Variant report

Variant	esv2761505
Chromosome Location	chr9:15274373-15319613
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1018)
CpG islands
(count:367)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1018 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:15277823-15278394	HepG2	liver:	n/a	chr9:15278078-15278094
2	ARID3A	chr9:15307077-15307551	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:15280121-15280547	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:15306129-15306386	HepG2	liver:	n/a	n/a
5	ATF1	chr9:15299673-15299858	K562	blood:	n/a	n/a
6	ATF1	chr9:15293783-15294043	K562	blood:	n/a	n/a
7	ATF1	chr9:15287263-15287635	K562	blood:	n/a	n/a
8	BACH1	chr9:15306339-15306925	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr9:15306084-15306387	GM12878	blood:	n/a	n/a
10	BATF	chr9:15299577-15299867	GM12878	blood:	n/a	chr9:15299785-15299794
11	BCL3	chr9:15293395-15293760	GM12878	blood:	n/a	n/a
12	BCLAF1	chr9:15299556-15300027	GM12878	blood:	n/a	chr9:15299645-15299654
13	BHLHE40	chr9:15306190-15306323	K562	blood:	n/a	n/a
14	BHLHE40	chr9:15307178-15307437	GM12878	blood:	n/a	n/a
15	BHLHE40	chr9:15315454-15315624	K562	blood:	n/a	n/a
16	BHLHE40	chr9:15307159-15307687	K562	blood:	n/a	n/a
17	BHLHE40	chr9:15318021-15318086	K562	blood:	n/a	n/a
18	BRCA1	chr9:15299127-15299177	GM12878	blood:	n/a	n/a
19	BRCA1	chr9:15307498-15307506	HepG2	liver:	n/a	n/a
20	BRCA1	chr9:15295906-15296187	GM12878	blood:	n/a	n/a
21	CCNT2	chr9:15307181-15307674	K562	blood:	n/a	n/a
22	CEBPB	chr9:15305916-15306307	HepG2	liver:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
23	CEBPB	chr9:15280220-15280525	IMR90	lung:	n/a	n/a
24	CEBPB	chr9:15299423-15299459	A549	lung:	n/a	n/a
25	CEBPB	chr9:15305959-15306418	A549	lung:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
26	CEBPB	chr9:15280205-15280471	K562	blood:	n/a	n/a
27	CEBPB	chr9:15305937-15306330	H1-hESC	embryonic stem cell:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
28	CEBPB	chr9:15305930-15306387	IMR90	lung:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
29	CEBPB	chr9:15308517-15308964	IMR90	lung:	n/a	n/a
30	CEBPB	chr9:15307236-15307631	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr9:15305868-15306420	MCF-7	breast:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
32	CEBPB	chr9:15307255-15307554	HepG2	liver:	n/a	n/a
33	CEBPB	chr9:15280092-15280472	HepG2	liver:	n/a	n/a
34	CEBPB	chr9:15305956-15306331	A549	lung:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
35	CEBPB	chr9:15305937-15306278	K562	blood:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
36	CEBPB	chr9:15305873-15306429	MCF-7	breast:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
37	CEBPB	chr9:15280216-15280461	A549	lung:	n/a	n/a
38	CEBPB	chr9:15293133-15293400	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr9:15280167-15280556	HepG2	liver:	n/a	n/a
40	CEBPB	chr9:15300306-15300491	HepG2	liver:	n/a	n/a
41	CEBPB	chr9:15296139-15296371	HepG2	liver:	n/a	chr9:15296245-15296258 chr9:15296246-15296257
42	CEBPB	chr9:15280254-15280530	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr9:15296111-15296452	HepG2	liver:	n/a	chr9:15296245-15296258 chr9:15296246-15296257
44	CEBPB	chr9:15287317-15287596	K562	blood:	n/a	n/a
45	CEBPB	chr9:15300306-15300673	IMR90	lung:	n/a	n/a
46	CEBPB	chr9:15306044-15306211	HepG2	liver:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
47	CEBPB	chr9:15280215-15280496	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr9:15293126-15293447	HepG2	liver:	n/a	n/a
49	CEBPB	chr9:15280175-15280554	HepG2	liver:	n/a	n/a
50	CEBPB	chr9:15280136-15280476	HepG2	liver:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:15305873-15305923	HAEpiC	amniotic membrane:	n/a
2	chr9:15305873-15305923	HAEpiC	amniotic membrane:	n/a
3	chr9:15307873-15307923	HepG2	liver:	n/a
4	chr9:15310979-15311029	IMR90	lung:	fetal
5	chr9:15307376-15307426	RPTEC	kidney:	n/a
6	chr9:15310979-15311029	GM12891	blood:	n/a
7	chr9:15307376-15307426	AG10803	skin:	n/a
8	chr9:15306337-15306387	A549	lung:	n/a
9	chr9:15305873-15305923	BE2_C	brain:	n/a
10	chr9:15307873-15307923	T-47D	breast:	n/a
