Variant report

Variant	nsv437536
Chromosome Location	chr7:13100035-13152162
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:271)
CpG islands
(count:61)
Chromatin interactive
region (count:29)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:271 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:13143855-13144055	K562	blood:	n/a	n/a
2	ARID3A	chr7:13143806-13144072	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:13106506-13106882	K562	blood:	n/a	n/a
4	ARID3A	chr7:13131747-13132382	K562	blood:	n/a	n/a
5	ARID3A	chr7:13138761-13139142	HepG2	liver:	n/a	n/a
6	ATF1	chr7:13143829-13144112	K562	blood:	n/a	n/a
7	ATF1	chr7:13131823-13132227	K562	blood:	n/a	n/a
8	ATF3	chr7:13131828-13132223	K562	blood:	n/a	n/a
9	BACH1	chr7:13112061-13112090	K562	blood:	n/a	n/a
10	BATF	chr7:13138876-13139164	GM12878	blood:	n/a	chr7:13139007-13139018
11	BATF	chr7:13138851-13139153	GM12878	blood:	n/a	chr7:13139007-13139018
12	BHLHE40	chr7:13138027-13138202	K562	blood:	n/a	n/a
13	BHLHE40	chr7:13138780-13139161	HepG2	liver:	n/a	n/a
14	BHLHE40	chr7:13131711-13132161	K562	blood:	n/a	n/a
15	CBX3	chr7:13121526-13121869	K562	blood:	n/a	n/a
16	CBX3	chr7:13149470-13149761	K562	blood:	n/a	n/a
17	CCNT2	chr7:13106658-13106903	K562	blood:	n/a	n/a
18	CCNT2	chr7:13131842-13132210	K562	blood:	n/a	n/a
19	CEBPB	chr7:13100691-13101228	MCF-7	breast:	n/a	chr7:13101041-13101054
20	CEBPB	chr7:13144926-13145120	HepG2	liver:	n/a	chr7:13145038-13145051 chr7:13145038-13145049 chr7:13145040-13145051
21	CEBPB	chr7:13131831-13132213	K562	blood:	n/a	n/a
22	CEBPB	chr7:13131738-13132322	K562	blood:	n/a	n/a
23	CEBPB	chr7:13136917-13137388	K562	blood:	n/a	chr7:13136945-13136958 chr7:13137277-13137288
24	CEBPB	chr7:13147374-13147981	A549	lung:	n/a	chr7:13147889-13147897
25	CEBPB	chr7:13104912-13105118	IMR90	lung:	n/a	chr7:13105009-13105026 chr7:13105011-13105022
26	CEBPB	chr7:13138810-13139178	IMR90	lung:	n/a	n/a
27	CEBPB	chr7:13112897-13113089	K562	blood:	n/a	n/a
28	CEBPB	chr7:13138823-13139128	HepG2	liver:	n/a	n/a
29	CEBPB	chr7:13144858-13145220	HepG2	liver:	n/a	chr7:13145038-13145051 chr7:13145038-13145049 chr7:13145040-13145051
30	CEBPB	chr7:13144878-13145220	K562	blood:	n/a	chr7:13145038-13145051 chr7:13145038-13145049 chr7:13145040-13145051
31	CEBPB	chr7:13147629-13147716	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr7:13144953-13145094	K562	blood:	n/a	chr7:13145038-13145051 chr7:13145038-13145049 chr7:13145040-13145051
33	CEBPB	chr7:13137093-13137536	Hela-S3	cervix:	n/a	chr7:13137277-13137288
34	CEBPB	chr7:13143857-13144090	K562	blood:	n/a	n/a
35	CEBPB	chr7:13104877-13105087	HepG2	liver:	n/a	chr7:13105009-13105026 chr7:13105011-13105022
36	CEBPB	chr7:13143804-13144134	HepG2	liver:	n/a	n/a
37	CEBPB	chr7:13137196-13137417	HepG2	liver:	n/a	chr7:13137277-13137288
38	CEBPB	chr7:13131935-13132211	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr7:13138823-13139120	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr7:13147885-13147964	K562	blood:	n/a	chr7:13147889-13147897
41	CEBPB	chr7:13131816-13132430	IMR90	lung:	n/a	n/a
42	CEBPB	chr7:13131796-13132307	K562	blood:	n/a	n/a
43	CEBPB	chr7:13147632-13147985	HepG2	liver:	n/a	chr7:13147889-13147897
44	CEBPB	chr7:13107448-13107760	K562	blood:	n/a	n/a
45	CEBPB	chr7:13107472-13107767	HepG2	liver:	n/a	n/a
46	CEBPD	chr7:13131819-13132267	K562	blood:	n/a	n/a
47	CEBPD	chr7:13131821-13132359	K562	blood:	n/a	n/a
48	CHD2	chr7:13138909-13138962	GM12878	blood:	n/a	n/a
49	CTCF	chr7:13106877-13106997	K562	blood:	n/a	n/a
50	CTCF	chr7:13146260-13146410	NHDF-neo	bronchial:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:13141735-13141785	Hela-S3	cervix:	n/a
2	chr7:13141735-13141785	HepG2	liver:	n/a
3	chr7:13141735-13141785	HEK293	kidney:	embryo
4	chr7:13141735-13141785	SK-N-SH	brain:	n/a
5	chr7:13141735-13141785	ovcar-3	ovarian:	n/a
6	chr7:13141735-13141785	HNPCEpiC	eye:	n/a
7	chr7:13141735-13141785	U87	brain:	n/a
8	chr7:13141735-13141785	GM19239	blood:	n/a
9	chr7:13141735-13141785	AG04450	lung:	fetal
