Variant report

Variant	nsv904273
Chromosome Location	chr15:59518488-59567137
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1260)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1260 , 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	chr15:59548038-59548642	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:59565522-59565778	HepG2	liver:	n/a	n/a
3	ATF2	chr15:59543290-59544016	GM12878	blood:	n/a	n/a
4	ATF2	chr15:59529132-59529867	GM12878	blood:	n/a	n/a
5	ATF2	chr15:59541516-59541956	GM12878	blood:	n/a	n/a
6	ATF2	chr15:59541530-59542251	GM12878	blood:	n/a	n/a
7	ATF2	chr15:59536469-59536953	GM12878	blood:	n/a	n/a
8	ATF2	chr15:59529116-59530436	GM12878	blood:	n/a	n/a
9	ATF2	chr15:59543177-59543945	GM12878	blood:	n/a	n/a
10	ATF3	chr15:59547934-59549201	A549	lung:	n/a	n/a
11	ATF3	chr15:59547896-59548708	A549	lung:	n/a	n/a
12	BATF	chr15:59536559-59536907	GM12878	blood:	n/a	n/a
13	BATF	chr15:59560403-59560703	GM12878	blood:	n/a	chr15:59560656-59560666
14	BATF	chr15:59543388-59543832	GM12878	blood:	n/a	chr15:59543634-59543645
15	BATF	chr15:59548297-59548544	GM12878	blood:	n/a	n/a
16	BATF	chr15:59545118-59545418	GM12878	blood:	n/a	n/a
17	BATF	chr15:59541512-59541972	GM12878	blood:	n/a	chr15:59541717-59541728
18	BATF	chr15:59543443-59543805	GM12878	blood:	n/a	chr15:59543634-59543645
19	BATF	chr15:59529378-59529699	GM12878	blood:	n/a	n/a
20	BATF	chr15:59541513-59541853	GM12878	blood:	n/a	chr15:59541717-59541728
21	BATF	chr15:59529408-59529684	GM12878	blood:	n/a	n/a
22	BCL11A	chr15:59543386-59543830	GM12878	blood:	n/a	n/a
23	BCL11A	chr15:59548261-59548536	GM12878	blood:	n/a	chr15:59548461-59548468
24	BCL11A	chr15:59541516-59541885	GM12878	blood:	n/a	n/a
25	BCL11A	chr15:59529285-59529735	GM12878	blood:	n/a	n/a
26	BCL11A	chr15:59541601-59541845	GM12878	blood:	n/a	n/a
27	BCL11A	chr15:59536616-59536907	GM12878	blood:	n/a	n/a
28	BCL11A	chr15:59548298-59548565	GM12878	blood:	n/a	chr15:59548461-59548468
29	BCL11A	chr15:59536616-59536902	GM12878	blood:	n/a	n/a
30	BCL3	chr15:59541569-59541834	GM12878	blood:	n/a	n/a
31	BCL3	chr15:59547717-59549145	A549	lung:	n/a	chr15:59548461-59548468
32	BCL3	chr15:59565249-59565972	A549	lung:	n/a	chr15:59565903-59565910
33	BCL3	chr15:59547834-59549080	A549	lung:	n/a	chr15:59548461-59548468
34	BCLAF1	chr15:59539502-59539992	GM12878	blood:	n/a	n/a
35	BCLAF1	chr15:59529235-59530496	GM12878	blood:	n/a	chr15:59529999-59530008
36	BCLAF1	chr15:59536586-59537074	GM12878	blood:	n/a	n/a
37	BCLAF1	chr15:59541546-59541883	GM12878	blood:	n/a	n/a
38	BCLAF1	chr15:59543355-59543946	GM12878	blood:	n/a	n/a
39	BCLAF1	chr15:59542899-59543381	GM12878	blood:	n/a	n/a
40	BHLHE40	chr15:59560563-59560626	GM12878	blood:	n/a	n/a
41	BHLHE40	chr15:59548328-59548592	GM12878	blood:	n/a	n/a
42	BHLHE40	chr15:59544501-59544517	GM12878	blood:	n/a	n/a
43	BHLHE40	chr15:59565393-59565676	HepG2	liver:	n/a	n/a
44	BHLHE40	chr15:59541503-59542366	GM12878	blood:	n/a	n/a
45	BHLHE40	chr15:59543359-59544098	GM12878	blood:	n/a	n/a
46	BHLHE40	chr15:59536540-59536999	GM12878	blood:	n/a	n/a
47	BHLHE40	chr15:59529306-59530436	GM12878	blood:	n/a	n/a
48	BRCA1	chr15:59526334-59526363	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr15:59560263-59561583	Hela-S3	cervix:	n/a	chr15:59560671-59560678
50	BRCA1	chr15:59547873-59549469	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:59524009-59524059	CMK	blood:	n/a
2	chr15:59524009-59524059	LNCaP	prostate:	n/a
3	chr15:59524009-59524059	HepG2	liver:	n/a
4	chr15:59524009-59524059	AoSMC	blood vessel:	n/a
5	chr15:59524009-59524059	IMR90	lung:	fetal
6	chr15:59524009-59524059	HCM	heart:	n/a
7	chr15:59524009-59524059	HCT-116	colon:	n/a
8	chr15:59524009-59524059	ovcar-3	ovarian:	n/a
9	chr15:59524009-59524059	PrEC	prostate:	n/a
10	chr15:59524009-59524059	HL-60	blood:	n/a
11	chr15:59524009-59524059	HRPEpiC	eye:	n/a
12	chr15:59524009-59524059	BJ	skin:	n/a
13	chr15:59524009-59524059	GM19239	blood:	n/a