11	chr9:15305873-15305923	PrEC	prostate:	n/a
12	chr9:15307873-15307923	HCF	heart:	n/a
13	chr9:15310979-15311029	HMEC	breast:	n/a
14	chr9:15307873-15307923	HCM	heart:	n/a
15	chr9:15306736-15306786	HNPCEpiC	eye:	n/a
16	chr9:15306337-15306387	HMEC	breast:	n/a
17	chr9:15306337-15306387	RPTEC	kidney:	n/a
18	chr9:15310979-15311029	HPAEpiC	pulmonary alveolar:	n/a
19	chr9:15310979-15311029	AG09319	gingival:	n/a
20	chr9:15307873-15307923	CMK	blood:	n/a
21	chr9:15307376-15307426	HL-60	blood:	n/a
22	chr9:15305873-15305923	AG09309	skin:	n/a
23	chr9:15306736-15306786	AG04449	skin:	fetal
24	chr9:15307376-15307426	SKMC	muscle:	n/a
25	chr9:15306736-15306786	LNCaP	prostate:	n/a
26	chr9:15307376-15307426	ECC-1	luminal epithelium:	n/a
27	chr9:15307873-15307923	HUVEC	blood vessel:	n/a
28	chr9:15306736-15306786	Jurkat	blood:	n/a
29	chr9:15307873-15307923	SAEC	small airway:	n/a
30	chr9:15310979-15311029	AG04449	skin:	fetal
31	chr9:15307376-15307426	IMR90	lung:	fetal
32	chr9:15307376-15307426	GM12892	blood:	n/a
33	chr9:15307376-15307426	HRCEpiC	kidney:	n/a
34	chr9:15307873-15307923	RPTEC	kidney:	n/a
35	chr9:15306337-15306387	SKMC	muscle:	n/a
36	chr9:15306337-15306387	BJ	skin:	n/a
37	chr9:15306736-15306786	AG09309	skin:	n/a
38	chr9:15306736-15306786	HMEC	breast:	n/a
39	chr9:15306736-15306786	HIPEpiC	eye:	n/a
40	chr9:15306337-15306387	SK-N-MC	brain:	n/a
41	chr9:15305873-15305923	HRCEpiC	kidney:	n/a
42	chr9:15306736-15306786	Hela-S3	cervix:	n/a
43	chr9:15307376-15307426	Hepatocyte	liver:	n/a
44	chr9:15307376-15307426	Jurkat	blood:	n/a
45	chr9:15306337-15306387	Jurkat	blood:	n/a
46	chr9:15306736-15306786	PANC-1	pancreas:	n/a
47	chr9:15307873-15307923	NT2-D1	testis:	n/a
48	chr9:15306736-15306786	HRPEpiC	eye:	n/a
49	chr9:15307376-15307426	HUVEC	blood vessel:	n/a
50	chr9:15305873-15305923	AoSMC	blood vessel:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:15283042..15284645-chr9:15287369..15289731,2	K562	blood:
2	chr9:15281113..15283116-chr9:15421375..15424271,2	MCF-7	breast:
3	chr9:15218010..15219971-chr9:15288500..15290967,2	MCF-7	breast:
4	chr9:15300090..15302521-chr9:15304681..15306725,2	MCF-7	breast:
5	chr9:15273681..15276030-chr9:15420461..15422928,2	MCF-7	breast:
6	chr9:15285917..15290029-chr9:15305142..15308889,4	MCF-7	breast:
7	chr9:15306135..15309581-chr9:15420818..15425516,6	MCF-7	breast:
8	chr9:15283111..15284924-chr9:15291453..15293765,2	MCF-7	breast:
9	chr9:15306963..15308773-chr9:15314988..15318754,3	MCF-7	breast:
10	chr9:15276823..15279769-chr9:15280291..15283089,2	MCF-7	breast:
11	chr9:15273274..15274780-chr9:15289457..15291065,2	K562	blood:
12	chr9:15298942..15301605-chr9:15420446..15422025,2	MCF-7	breast:
13	chr9:15303560..15305523-chr9:15350040..15352891,2	MCF-7	breast:
14	chr9:15281310..15283636-chr9:15305576..15307784,3	MCF-7	breast:
15	chr9:15293831..15297894-chr9:15305171..15308300,4	MCF-7	breast:
16	chr9:15300090..15302521-chr9:15304681..15306725,2	MCF-7	breast:
17	chr9:15276823..15279769-chr9:15280291..15283089,2	MCF-7	breast:
18	chr9:15305128..15307154-chr9:15417021..15419951,2	MCF-7	breast:
19	chr9:15276373..15278004-chr9:15420785..15422574,2	MCF-7	breast:
20	chr9:15277764..15278338-chr9:15416698..15417388,2	MCF-7	breast:
21	chr9:15277682..15279519-chr9:15415467..15418240,3	MCF-7	breast:
22	chr9:15275279..15280411-chr9:15305554..15308797,6	MCF-7	breast:
23	chr9:15285882..15288246-chr9:15510557..15512091,2	K562	blood:
24	chr9:15283042..15284645-chr9:15287369..15289731,2	K562	blood:
25	chr9:15298408..15301257-chr9:15344895..15347811,2	MCF-7	breast:
26	chr9:15283111..15284924-chr9:15291453..15293765,2	MCF-7	breast:
27	chr9:15277443..15278337-chr9:15356714..15357650,2	MCF-7	breast:
28	chr9:15273274..15274780-chr9:15289457..15291065,2	K562	blood:
29	chr9:15305088..15306661-chr9:15415103..15416933,2	MCF-7	breast:
30	chr9:15290133..15292362-chr9:15306023..15308672,3	MCF-7	breast:
31	chr9:15278015..15280577-chr9:15305865..15308821,3	MCF-7	breast:

No data

Variant related genes	Relation type
TTC39B	TF binding region
TTC39B	CpG island
ENSG00000155158	chromatin interactions
ENSG00000164985	chromatin interactions
ENSG00000164975	chromatin interactions

