Variant report

Variant	nsv570242
Chromosome Location	chr15:82370616-82409727
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:936)
CpG islands
(count:305)
Chromatin interactive
region (count:25)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:936 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:82395869-82396118	K562	blood:	n/a	n/a
2	ARID3A	chr15:82401001-82401002	K562	blood:	n/a	n/a
3	ARID3A	chr15:82386098-82386477	K562	blood:	n/a	n/a
4	ARID3A	chr15:82374412-82374413	K562	blood:	n/a	n/a
5	ARID3A	chr15:82402621-82402884	K562	blood:	n/a	n/a
6	ATF1	chr15:82402666-82402887	K562	blood:	n/a	n/a
7	ATF1	chr15:82386057-82386548	K562	blood:	n/a	n/a
8	ATF3	chr15:82386007-82386455	K562	blood:	n/a	n/a
9	BACH1	chr15:82397969-82397981	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr15:82372902-82373188	GM12878	blood:	n/a	n/a
11	BCL3	chr15:82391074-82391291	GM12878	blood:	n/a	n/a
12	BHLHE40	chr15:82386095-82386510	K562	blood:	n/a	n/a
13	BHLHE40	chr15:82374424-82374533	K562	blood:	n/a	n/a
14	BHLHE40	chr15:82378992-82379159	K562	blood:	n/a	n/a
15	BHLHE40	chr15:82400843-82401102	K562	blood:	n/a	n/a
16	BHLHE40	chr15:82395922-82396071	K562	blood:	n/a	n/a
17	BHLHE40	chr15:82396298-82396499	K562	blood:	n/a	n/a
18	BRCA1	chr15:82386082-82386445	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr15:82386086-82386521	K562	blood:	n/a	n/a
20	CBX3	chr15:82400839-82401263	K562	blood:	n/a	n/a
21	CCNT2	chr15:82402576-82402788	K562	blood:	n/a	n/a
22	CCNT2	chr15:82379090-82379273	K562	blood:	n/a	chr15:82379122-82379142
23	CCNT2	chr15:82374339-82374522	K562	blood:	n/a	n/a
24	CCNT2	chr15:82386130-82386485	K562	blood:	n/a	n/a
25	CEBPB	chr15:82386068-82386458	K562	blood:	n/a	chr15:82386244-82386255
26	CEBPB	chr15:82395084-82395398	A549	lung:	n/a	n/a
27	CEBPB	chr15:82386011-82386541	IMR90	lung:	n/a	chr15:82386244-82386255
28	CEBPB	chr15:82386025-82386510	K562	blood:	n/a	chr15:82386244-82386255
29	CEBPB	chr15:82383979-82384330	IMR90	lung:	n/a	n/a
30	CEBPB	chr15:82395191-82395267	K562	blood:	n/a	n/a
31	CEBPB	chr15:82386008-82386564	Hela-S3	cervix:	n/a	chr15:82386244-82386255
32	CEBPB	chr15:82392940-82393048	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr15:82385996-82386610	A549	lung:	n/a	chr15:82386244-82386255
34	CEBPB	chr15:82383993-82384303	K562	blood:	n/a	n/a
35	CEBPB	chr15:82383960-82384377	MCF-7	breast:	n/a	n/a
36	CEBPB	chr15:82383982-82384317	A549	lung:	n/a	n/a
37	CEBPB	chr15:82386077-82386411	K562	blood:	n/a	chr15:82386244-82386255
38	CEBPB	chr15:82382298-82382448	A549	lung:	n/a	n/a
39	CEBPB	chr15:82381317-82381476	HepG2	liver:	n/a	n/a
40	CEBPB	chr15:82398274-82398612	IMR90	lung:	n/a	chr15:82398429-82398442
41	CEBPB	chr15:82381200-82381390	IMR90	lung:	n/a	chr15:82381247-82381260
42	CEBPB	chr15:82395049-82395325	HepG2	liver:	n/a	n/a
43	CEBPB	chr15:82386086-82386434	HepG2	liver:	n/a	chr15:82386244-82386255
44	CEBPB	chr15:82395085-82395305	IMR90	lung:	n/a	n/a
45	CEBPB	chr15:82392963-82393112	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr15:82386054-82386470	A549	lung:	n/a	chr15:82386244-82386255
47	CEBPB	chr15:82386060-82386499	A549	lung:	n/a	chr15:82386244-82386255
48	CEBPD	chr15:82402486-82402919	K562	blood:	n/a	n/a
49	CHD2	chr15:82400931-82401160	HepG2	liver:	n/a	n/a
50	CHD2	chr15:82386096-82386465	HepG2	liver:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:82379947-82379997	HCPEpiC	choroid plexus:	n/a
2	chr15:82379883-82379933	BJ	skin:	n/a
3	chr15:82379883-82379933	SAEC	small airway:	n/a
4	chr15:82379947-82379997	PANC-1	pancreas:	n/a
5	chr15:82379947-82379997	AoSMC	blood vessel:	n/a
6	chr15:82393236-82393286	HMEC	breast:	n/a
7	chr15:82381568-82381618	SAEC	small airway:	n/a
8	chr15:82379883-82379933	GM12892	blood:	n/a
9	chr15:82374456-82374506	AG10803	skin:	n/a
10	chr15:82393236-82393286	LNCaP	prostate:	n/a
11	chr15:82379947-82379997	GM12878	blood:	n/a
12	chr15:82393236-82393286	CMK	blood:	n/a
13	chr15:82374456-82374506	GM12892	blood:	n/a
14	chr15:82379883-82379933	Hela-S3	cervix:	n/a
15	chr15:82379883-82379933	HEEpiC	esophagus:	n/a
16	chr15:82379947-82379997	Hepatocyte	liver:	n/a
17	chr15:82379947-82379997	AG09309	skin:	n/a
18	chr15:82393236-82393286	HNPCEpiC	eye:	n/a
19	chr15:82374456-82374506	AoSMC	blood vessel:	n/a
20	chr15:82374456-82374506	SAEC	small airway:	n/a