14	chr15:59524009-59524059	HMEC	breast:	n/a
15	chr15:59524009-59524059	SK-N-SH_RA	brain:	n/a
16	chr15:59524009-59524059	H1-hESC	embryonic stem cell:	embryo
17	chr15:59524009-59524059	MCF10A-Er-Src	breast:	n/a
18	chr15:59524009-59524059	HCPEpiC	choroid plexus:	n/a
19	chr15:59524009-59524059	MCF-7	breast:	n/a
20	chr15:59524009-59524059	HRCEpiC	kidney:	n/a
21	chr15:59524009-59524059	NT2-D1	testis:	n/a
22	chr15:59524009-59524059	PFSK-1	brain:	n/a
23	chr15:59524009-59524059	SAEC	small airway:	n/a
24	chr15:59524009-59524059	AG04449	skin:	fetal
25	chr15:59524009-59524059	RPTEC	kidney:	n/a
26	chr15:59524009-59524059	GM12892	blood:	n/a
27	chr15:59524009-59524059	ECC-1	luminal epithelium:	n/a
28	chr15:59524009-59524059	HPAEpiC	pulmonary alveolar:	n/a
29	chr15:59524009-59524059	AG10803	skin:	n/a
30	chr15:59524009-59524059	HCF	heart:	n/a
31	chr15:59524009-59524059	NH-A	brain:	n/a
32	chr15:59524009-59524059	A549	lung:	n/a
33	chr15:59524009-59524059	HRE	kidney:	n/a
34	chr15:59524009-59524059	T-47D	breast:	n/a
35	chr15:59524009-59524059	NHDF-neo	bronchial:	n/a
36	chr15:59524009-59524059	Hela-S3	cervix:	n/a
37	chr15:59524009-59524059	AG09309	skin:	n/a
38	chr15:59524009-59524059	HAEpiC	amniotic membrane:	n/a
39	chr15:59524009-59524059	Jurkat	blood:	n/a
40	chr15:59524009-59524059	HEK293	kidney:	embryo
41	chr15:59524009-59524059	U87	brain:	n/a
42	chr15:59524009-59524059	HIPEpiC	eye:	n/a
43	chr15:59524009-59524059	SK-N-MC	brain:	n/a
44	chr15:59524009-59524059	GM12891	blood:	n/a
45	chr15:59524009-59524059	ProgFib	skin:	n/a
46	chr15:59524009-59524059	SK-N-SH	brain:	n/a
47	chr15:59524009-59524059	Caco-2	colon:	n/a
48	chr15:59524009-59524059	GM06990	blood:	n/a
49	chr15:59524009-59524059	K562	blood:	n/a
50	chr15:59524009-59524059	BE2_C	brain:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:59563253..59565075-chr15:59566378..59568169,2	K562	blood:
2	chr15:59552086..59554457-chr15:59559341..59561438,2	K562	blood:
3	chr15:59538258..59540187-chr15:59575748..59578001,2	MCF-7	breast:
4	chr15:59565954..59568631-chr15:59980553..59982430,2	K562	blood:
5	chr15:59536729..59539462-chr15:59542944..59544488,2	K562	blood:
6	chr15:59554788..59557654-chr15:59562989..59565608,2	K562	blood:
7	chr15:59536729..59539462-chr15:59542944..59544488,2	K562	blood:
8	chr15:59552086..59554457-chr15:59559341..59561438,2	K562	blood:
9	chr15:59554788..59557654-chr15:59562989..59565608,2	K562	blood:
10	chr15:59539485..59542336-chr15:59663424..59665650,3	MCF-7	breast:
11	chr15:59559608..59563212-chr15:59663665..59667768,4	MCF-7	breast:
12	chr15:59539475..59539997-chr15:59704300..59705075,2	MCF-7	breast:
13	chr15:59518511..59521491-chr15:59664302..59666468,2	MCF-7	breast:
14	chr15:59561146..59562823-chr15:59949552..59951074,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLTM-3	chr15:59558919-59559114	ENSG00000259771.1
2	lnc-SLTM-9	chr15:59563530-59563953	NONHSAT044161
3	lnc-SLTM-3	chr15:59563110-59563361	ENSG00000259771.1

No data

Variant related genes	Relation type
MYO1E	TF binding region
ENSG00000259771	TF binding region
MYO1E	CpG island
ENSG00000259771	CpG island
ENSG00000259771	chromatin interactions
ENSG00000157483	chromatin interactions
ENSG00000157470	chromatin interactions
ENSG00000140307	chromatin interactions
ENSG00000140299	chromatin interactions
ENSG00000259238	chromatin interactions

Extended variants
information (count: 2342 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2342 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11631023	chr15:59518488-59518489	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs562218055	chr15:59518498-59518499	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77853529	chr15:59518542-59518543	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs74741366	chr15:59518547-59518548	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs76322712	chr15:59518550-59518551	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs79025539	