Extended variants
information (count: 2111 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2111 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16932898	chr9:15274373-15274374	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184038449	chr9:15274422-15274423	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs536231137	chr9:15274428-15274429	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs57102646	chr9:15274436-15274437	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs370487141	chr9:15274460-15274461	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs139034155	chr9:15274506-15274507	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs550259218	chr9:15274537-15274538	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs565482853	chr9:15274556-15274557	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs112457715	chr9:15274579-15274580	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs114204885	chr9:15274603-15274604	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs556156327	chr9:15274614-15274615	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs566229302	chr9:15274665-15274666	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs188961942	chr9:15274673-15274674	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs368851196	chr9:15274675-15274676	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs548726115	chr9:15274703-15274704	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs139724636	chr9:15274719-15274720	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs77624681	chr9:15274859-15274860	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs141383938	chr9:15274868-15274869	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs34709411	chr9:15274927-15274928	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs28703293	chr9:15274930-15274931	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs77057506	chr9:15274979-15274980	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs527799902	chr9:15274989-15274990	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs546113740	chr9:15275041-15275042	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs572223938	chr9:15275043-15275044	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs575167871	chr9:15275045-15275046	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs542877403	chr9:15275103-15275104	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375223466	chr9:15275117-15275118	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs547757188	chr9:15275152-15275153	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs12342348	chr9:15275159-15275160	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs192994016	chr9:15275186-15275187	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs543981397	chr9:15275203-15275204	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs138140230	chr9:15275227-15275228	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs532792391	chr9:15275235-15275236	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs541618731	chr9:15275249-15275250	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs559871504	chr9:15275253-15275254	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs183613815	chr9:15275275-15275276	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs548821971	chr9:15275281-15275282	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs149590528	chr9:15275285-15275286	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs544104276	chr9:15275286-15275287	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs12342467	chr9:15275291-15275292	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs140531557	chr9:15275298-15275299	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs142788540	chr9:15275320-15275321	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs115442933	chr9:15275328-15275329	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs12347250	chr9:15275341-15275342	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs2849048	chr9:15275349-15275350	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs187040999	chr9:15275366-15275367	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs373075452	chr9:15275408-15275409	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs191478713	chr9:15275460-15275461	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs576546146	chr9:15275472-15275473	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs183685122	chr9:15275525-15275526	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	19835627	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:1722 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15238400-15275400	Weak transcription	Fetal Intestine Large	intestine
