Variant report

Variant	nsv432479
Chromosome Location	chr3:116356010-116454310
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:207)
CpG islands
(count:366)
Chromatin interactive
region (count:3)
LncRNA
region (count:46)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:207 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr3:116414509-116414701	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr3:116380110-116380418	A549	lung:	n/a	chr3:116380267-116380276 chr3:116380267-116380276 chr3:116380265-116380276 chr3:116380267-116380276 chr3:116380267-116380278 chr3:116380267-116380276
3	CEBPB	chr3:116380163-116380363	H1-hESC	embryonic stem cell:	n/a	chr3:116380267-116380276 chr3:116380267-116380276 chr3:116380265-116380276 chr3:116380267-116380276 chr3:116380267-116380278 chr3:116380267-116380276
4	CEBPB	chr3:116371261-116371583	A549	lung:	n/a	chr3:116371433-116371444
5	CEBPB	chr3:116409913-116410250	A549	lung:	n/a	chr3:116410093-116410104
6	CEBPB	chr3:116380104-116380421	HepG2	liver:	n/a	chr3:116380267-116380276 chr3:116380267-116380276 chr3:116380265-116380276 chr3:116380267-116380276 chr3:116380267-116380278 chr3:116380267-116380276
7	CEBPB	chr3:116447456-116447605	HepG2	liver:	n/a	n/a
8	CEBPB	chr3:116409918-116410249	HepG2	liver:	n/a	chr3:116410093-116410104
9	CEBPB	chr3:116421337-116421535	A549	lung:	n/a	chr3:116421416-116421427 chr3:116421414-116421431 chr3:116421415-116421426 chr3:116421415-116421428 chr3:116421415-116421428
10	CEBPB	chr3:116409978-116410160	H1-hESC	embryonic stem cell:	n/a	chr3:116410093-116410104
11	CEBPB	chr3:116409929-116410256	IMR90	lung:	n/a	chr3:116410093-116410104
12	CEBPB	chr3:116371294-116371606	H1-hESC	embryonic stem cell:	n/a	chr3:116371433-116371444
13	CEBPB	chr3:116371270-116371597	HepG2	liver:	n/a	chr3:116371433-116371444
14	CEBPB	chr3:116434246-116434422	A549	lung:	n/a	n/a
15	CEBPB	chr3:116380085-116380437	IMR90	lung:	n/a	chr3:116380267-116380276 chr3:116380267-116380276 chr3:116380265-116380276 chr3:116380267-116380276 chr3:116380267-116380278 chr3:116380267-116380276
16	CEBPB	chr3:116447561-116447595	A549	lung:	n/a	n/a
17	CEBPB	chr3:116371274-116371609	IMR90	lung:	n/a	chr3:116371433-116371444
18	CEBPB	chr3:116413104-116413373	A549	lung:	n/a	n/a
19	CEBPB	chr3:116376093-116376293	A549	lung:	n/a	n/a
20	CEBPB	chr3:116447484-116447512	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr3:116447345-116447641	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr3:116376019-116376294	IMR90	lung:	n/a	n/a
23	CEBPB	chr3:116444331-116444582	HepG2	liver:	n/a	chr3:116444424-116444435 chr3:116444426-116444435
24	CEBPB	chr3:116376019-116376253	HepG2	liver:	n/a	n/a
25	CEBPB	chr3:116438399-116438554	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr3:116421243-116421563	HepG2	liver:	n/a	chr3:116421416-116421427 chr3:116421414-116421431 chr3:116421415-116421426 chr3:116421415-116421428 chr3:116421415-116421428
27	CTCF	chr3:116403505-116403565	GM20000	blood:	n/a	n/a
28	CTCF	chr3:116443320-116443470	GM06990	blood:	n/a	n/a
29	CTCF	chr3:116363790-116363828	GM20000	blood:	n/a	n/a
30	CTCF	chr3:116364676-116364715	GM10248	blood:	n/a	n/a
31	CTCF	chr3:116391594-116391617	GM10248	blood:	n/a	n/a
32	CTCF	chr3:116363378-116363381	GM10248	blood:	n/a	n/a
33	CTCF	chr3:116444280-116444430	HMF	breast:	n/a	n/a
34	CTCF	chr3:116364617-116364669	Medullo	brain:	n/a	n/a
35	CTCF	chr3:116378940-116379090	GM12865	blood:	n/a	n/a
36	CTCF	chr3:116371800-116371838	Lung_OC	lung:	n/a	n/a
37	E2F4	chr3:116426821-116427076	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr3:116427740-116427854	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr3:116385776-116386039	MCF10A-Er-Src	breast:	n/a	n/a
40	ELK1	chr3:116440958-116440977	Hela-S3	cervix:	n/a	n/a
41	FOS	chr3:116371276-116371517	MCF10A-Er-Src	breast:	n/a	chr3:116371335-116371342 chr3:116371334-116371343 chr3:116371327-116371339 chr3:116371333-116371343 chr3:116371332-116371344 chr3:116371334-116371342
42	FOS	chr3:116379240-116379296	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr3:116385743-116386041	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr3:116385724-116386075	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr3:116380087-116380365	MCF10A-Er-Src	breast:	n/a	chr3:116380334-116380346
46	FOS	chr3:116447471-116447598	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr3:116370039-116370222	MCF10A-Er-Src	breast:	n/a	chr3:116370060-116370068 chr3:116370060-116370068 chr3:116370060-116370067
48	FOS	chr3:116422638-116422940	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr3:116422621-116422947	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr3:116371255-116371516	MCF10A-Er-Src	breast:	n/a	chr3:116371335-116371342 chr3:116371334-116371343 chr3:116371327-116371339 chr3:116371333-116371343 chr3:116371332-116371344 chr3:116371334-116371342