10	chr7:13141735-13141785	A549	lung:	n/a
11	chr7:13141735-13141785	SK-N-SH_RA	brain:	n/a
12	chr7:13141735-13141785	HCPEpiC	choroid plexus:	n/a
13	chr7:13141735-13141785	HCM	heart:	n/a
14	chr7:13141735-13141785	PrEC	prostate:	n/a
15	chr7:13141735-13141785	Jurkat	blood:	n/a
16	chr7:13141735-13141785	NB4	blood:	n/a
17	chr7:13141735-13141785	K562	blood:	n/a
18	chr7:13141735-13141785	RPTEC	kidney:	n/a
19	chr7:13141735-13141785	HCF	heart:	n/a
20	chr7:13141735-13141785	T-47D	breast:	n/a
21	chr7:13141735-13141785	HEEpiC	esophagus:	n/a
22	chr7:13141735-13141785	HAEpiC	amniotic membrane:	n/a
23	chr7:13141735-13141785	NHDF-neo	bronchial:	n/a
24	chr7:13141735-13141785	AG09309	skin:	n/a
25	chr7:13141735-13141785	AoSMC	blood vessel:	n/a
26	chr7:13141735-13141785	GM12891	blood:	n/a
27	chr7:13141735-13141785	NT2-D1	testis:	n/a
28	chr7:13141735-13141785	SKMC	muscle:	n/a
29	chr7:13141735-13141785	GM12878	blood:	n/a
30	chr7:13141735-13141785	HUVEC	blood vessel:	n/a
31	chr7:13141735-13141785	BE2_C	brain:	n/a
32	chr7:13141735-13141785	GM06990	blood:	n/a
33	chr7:13141735-13141785	ECC-1	luminal epithelium:	n/a
34	chr7:13141735-13141785	ProgFib	skin:	n/a
35	chr7:13141735-13141785	AG10803	skin:	n/a
36	chr7:13141735-13141785	NHBE	bronchial:	n/a
37	chr7:13141735-13141785	IMR90	lung:	fetal
38	chr7:13141735-13141785	CMK	blood:	n/a
39	chr7:13141735-13141785	NH-A	brain:	n/a
40	chr7:13141735-13141785	AG04449	skin:	fetal
41	chr7:13141735-13141785	HRE	kidney:	n/a
42	chr7:13141735-13141785	PANC-1	pancreas:	n/a
43	chr7:13141735-13141785	HMEC	breast:	n/a
44	chr7:13141735-13141785	BJ	skin:	n/a
45	chr7:13141735-13141785	SK-N-MC	brain:	n/a
46	chr7:13141735-13141785	PFSK-1	brain:	n/a
47	chr7:13141735-13141785	MCF-7	breast:	n/a
48	chr7:13141735-13141785	HIPEpiC	eye:	n/a
49	chr7:13141735-13141785	HCT-116	colon:	n/a
50	chr7:13141735-13141785	HPAEpiC	pulmonary alveolar:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:13129497..13132046-chr7:13137053..13139000,2	K562	blood:
2	chr7:12726190..12728016-chr7:13138204..13140895,2	K562	blood:
3	chr7:12776917..12778957-chr7:13100732..13103715,2	MCF-7	breast:
4	chr7:13146440..13148600-chr7:13150373..13152655,2	K562	blood:
5	chr7:12724403..12726396-chr7:13103717..13106545,2	K562	blood:
6	chr7:13130850..13133041-chr7:13136588..13139070,3	K562	blood:
7	chr7:13099163..13101911-chr7:13106498..13108964,2	K562	blood:
8	chr7:13095947..13098043-chr7:13101119..13103304,2	MCF-7	breast:
9	chr7:13111805..13113325-chr7:13115222..13117599,2	K562	blood:
10	chr7:13111805..13113325-chr7:13115222..13117599,2	K562	blood:
11	chr7:13100363..13102009-chr7:13102221..13104284,2	K562	blood:
12	chr7:13145074..13147493-chr7:13153724..13155360,2	MCF-7	breast:
13	chr7:13099163..13101911-chr7:13106498..13108964,2	K562	blood:
14	chr7:13146450..13148956-chr7:13151839..13153573,2	MCF-7	breast:
15	chr7:13105294..13107639-chr7:13110167..13112332,4	K562	blood:
16	chr7:13104322..13106884-chr7:13107040..13109324,2	K562	blood:
17	chr7:13104322..13106884-chr7:13107040..13109324,2	K562	blood:
18	chr7:12726542..12728897-chr7:13150585..13153553,2	MCF-7	breast:
19	chr7:12730592..12732679-chr7:13123373..13125180,2	K562	blood:
20	chr7:13105294..13107639-chr7:13110167..13112332,4	K562	blood:
21	chr7:13134342..13136300-chr7:13222418..13225299,2	MCF-7	breast:
22	chr7:13146440..13148600-chr7:13150373..13152655,2	K562	blood:
23	chr7:13146450..13148956-chr7:13151839..13153573,2	MCF-7	breast:
24	chr7:13100363..13102009-chr7:13102221..13104284,2	K562	blood:
25	chr7:13093779..13096148-chr7:13099334..13101239,2	K562	blood:
26	chr7:13129497..13132046-chr7:13137053..13139000,2	K562	blood:
27	chr7:13130850..13133041-chr7:13136588..13139070,3	K562	blood:
28	chr7:13085851..13087402-chr7:13106082..13107771,2	K562	blood:
29	chr6:155003966..155004703-chr7:13139161..13140000,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARL4A-7	chr7:13107541-13107733	NONHSAT119247
2	lnc-ARL4A-7	chr7:13108158-13108539	NONHSAT119247
3	lnc-ARL4A-7	chr7:13107622-13107733	NONHSAT119248
