Variant report

Variant	nsv457173
Chromosome Location	chr15:58731567-58779039
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1292)
CpG islands
(count:305)
Chromatin interactive
region (count:44)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1292 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:58734368-58734618	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:58767778-58769308	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:58747156-58747675	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:58759096-58761393	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:58761980-58762558	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:58733286-58733314	K562	blood:	n/a	n/a
7	ARID3A	chr15:58755905-58756780	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:58749976-58750707	HepG2	liver:	n/a	n/a
9	ATF1	chr15:58749705-58749952	K562	blood:	n/a	n/a
10	ATF1	chr15:58762340-58762460	K562	blood:	n/a	n/a
11	ATF1	chr15:58759466-58759852	K562	blood:	n/a	n/a
12	ATF1	chr15:58760148-58760226	K562	blood:	n/a	n/a
13	ATF1	chr15:58763625-58763852	K562	blood:	n/a	n/a
14	ATF2	chr15:58765953-58766459	GM12878	blood:	n/a	n/a
15	ATF2	chr15:58746518-58747031	GM12878	blood:	n/a	n/a
16	ATF2	chr15:58765955-58766385	GM12878	blood:	n/a	n/a
17	ATF2	chr15:58749559-58750757	GM12878	blood:	n/a	n/a
18	ATF2	chr15:58746536-58747070	GM12878	blood:	n/a	n/a
19	ATF2	chr15:58749604-58750667	GM12878	blood:	n/a	n/a
20	ATF3	chr15:58762307-58762508	K562	blood:	n/a	n/a
21	ATF3	chr15:58761953-58762623	A549	lung:	n/a	n/a
22	ATF3	chr15:58761860-58762588	A549	lung:	n/a	n/a
23	ATF3	chr15:58732140-58732968	A549	lung:	n/a	n/a
24	ATF3	chr15:58762213-58762548	K562	blood:	n/a	n/a
25	ATF3	chr15:58732131-58733054	A549	lung:	n/a	n/a
26	BACH1	chr15:58734064-58734133	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr15:58759449-58759476	H1-hESC	embryonic stem cell:	n/a	n/a
28	BATF	chr15:58749613-58750100	GM12878	blood:	n/a	chr15:58749825-58749836
29	BATF	chr15:58749589-58750157	GM12878	blood:	n/a	chr15:58749825-58749836
30	BATF	chr15:58750356-58750651	GM12878	blood:	n/a	n/a
31	BATF	chr15:58746555-58746975	GM12878	blood:	n/a	n/a
32	BATF	chr15:58778294-58778642	GM12878	blood:	n/a	n/a
33	BATF	chr15:58746405-58747008	GM12878	blood:	n/a	n/a
34	BATF	chr15:58765883-58766370	GM12878	blood:	n/a	n/a
35	BATF	chr15:58765966-58766352	GM12878	blood:	n/a	n/a
36	BCL11A	chr15:58746609-58746923	GM12878	blood:	n/a	n/a
37	BCL11A	chr15:58749601-58750116	GM12878	blood:	n/a	n/a
38	BCL11A	chr15:58750294-58750729	GM12878	blood:	n/a	chr15:58750499-58750508
39	BCL11A	chr15:58746589-58747023	GM12878	blood:	n/a	n/a
40	BCL11A	chr15:58749655-58750057	GM12878	blood:	n/a	n/a
41	BCL3	chr15:58761726-58762523	A549	lung:	n/a	n/a
42	BCL3	chr15:58746578-58746953	GM12878	blood:	n/a	n/a
43	BCL3	chr15:58732015-58733525	A549	lung:	n/a	n/a
44	BCL3	chr15:58731912-58733673	A549	lung:	n/a	n/a
45	BCL3	chr15:58761757-58762754	A549	lung:	n/a	n/a
46	BCL3	chr15:58749671-58750036	GM12878	blood:	n/a	n/a
47	BCL3	chr15:58749611-58750049	GM12878	blood:	n/a	n/a
48	BCLAF1	chr15:58750270-58750768	GM12878	blood:	n/a	chr15:58750499-58750508
49	BCLAF1	chr15:58746563-58746984	GM12878	blood:	n/a	n/a
50	BCLAF1	chr15:58749579-58750177	GM12878	blood:	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	chr15:58735214-58735264	Hela-S3	cervix:	n/a
2	chr15:58758468-58758518	SK-N-MC	brain:	n/a
3	chr15:58758468-58758518	Hepatocyte	liver:	n/a
4	chr15:58758468-58758518	AoSMC	blood vessel:	n/a
5	chr15:58732754-58732804	NHDF-neo	bronchial:	n/a
6	chr15:58733736-58733786	AG09309	skin:	n/a
7	chr15:58766885-58766935	SK-N-MC	brain:	n/a
8	chr15:58733736-58733786	HepG2	liver:	n/a
9	chr15:58758468-58758518	HAEpiC	amniotic membrane:	n/a
10	chr15:58758468-58758518	SK-N-SH_RA	brain:	n/a
11	chr15:58735214-58735264	PrEC	prostate:	n/a
12	chr15:58732754-58732804	PFSK-1	brain:	n/a
13	chr15:58766885-58766935	HepG2	liver:	n/a
14	chr15:58732754-58732804	GM06990	blood:	n/a
15	chr15:58733736-58733786	Hela-S3	cervix:	n/a
16	chr15:58732754-58732804	LNCaP	prostate:	n/a
17	chr15:58732754-58732804	HCM	heart:	n/a
18	chr15:58732754-58732804	HUVEC	blood vessel:	n/a
19	chr15:58735214-58735264	Caco-2	colon:	n/a
20	chr15:58732754-58732804	IMR90	lung:	fetal
21	chr15:58766885-58766935	HRPEpiC	eye:	n/a
22	chr15:58766885-58766935	LNCaP	prostate:	n/a