21	chr15:82374456-82374506	ECC-1	luminal epithelium:	n/a
22	chr15:82379883-82379933	HNPCEpiC	eye:	n/a
23	chr15:82374456-82374506	Hela-S3	cervix:	n/a
24	chr15:82379883-82379933	AoSMC	blood vessel:	n/a
25	chr15:82393236-82393286	IMR90	lung:	fetal
26	chr15:82393236-82393286	AG04450	lung:	fetal
27	chr15:82374456-82374506	HEK293	kidney:	embryo
28	chr15:82381568-82381618	NHBE	bronchial:	n/a
29	chr15:82379947-82379997	ovcar-3	ovarian:	n/a
30	chr15:82379947-82379997	SK-N-SH	brain:	n/a
31	chr15:82374456-82374506	HAEpiC	amniotic membrane:	n/a
32	chr15:82381568-82381618	HNPCEpiC	eye:	n/a
33	chr15:82379947-82379997	NH-A	brain:	n/a
34	chr15:82374456-82374506	K562	blood:	n/a
35	chr15:82393236-82393286	SK-N-MC	brain:	n/a
36	chr15:82393236-82393286	HEK293	kidney:	embryo
37	chr15:82379947-82379997	K562	blood:	n/a
38	chr15:82381568-82381618	H1-hESC	embryonic stem cell:	embryo
39	chr15:82374456-82374506	NHDF-neo	bronchial:	n/a
40	chr15:82379947-82379997	SK-N-MC	brain:	n/a
41	chr15:82379947-82379997	AG04449	skin:	fetal
42	chr15:82381568-82381618	GM12892	blood:	n/a
43	chr15:82393236-82393286	ECC-1	luminal epithelium:	n/a
44	chr15:82393236-82393286	HRPEpiC	eye:	n/a
45	chr15:82379883-82379933	AG04449	skin:	fetal
46	chr15:82393236-82393286	HCT-116	colon:	n/a
47	chr15:82379883-82379933	PFSK-1	brain:	n/a
48	chr15:82379883-82379933	ECC-1	luminal epithelium:	n/a
49	chr15:82379947-82379997	HRCEpiC	kidney:	n/a
50	chr15:82381568-82381618	HRPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr15:82105377..82106205-chr15:82395564..82396156,2	MCF-7	breast:
2	chr15:82390762..82392949-chr15:82398564..82402214,3	K562	blood:
3	chr15:82394736..82396289-chr15:82399463..82401078,2	MCF-7	breast:
4	chr15:82405061..82407968-chr15:82415699..82418455,2	K562	blood:
5	chr15:82338516..82340987-chr15:82386144..82387942,2	MCF-7	breast:
6	chr15:82336811..82339430-chr15:82392148..82395651,3	MCF-7	breast:
7	chr15:82396164..82398346-chr15:82406284..82408349,2	K562	blood:
8	chr15:82401295..82402881-chr15:82407665..82409375,2	K562	blood:
9	chr15:81772882..81773555-chr15:82397557..82398455,2	K562	blood:
10	chr15:82386362..82388607-chr15:82391684..82394477,4	K562	blood:
11	chr15:82401295..82402881-chr15:82407665..82409375,2	K562	blood:
12	chr15:82386362..82388607-chr15:82391684..82394477,4	K562	blood:
13	chr15:82400526..82401456-chr15:82490044..82491282,10	MCF-7	breast:
14	chr15:82337307..82338833-chr15:82401935..82404513,2	MCF-7	breast:
15	chr15:82400531..82401257-chr15:82431919..82432522,2	MCF-7	breast:
16	chr15:82375697..82377432-chr15:82459942..82461886,2	K562	blood:
17	chr15:82396164..82398346-chr15:82406284..82408349,2	K562	blood:
18	chr15:82394736..82396289-chr15:82399463..82401078,2	MCF-7	breast:
19	chr15:82400583..82401510-chr15:82431758..82433239,16	MCF-7	breast:
20	chr15:82400569..82401498-chr15:82490090..82491041,4	K562	blood:
21	chr15:82400510..82401451-chr15:82489931..82491014,9	MCF-7	breast:
22	chr15:82376238..82379058-chr15:82380480..82382562,2	MCF-7	breast:
23	chr15:82336857..82340285-chr15:82395789..82397569,3	MCF-7	breast:
24	chr15:82390762..82392949-chr15:82398564..82402214,3	K562	blood:
25	chr15:82403068..82405226-chr15:82430485..82432551,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-597K23.2.1-1	chr15:82387823-82388777	ENSG00000249946
2	lnc-RP11-597K23.2.1-1	chr15:82386324-82386575	ENSG00000249946
3	lnc-RP11-597K23.2.1-2	chr15:82391267-82391320	XLOC_011331
4	lnc-RP11-597K23.2.1-2	chr15:82390362-82395263	NONHSAT047767
5	lnc-RP11-597K23.2.1-2	chr15:82390245-82390326	NONHSAT047767
6	lnc-RP11-597K23.2.1-1	chr15:82384068-82384945	NONHSAT047766
7	lnc-RP11-597K23.2.1-1	chr15:82389789-82390032	ENSG00000249946
8	lnc-RP11-597K23.2.1-1	chr15:82384068-82384945	ENSG00000249946
9	lnc-RP11-597K23.2.1-1	chr15:82387823-82388777	NONHSAT047766
10	lnc-RP11-597K23.2.1-1	chr15:82385735-82385835	ENSG00000249946
11	lnc-RP11-597K23.2.1-1	chr15:82380935-82381069	NONHSAT047766
12	lnc-RP11-597K23.2.1-1	chr15:82380935-82381069	ENSG00000249946
13	lnc-RP11-597K23.2.1-1	chr15:82389789-82390035	NONHSAT047766
14	lnc-RP11-597K23.2.1-1	chr15:82386324-82386575	NONHSAT047766
15	lnc-RP11-597K23.2.1-2	chr15:82391746-82393834	XLOC_011331
16	lnc-RP11-597K23.2.1-1	chr15:82385735-82385835	NONHSAT047766