4	lnc-ARL4A-1	chr7:13141097-13141208	XLOC_005988

No data

Variant related genes	Relation type
ENSG00000229618	TF binding region
ENSG00000229618	CpG island
ENSG00000271253	chromatin interactions
ENSG00000122644	chromatin interactions

Extended variants
information (count: 2092 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2092 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10488244	chr7:13100035-13100036	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571651628	chr7:13100229-13100230	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs140292885	chr7:13100233-13100234	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs386710474	chr7:13100296-13100297	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs17166683	chr7:13100301-13100302	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs73678981	chr7:13100358-13100359	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs553529605	chr7:13100415-13100416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573499916	chr7:13100444-13100445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146484811	chr7:13100450-13100451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs367717326	chr7:13100456-13100457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554326693	chr7:13100524-13100525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs7809888	chr7:13100536-13100537	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs543773494	chr7:13100601-13100602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs560656820	chr7:13100653-13100654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs116219705	chr7:13100672-13100673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs540099752	chr7:13100723-13100724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs560283727	chr7:13100748-13100749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533766057	chr7:13100779-13100780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531144708	chr7:13100791-13100792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs13245067	chr7:13100876-13100877	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs562744588	chr7:13100930-13100931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs35370595	chr7:13100954-13100955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs530944098	chr7:13100972-13100973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188923495	chr7:13101000-13101001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs73678982	chr7:13101008-13101009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567701515	chr7:13101020-13101021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs193247919	chr7:13101024-13101025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546912754	chr7:13101036-13101037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs76839327	chr7:13101038-13101039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs11983822	chr7:13101058-13101059	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs148280165	chr7:13101086-13101087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184680195	chr7:13101196-13101197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs140431725	chr7:13101202-13101203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs187378610	chr7:13101221-13101222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs574486199	chr7:13101224-13101225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs147040434	chr7:13101231-13101232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546092985	chr7:13101236-13101237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs553711719	chr7:13101243-13101244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs191783662	chr7:13101245-13101246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs34760917	chr7:13101248-13101249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs77402467	chr7:13101249-13101250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562774596	chr7:13101276-13101277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs531635424	