23	chr15:58766885-58766935	Hepatocyte	liver:	n/a
24	chr15:58766885-58766935	HUVEC	blood vessel:	n/a
25	chr15:58758468-58758518	SKMC	muscle:	n/a
26	chr15:58758468-58758518	HNPCEpiC	eye:	n/a
27	chr15:58766885-58766935	SAEC	small airway:	n/a
28	chr15:58733736-58733786	AoSMC	blood vessel:	n/a
29	chr15:58733736-58733786	HRCEpiC	kidney:	n/a
30	chr15:58758468-58758518	K562	blood:	n/a
31	chr15:58733736-58733786	GM06990	blood:	n/a
32	chr15:58766885-58766935	HAEpiC	amniotic membrane:	n/a
33	chr15:58732754-58732804	GM12878	blood:	n/a
34	chr15:58732754-58732804	A549	lung:	n/a
35	chr15:58758468-58758518	LNCaP	prostate:	n/a
36	chr15:58766885-58766935	ECC-1	luminal epithelium:	n/a
37	chr15:58735214-58735264	AG10803	skin:	n/a
38	chr15:58732754-58732804	HEEpiC	esophagus:	n/a
39	chr15:58732754-58732804	SAEC	small airway:	n/a
40	chr15:58733736-58733786	HIPEpiC	eye:	n/a
41	chr15:58732754-58732804	HRPEpiC	eye:	n/a
42	chr15:58735214-58735264	HEEpiC	esophagus:	n/a
43	chr15:58766885-58766935	HPAEpiC	pulmonary alveolar:	n/a
44	chr15:58735214-58735264	LNCaP	prostate:	n/a
45	chr15:58732754-58732804	AG04449	skin:	fetal
46	chr15:58758468-58758518	Caco-2	colon:	n/a
47	chr15:58733736-58733786	HAEpiC	amniotic membrane:	n/a
48	chr15:58735214-58735264	GM12878	blood:	n/a
49	chr15:58758468-58758518	PFSK-1	brain:	n/a
50	chr15:58735214-58735264	GM12891	blood:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:58729567..58734283-chr15:58741092..58746394,5	K562	blood:
2	chr15:58767133..58770014-chr15:58770584..58772843,2	MCF-7	breast:
3	chr15:58758547..58760128-chr15:58777523..58780209,2	MCF-7	breast:
4	chr15:58624527..58626111-chr15:58750898..58753049,2	K562	blood:
5	chr15:58758655..58760808-chr15:58812229..58814183,2	MCF-7	breast:
6	chr15:58720668..58723820-chr15:58759148..58762580,3	K562	blood:
7	chr15:58729567..58734283-chr15:58741092..58746394,5	K562	blood:
8	chr15:58758492..58760005-chr15:58885829..58888502,2	MCF-7	breast:
9	chr15:58623562..58626994-chr15:58730618..58733502,3	MCF-7	breast:
10	chr15:58624699..58626357-chr15:58758259..58760422,2	MCF-7	breast:
11	chr15:58732540..58734705-chr15:58743392..58745682,2	MCF-7	breast:
12	chr15:58737118..58738691-chr15:58740817..58742511,2	K562	blood:
13	chr15:58730575..58732285-chr15:58839559..58842370,2	K562	blood:
14	chr15:58742210..58745056-chr15:58745443..58748993,3	K562	blood:
15	chr15:58750305..58752654-chr15:58755983..58757859,3	K562	blood:
16	chr15:58778802..58780678-chr15:58783257..58786951,3	K562	blood:
17	chr15:58726222..58728488-chr15:58751000..58752953,2	K562	blood:
18	chr15:58732540..58734705-chr15:58743392..58745682,2	MCF-7	breast:
19	chr15:58737118..58738691-chr15:58740817..58742511,2	K562	blood:
20	chr15:58742210..58745056-chr15:58745443..58748993,3	K562	blood:
21	chr15:58730817..58731598-chr22:22510997..22511880,2	HCT-116	colon:
22	chr15:58739121..58741793-chr15:58746543..58749268,3	K562	blood:
23	chr15:58623181..58625459-chr15:58764481..58766715,2	MCF-7	breast:
24	chr15:58754820..58757599-chr15:58758355..58762013,3	K562	blood:
25	chr15:58762234..58763977-chr15:59040711..59042531,2	K562	blood:
26	chr15:58739121..58741793-chr15:58746543..58749268,3	K562	blood:
27	chr15:58769989..58771899-chr15:58773674..58776005,2	K562	blood:
28	chr15:58681878..58684869-chr15:58759181..58760747,2	MCF-7	breast:
29	chr15:58731261..58732919-chr15:58735065..58738026,2	K562	blood:
30	chr15:58767751..58769658-chr15:58771265..58773299,2	MCF-7	breast:
31	chr15:58726654..58728474-chr15:58730449..58733344,2	MCF-7	breast:
32	chr15:58754820..58757599-chr15:58758355..58762013,3	K562	blood:
33	chr15:58769989..58771899-chr15:58773674..58776005,2	K562	blood:
34	chr15:58767133..58770014-chr15:58770584..58772843,2	MCF-7	breast:
35	chr15:58762574..58764554-chr15:58812167..58813777,2	K562	blood:
36	chr15:58728810..58730578-chr15:58760180..58761799,2	MCF-7	breast:
37	chr15:58731963..58734945-chr15:58743116..58746394,3	K562	blood:
38	chr15:58731261..58732919-chr15:58735065..58738026,2	K562	blood:
39	chr15:58750305..58752654-chr15:58755983..58757859,3	K562	blood:
40	chr15:58723370..58725024-chr15:58732776..58734366,2	K562	blood:
41	chr15:58758547..58760128-chr15:58777523..58780209,2	MCF-7	breast:
42	chr15:58767751..58769658-chr15:58771265..58773299,2	MCF-7	breast:
43	chr15:58709732..58712579-chr15:58730855..58732681,2	K562	blood:
44	chr15:58731963..58734945-chr15:58743116..58746394,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM10-9	chr15:58765830-58765959	NONHSAT044093

No data

Variant related genes	Relation type
ALDH1A2	TF binding region
ALDH1A2	CpG island
ENSG00000137845	chromatin interactions
ENSG00000259476	chromatin interactions
ENSG00000128918	chromatin interactions
ENSG00000166035	chromatin interactions
ENSG00000233720	chromatin interactions

Extended variants
information (count: 2137 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2137 , 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	rs261341	chr15:58731567-58731568	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs552289112	chr15:58731597-58731598	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs565538377	chr15:58731611-58731612	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs375919707	chr15:58731641-58731642	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs376223968	chr15:58731665-58731666	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs171873	chr15:58731707-58731708	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs547886127	chr15:58731710-58731711	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs567926230	chr15:58731775-58731776	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs545113193	chr15:58731777-58731778	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs111502773	chr15:58731799-58731800	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs8043310	chr15:58731818-58731819	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs570298113	chr15:58731826-58731827	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs564166734	chr15:58731919-58731920	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs12440762	chr15:58731939-58731940	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs188549365	chr15:58731944-58731945	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs572454915	chr15:58731945-58731946	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs370293588	chr15:58732004-58732005	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs541378540	chr15:58732022-58732023	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs191908822	chr15:58732087-58732088	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs185124434	chr15:58732132-58732133	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs574368100	chr15:58732154-58732155	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs145530763	chr15:58732160-58732161	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs190358300	chr15:58732210-58732211	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs563131844	chr15:58732211-58732212	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs114027234	chr15:58732217-58732218	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs16940302	chr15:58732221-58732222	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs559359548	chr15:58732236-58732237	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs35371973	chr15:58732260-58732261	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs528190476	chr15:58732352-58732353	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs548144035	chr15:58732358-58732359	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs182043937	chr15:58732382-58732383	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs530404138	chr15:58732402-58732403	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs372779375	chr15:58732406-58732407	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs550537529	chr15:58732439-58732440	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs12594375	chr15:58732468-58732469	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs529896322	chr15:58732469-58732470	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs368875783	chr15:58732475-58732476	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs558898825	chr15:58732491-58732492	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs549735948	chr15:58732505-58732506	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs566133842	chr15:58732528-58732529	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs148854464	chr15:58732548-58732549	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs59562231	chr15:58732551-58732552	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs185759822	