No data

Variant related genes	Relation type
ENSG00000259518	TF binding region
ENSG00000259518	CpG island
ENSG00000183496	chromatin interactions
ENSG00000259518	chromatin interactions
C9orf5	miRNA target sites
SUZ12	miRNA target sites
LIMCH1	miRNA target sites
PRRC1	miRNA target sites

Extended variants
information (count: 1530 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1530 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554966848	chr15:82372073-82372074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs574961041	chr15:82372079-82372080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs2654224	chr15:82372104-82372105	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs142458066	chr15:82372105-82372106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532519959	chr15:82372155-82372156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557618825	chr15:82372200-82372201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs577767355	chr15:82372235-82372236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs567283841	chr15:82372277-82372278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146621618	chr15:82372365-82372366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs187914318	chr15:82372370-82372371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191325096	chr15:82372386-82372387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs562081222	chr15:82372407-82372408	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs139117874	chr15:82372423-82372424	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs149362795	chr15:82372435-82372436	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs570896877	chr15:82372530-82372531	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs533555313	chr15:82372535-82372536	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs550640548	chr15:82372536-82372537	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs546906158	chr15:82372649-82372650	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538094154	chr15:82372690-82372691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566794857	chr15:82372751-82372752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535760243	chr15:82372777-82372778	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548527691	chr15:82372794-82372795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568512723	chr15:82372830-82372831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs182351215	chr15:82372831-82372832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs557827595	chr15:82372864-82372865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187923861	chr15:82372865-82372866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs375636756	chr15:82372938-82372939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556546906	chr15:82373015-82373016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562974822	chr15:82373042-82373043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554032413	chr15:82373062-82373063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573949015	chr15:82373082-82373083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192968404	chr15:82373109-82373110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535986719	chr15:82373128-82373129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562451600	chr15:82373129-82373130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35789002	chr15:82373142-82373143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562016976	chr15:82373202-82373203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575591467	chr15:82373216-82373217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544314588	chr15:82373274-82373275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564582673	chr15:82373313-82373314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533286388	chr15:82373316-82373317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547135788	chr15:82373317-82373318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143650359	chr15:82373323-82373324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185158685	chr15:82373324-82373325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548624745	chr15:82373333-82373334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537835513	chr15:82373355-82373356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538863182	chr15:82373397-82373398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199837510	chr15:82373398-82373399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551120571	chr15:82373399-82373400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs199787725	chr15:82373414-82373415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571295253	chr15:82373416-82373417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Congenital diaphragmatic hernia	20921022	CNVD