chr7:13101279-13101280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs17166686	chr7:13101300-13101301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs561320724	chr7:13101304-13101305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs138356888	chr7:13101312-13101313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547094880	chr7:13101361-13101362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566821009	chr7:13101374-13101375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs371982578	chr7:13101401-13101402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184048503	chr7:13101410-13101411	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:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:13090200-13102600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:13095000-13103800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr7:13100200-13100400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr7:13100400-13104000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:13100600-13101400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr7:13101000-13101600	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr7:13101200-13103000	Enhancers	Fetal Intestine Large	intestine
8	chr7:13101400-13101800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr7:13101400-13103600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr7:13101800-13102800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr7:13101800-13103000	Enhancers	Fetal Intestine Small	intestine
12	chr7:13102400-13102800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr7:13102400-13103000	Enhancers	HepG2	liver
14	chr7:13102600-13102800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr7:13103000-13106800	Weak transcription	HepG2	liver
16	chr7:13103600-13104200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr7:13103800-13104200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr7:13103800-13104200	Enhancers	NHEK	skin
19	chr7:13104000-13104200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr7:13104000-13104400	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr7:13104400-13109400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr7:13106400-13106600	Enhancers	K562	blood
23	chr7:13106600-13107000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr7:13106600-13107000	Flanking Active TSS	K562	blood
25	chr7:13106800-13107400	Enhancers	HepG2	liver
26	chr7:13107000-13117400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr7:13109400-13112000	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr7:13111200-13112200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr7:13111400-13111800	Enhancers	Colon Smooth Muscle	Colon
30	chr7:13111400-13112200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr7:13111600-13112200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr7:13111800-13112200	Enhancers	NHEK	skin
33	chr7:13112200-13113200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr7:13112200-13116600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr7:13112200-13116600	Weak transcription	NHEK	skin
36	chr7:13113200-13113400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr7:13116200-13118000	Enhancers	Muscle Satellite Cultured Cells	--
38	chr7:13116600-13116800	Enhancers	HMEC	breast
39	chr7:13116600-13117000	Enhancers	HSMMtube	muscle
40	chr7:13116600-13117600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr7:13116600-13117600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr7:13116600-13117600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr7:13116600-13117800	Enhancers	HSMM	muscle
44	chr7:13116600-13117800	Enhancers	HUVEC	blood vessel
45	chr7:13116600-13117800	Enhancers	NHEK	skin
46	chr7:13116600-13117800	Enhancers	Osteobl	bone
47	chr7:13116600-13118000	Enhancers	NH-A	brain
48	chr7:13116600-13118400	Enhancers	A549	lung
49	chr7:13116800-13117800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr7:13117400-13117600	Enhancers	HMEC	breast

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