chr15:59518551-59518552	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs9672463	chr15:59518555-59518556	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs140712107	chr15:59518601-59518602	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs566350780	chr15:59518659-59518660	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs563617592	chr15:59518706-59518707	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs552125097	chr15:59518716-59518717	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs191406493	chr15:59518743-59518744	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs537505056	chr15:59518749-59518750	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs80182222	chr15:59518778-59518779	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs550402404	chr15:59518782-59518783	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs184709408	chr15:59518795-59518796	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs34253780	chr15:59518813-59518814	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs147848154	chr15:59518891-59518892	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs7167255	chr15:59518897-59518898	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs113083877	chr15:59518929-59518930	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs572283431	chr15:59518950-59518951	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs73422980	chr15:59519014-59519015	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs531797712	chr15:59519020-59519021	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs146977609	chr15:59519053-59519054	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs138046187	chr15:59519062-59519063	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs190029392	chr15:59519114-59519115	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs7166294	chr15:59519133-59519134	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs36120684	chr15:59519158-59519159	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs529547487	chr15:59519186-59519187	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs547951509	chr15:59519194-59519195	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs547080854	chr15:59519196-59519197	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs149155626	chr15:59519206-59519207	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs571035166	chr15:59519276-59519277	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs533612545	chr15:59519304-59519305	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs562095672	chr15:59519319-59519320	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs192808659	chr15:59519329-59519330	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs185316454	chr15:59519356-59519357	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs143293594	chr15:59519357-59519358	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs567799148	chr15:59519378-59519379	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs151225252	chr15:59519417-59519418	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs535318028	chr15:59519429-59519430	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs148286090	chr15:59519433-59519434	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs189336335	chr15:59519448-59519449	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs539674526	chr15:59519469-59519470	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs73422983	chr15:59519473-59519474	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs529532192	chr15:59519475-59519476	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs543823649	chr15:59519497-59519498	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs34475456	chr15:59519529-59519530	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs555928431	chr15:59519540-59519541	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs574156603	chr15:59519577-59519578	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