2	chr9:15240600-15275400	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr9:15241200-15286200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr9:15243000-15293400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr9:15249600-15276200	Weak transcription	Fetal Kidney	kidney
6	chr9:15249800-15276200	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr9:15250200-15288200	Weak transcription	Fetal Stomach	stomach
8	chr9:15253800-15286400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr9:15254000-15293000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr9:15254200-15275400	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr9:15254200-15276600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr9:15254200-15293000	Weak transcription	NHEK	skin
13	chr9:15254200-15295600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr9:15257000-15277800	Weak transcription	Fetal Lung	lung
15	chr9:15257400-15275200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr9:15259200-15293400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr9:15260600-15283000	Weak transcription	Colon Smooth Muscle	Colon
18	chr9:15261800-15279200	Weak transcription	Ovary	ovary
19	chr9:15263000-15276200	Weak transcription	Duodenum Mucosa	Duodenum
20	chr9:15263800-15283000	Weak transcription	Aorta	Aorta
21	chr9:15264200-15285800	Weak transcription	Primary hematopoietic stem cells	blood
22	chr9:15268800-15277400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr9:15271600-15274600	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr9:15272000-15274400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr9:15272200-15276200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr9:15272200-15276400	Weak transcription	Left Ventricle	heart
27	chr9:15273000-15275600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr9:15273000-15276200	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr9:15273600-15274400	Strong transcription	HepG2	liver
30	chr9:15273600-15274600	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr9:15273600-15275000	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr9:15273600-15286000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr9:15273600-15293400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr9:15273800-15274600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr9:15273800-15275000	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr9:15273800-15275600	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr9:15273800-15276400	Weak transcription	Esophagus	oesophagus
38	chr9:15273800-15277400	Weak transcription	Lung	lung
39	chr9:15273800-15280200	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr9:15273800-15282800	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr9:15274000-15275400	Weak transcription	Fetal Intestine Small	intestine
42	chr9:15274000-15276000	Weak transcription	Stomach Mucosa	stomach
43	chr9:15274000-15276400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr9:15274000-15277000	Weak transcription	Gastric	stomach
45	chr9:15274000-15277600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr9:15274000-15286000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr9:15274000-15288400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr9:15274000-15288400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr9:15274200-15274400	Enhancers	Primary T cells from cord blood	blood
50	chr9:15274400-15274600	Enhancers	H9 Cell Line	embryonic stem cell

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