chr15:58732583-58732584	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs543307656	chr15:58732610-58732611	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs113539107	chr15:58732664-58732665	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs577074114	chr15:58732723-58732724	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs561467653	chr15:58732755-58732756	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs532464623	chr15:58732760-58732761	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs188187294	chr15:58732780-58732781	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs376062943	chr15:58732805-58732806	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	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
Colorectal cancer	16774939	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
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1474 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58724800-58732600	Weak transcription	Psoas Muscle	Psoas
2	chr15:58725200-58732000	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr15:58725800-58731800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr15:58726200-58732000	Weak transcription	Fetal Intestine Small	intestine
5	chr15:58726400-58737200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr15:58726600-58731600	Weak transcription	Adipose Nuclei	Adipose
7	chr15:58726600-58732200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr15:58726600-58734200	Weak transcription	Brain Cingulate Gyrus	brain
9	chr15:58726800-58731600	Weak transcription	Stomach Mucosa	stomach
10	chr15:58726800-58732000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr15:58726800-58732000	Weak transcription	HSMM	muscle
12	chr15:58727200-58731600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr15:58728800-58738200	Enhancers	Fetal Thymus	thymus
14	chr15:58729200-58732000	Enhancers	A549	lung
15	chr15:58729200-58733400	Enhancers	Placenta Amnion	Placenta Amnion
16	chr15:58729400-58732000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr15:58729800-58737800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr15:58730000-58732600	Weak transcription	Thymus	Thymus
19	chr15:58730000-58734800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr15:58730000-58737800	Enhancers	HepG2	liver
21	chr15:58730200-58731600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr15:58730200-58732200	Weak transcription	Fetal Heart	heart
23	chr15:58730200-58734400	Enhancers	Pancreas	Pancrea
24	chr15:58730400-58737800	Enhancers	Right Atrium	heart
25	chr15:58730400-58738000	Enhancers	Liver	Liver
26	chr15:58730400-58746200	Weak transcription	GM12878-XiMat	blood
27	chr15:58730600-58732600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr15:58730600-58734600	Enhancers	Right Ventricle	heart
29	chr15:58730800-58735200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr15:58730800-58737800	Enhancers	Left Ventricle	heart
31	chr15:58731000-58731800	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr15:58731000-58732000	Enhancers	Hela-S3	cervix
33	chr15:58731000-58732200	Enhancers	Fetal Muscle Trunk	muscle
34	chr15:58731000-58732400	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr15:58731000-58732800	Enhancers	Duodenum Mucosa	Duodenum
36	chr15:58731000-58734400	Enhancers	Fetal Muscle Leg	muscle
37	chr15:58731000-58734400	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr15:58731000-58735200	Enhancers	Fetal Intestine Large	intestine
39	chr15:58731000-58735600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr15:58731000-58735800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr15:58731200-58731800	Enhancers	Primary T cells from cord blood	blood
42	chr15:58731200-58731800	Enhancers	Esophagus	oesophagus
43	chr15:58731200-58732600	Enhancers	HSMMtube	muscle
44	chr15:58731200-58733000	Weak transcription	Spleen	Spleen
45	chr15:58731200-58734600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr15:58731200-58734600	Enhancers	Placenta	Placenta
47	chr15:58731200-58734800	Enhancers	K562	blood
48	chr15:58731200-58735200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr15:58731200-58736800	Weak transcription	Gastric	stomach
50	chr15:58731200-58736800	Enhancers	NHDF-Ad	bronchial

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