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
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
Mental retardation	17124404	CNVD
Gastrointestinal stromal cancer	20877625	CNVD

Chromatin state (count:1308 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:59467800-59523200	Weak transcription	Fetal Brain Female	brain
2	chr15:59468200-59528600	Weak transcription	Stomach Mucosa	stomach
3	chr15:59468600-59521400	Strong transcription	Rectal Mucosa Donor 29	rectum
4	chr15:59485600-59521200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr15:59487800-59524400	Weak transcription	Small Intestine	intestine
6	chr15:59492000-59521600	Strong transcription	Rectal Mucosa Donor 31	rectum
7	chr15:59493200-59523200	Strong transcription	Hela-S3	cervix
8	chr15:59496800-59522000	Strong transcription	NHEK	skin
9	chr15:59497000-59524800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr15:59498800-59522000	Strong transcription	GM12878-XiMat	blood
11	chr15:59500000-59524400	Weak transcription	Right Ventricle	heart
12	chr15:59500600-59524600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr15:59501200-59521400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr15:59501200-59523400	Weak transcription	Ovary	ovary
15	chr15:59501200-59525600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr15:59502800-59525800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr15:59504000-59520200	Strong transcription	Liver	Liver
18	chr15:59511400-59549200	Weak transcription	Colonic Mucosa	Colon
19	chr15:59512200-59521600	Strong transcription	Fetal Intestine Small	intestine
20	chr15:59512600-59520000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr15:59513400-59520200	Strong transcription	Primary B cells from peripheral blood	blood
22	chr15:59513400-59521600	Strong transcription	Fetal Intestine Large	intestine
23	chr15:59514800-59521400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr15:59514800-59521400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr15:59514800-59524200	Weak transcription	Colon Smooth Muscle	Colon
26	chr15:59515000-59519200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr15:59515000-59524400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr15:59515200-59521400	Strong transcription	Osteobl	bone
29	chr15:59515400-59523800	Weak transcription	Rectal Smooth Muscle	rectum
30	chr15:59515600-59521600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr15:59515800-59519800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr15:59515800-59522000	Strong transcription	HMEC	breast
33	chr15:59515800-59566600	Weak transcription	Pancreas	Pancrea
34	chr15:59516000-59519400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr15:59516200-59519400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr15:59516400-59519000	Weak transcription	NH-A	brain
37	chr15:59516400-59522800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr15:59516400-59524600	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr15:59516600-59519000	Strong transcription	NHDF-Ad	bronchial
40	chr15:59516600-59519400	Weak transcription	HSMMtube	muscle
41	chr15:59516600-59524400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr15:59516600-59529400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr15:59516800-59522800	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr15:59516800-59523200	Weak transcription	Stomach Smooth Muscle	stomach
45	chr15:59517000-59519400	Strong transcription	Fetal Stomach	stomach
46	chr15:59517000-59521000	Weak transcription	Brain Angular Gyrus	brain
47	chr15:59517000-59521200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr15:59517000-59524200	Strong transcription	HSMM	muscle
49	chr15:59517000-59530200	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr15:59517000-59536600	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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