abnormal development	18461090	CNVD
Intellectual disability	22102821	CNVD
renal disease	17924346	CNVD
Breast cancer	20409316	CNVD
Mental retardation	17847001	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21509527	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:82372000-82372600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr15:82372000-82372600	Enhancers	Fetal Lung	lung
3	chr15:82372000-82372600	Enhancers	Fetal Stomach	stomach
4	chr15:82372200-82372400	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr15:82372200-82372400	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr15:82372200-82373000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr15:82372400-82372600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr15:82372400-82373000	Enhancers	HSMMtube	muscle
9	chr15:82372600-82373600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr15:82372800-82374200	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr15:82373000-82374200	Weak transcription	HSMMtube	muscle
12	chr15:82373000-82374400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr15:82373600-82374200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr15:82374000-82374400	Enhancers	Osteobl	bone
15	chr15:82374000-82375400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr15:82374200-82374800	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr15:82374200-82374800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr15:82374200-82375000	Enhancers	H1 Cell Line	embryonic stem cell
19	chr15:82374200-82375400	Enhancers	HSMMtube	muscle
20	chr15:82374200-82375400	Enhancers	NH-A	brain
21	chr15:82374200-82376000	Enhancers	HSMM	muscle
22	chr15:82374400-82374800	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr15:82374400-82375000	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr15:82374400-82375000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr15:82374400-82375000	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr15:82374400-82375000	Flanking Active TSS	Osteobl	bone
27	chr15:82374400-82375200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr15:82374400-82375400	Enhancers	Muscle Satellite Cultured Cells	--
29	chr15:82374600-82374800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr15:82374600-82374800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr15:82374600-82374800	Enhancers	K562	blood
32	chr15:82374600-82375000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr15:82374600-82375000	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr15:82374600-82375000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr15:82374600-82375000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr15:82374600-82375000	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr15:82374600-82375000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr15:82374600-82375000	Enhancers	NHDF-Ad	bronchial
39	chr15:82374600-82375200	Enhancers	HMEC	breast
40	chr15:82374600-82375400	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr15:82374600-82375400	Enhancers	GM12878-XiMat	blood
42	chr15:82374800-82375000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr15:82374800-82375000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr15:82374800-82375000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr15:82374800-82375400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr15:82374800-82377800	Weak transcription	K562	blood
47	chr15:82375000-82375200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr15:82375000-82375200	Enhancers	Osteobl	bone
49	chr15:82375000-82380600	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr15:82375000-82381000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links