enhancers	Liver	Liver
26	chr7:13137800-13138200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr7:13138000-13139200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr7:13138000-13139200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr7:13138200-13143400	Weak transcription	Liver	Liver
30	chr7:13138600-13139400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr7:13138600-13139400	Enhancers	HMEC	breast
32	chr7:13138600-13139600	Enhancers	NHEK	skin
33	chr7:13138800-13139200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr7:13138800-13139400	Enhancers	Muscle Satellite Cultured Cells	--
35	chr7:13138800-13139400	Enhancers	A549	lung
36	chr7:13139200-13146600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr7:13139200-13147200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr7:13139800-13140200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr7:13142400-13147600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr7:13143400-13143600	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr7:13143400-13144200	Enhancers	Liver	Liver
42	chr7:13143400-13144400	Enhancers	Stomach Mucosa	stomach
43	chr7:13143400-13144600	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr7:13143400-13144600	Enhancers	HepG2	liver
45	chr7:13143400-13145600	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr7:13143600-13144400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr7:13143600-13144400	Enhancers	K562	blood
48	chr7:13143600-13144400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr7:13144000-13144400	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr7:13144200-13149000	Weak transcription	Liver	Liver

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