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:116366327-116366377	HRPEpiC	eye:	n/a
2	chr3:116428385-116428435	GM19239	blood:	n/a
3	chr3:116366327-116366377	A549	lung:	n/a
4	chr3:116437373-116437423	K562	blood:	n/a
5	chr3:116428610-116428660	GM12891	blood:	n/a
6	chr3:116428385-116428435	MCF-7	breast:	n/a
7	chr3:116432221-116432271	H1-hESC	embryonic stem cell:	embryo
8	chr3:116428101-116428151	HEK293	kidney:	embryo
9	chr3:116428101-116428151	T-47D	breast:	n/a
10	chr3:116432221-116432271	HRCEpiC	kidney:	n/a
11	chr3:116428385-116428435	NHBE	bronchial:	n/a
12	chr3:116428101-116428151	NT2-D1	testis:	n/a
13	chr3:116437373-116437423	HUVEC	blood vessel:	n/a
14	chr3:116366327-116366377	NHBE	bronchial:	n/a
15	chr3:116428101-116428151	PFSK-1	brain:	n/a
16	chr3:116437373-116437423	HRPEpiC	eye:	n/a
17	chr3:116428610-116428660	MCF-7	breast:	n/a
18	chr3:116428610-116428660	Hela-S3	cervix:	n/a
19	chr3:116428101-116428151	HCF	heart:	n/a
20	chr3:116366327-116366377	BJ	skin:	n/a
21	chr3:116437373-116437423	HCT-116	colon:	n/a
22	chr3:116428101-116428151	HepG2	liver:	n/a
23	chr3:116428385-116428435	ovcar-3	ovarian:	n/a
24	chr3:116432221-116432271	BJ	skin:	n/a
25	chr3:116432221-116432271	HMEC	breast:	n/a
26	chr3:116428610-116428660	AG09319	gingival:	n/a
27	chr3:116428101-116428151	LNCaP	prostate:	n/a
28	chr3:116366327-116366377	AoSMC	blood vessel:	n/a
29	chr3:116366327-116366377	AG09309	skin:	n/a
30	chr3:116432221-116432271	GM06990	blood:	n/a
31	chr3:116437373-116437423	HL-60	blood:	n/a
32	chr3:116366327-116366377	PANC-1	pancreas:	n/a
33	chr3:116428385-116428435	PrEC	prostate:	n/a
34	chr3:116428610-116428660	U87	brain:	n/a
35	chr3:116437373-116437423	BJ	skin:	n/a
36	chr3:116428385-116428435	SAEC	small airway:	n/a
37	chr3:116432221-116432271	GM12878	blood:	n/a
38	chr3:116432221-116432271	NHDF-neo	bronchial:	n/a
39	chr3:116437373-116437423	NHBE	bronchial:	n/a
40	chr3:116432221-116432271	HEK293	kidney:	embryo
41	chr3:116437373-116437423	HCPEpiC	choroid plexus:	n/a
42	chr3:116432221-116432271	AG04449	skin:	fetal
43	chr3:116428101-116428151	Caco-2	colon:	n/a
44	chr3:116428101-116428151	ECC-1	luminal epithelium:	n/a
45	chr3:116437373-116437423	MCF10A-Er-Src	breast:	n/a
46	chr3:116428101-116428151	GM12891	blood:	n/a
47	chr3:116428101-116428151	SK-N-SH_RA	brain:	n/a
48	chr3:116428101-116428151	Hepatocyte	liver:	n/a
49	chr3:116432221-116432271	NH-A	brain:	n/a
50	chr3:116428101-116428151	HCM	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:116446011..116448567-chr3:116450501..116453384,2	K562	blood:
2	chr3:116446011..116448567-chr3:116450501..116453384,2	K562	blood:
3	chr3:116317000..116318575-chr3:116380678..116383155,2	K562	blood:

(count:46 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GAP43-6	chr3:116432886-116432997	NONHSAT091315
2	lnc-GAP43-6	chr3:116432886-116432997	ENSG00000243197.1
3	lnc-GAP43-6	chr3:116428606-116428723	ENSG00000243197.3
4	lnc-GAP43-6	chr3:116435035-116435278	ENSG00000243197.1
5	lnc-GAP43-6	chr3:116432886-116432997	ENSG00000243197.3
6	lnc-GAP43-6	chr3:116432886-116432997	ENSG00000243197.1
7	lnc-GAP43-6	chr3:116428816-116429268	ENSG00000243197.1
8	lnc-GAP43-6	chr3:116431202-116431704	ENSG00000243197.1
9	lnc-GAP43-6	chr3:116432886-116432997	NONHSAT091316
10	lnc-GAP43-6	chr3:116435035-116435278	ENSG00000243197.1
11	lnc-GAP43-6	chr3:116432886-116432997	ENSG00000243197.1
12	lnc-GAP43-6	chr3:116428680-116428723	ENSG00000243197.1
13	lnc-GAP43-6	chr3:116431202-116431704	NONHSAT091317
14	lnc-GAP43-6	chr3:116435035-116435817	NONHSAT091317
15	lnc-GAP43-6	chr3:116429051-116429268	ENSG00000243197.1
16	lnc-GAP43-6	chr3:116435035-116435878	ENSG00000243197.1
17	lnc-GAP43-6	chr3:116428671-116428907	ENSG00000243197.1
18	lnc-GAP43-6	chr3:116436608-116436765	ENSG00000243197.1
19	lnc-GAP43-6	chr3:116428636-116428907	NONHSAT091316
20	lnc-GAP43-6	chr3:116431202-116431318	ENSG00000243197.1
21	lnc-GAP43-6	chr3:116442199-116442428	ENSG00000243197.1
22	lnc-GAP43-6	chr3:116431202-116431318	ENSG00000243197.3
23	lnc-GAP43-6	chr3:116428253-116429268	ENSG00000243197.3
24	lnc-GAP43-6	chr3:116435035-116435817	NONHSAT091316
25	lnc-GAP43-6	chr3:116435035-116435887	NONHSAT091315
26	lnc-GAP43-6	chr3:116429051-116429268	NONHSAT091316
27	lnc-GAP43-6	chr3:116431202-116431354	ENSG00000243197.1
28	lnc-GAP43-6	chr3:116435035-116435174	ENSG00000243197.3
29	lnc-GAP43-6	chr3:116431202-116431354	NONHSAT091316
30	lnc-GAP43-6	chr3:116432886-116432997	NONHSAT091317
31	lnc-GAP43-6	chr3:116429051-116429268	ENSG00000243197.3
32	lnc-GAP43-6	chr3:116431202-116431704	ENSG00000243197.3
33	lnc-GAP43-6	chr3:116428635-116429268	NONHSAT091315
34	lnc-GAP43-6	chr3:116428082-116428907	ENSG00000243197.3
35	lnc-GAP43-6	chr3:116428626-116429268	ENSG00000243197.1
36	lnc-GAP43-6	chr3:116428636-116428723	NONHSAT091317
37	lnc-GAP43-6	chr3:116428626-116428723	ENSG00000243197.1
38	lnc-GAP43-6	chr3:116431202-116431354	ENSG00000243197.3
39	lnc-GAP43-6	chr3:116432886-116432997	ENSG00000243197.1
40	lnc-GAP43-6	chr3:116428816-116429268	ENSG00000243197.1
41	lnc-GAP43-6	chr3:116431202-116431446	ENSG00000243197.1
42	lnc-GAP43-6	chr3:116435035-116436168	ENSG00000243197.3
43	lnc-GAP43-6	chr3:116435035-116435282	ENSG00000243197.1
44	lnc-GAP43-6	chr3:116431202-116431354	ENSG00000243197.1
45	lnc-GAP43-6	chr3:116432886-116432997	ENSG00000243197.3
46	lnc-GAP43-6	chr3:116431202-116431704	NONHSAT091315

No data

Variant related genes	Relation type
BZW1P2	TF binding region
TUSC7	TF binding region
BZW1P2	CpG island
TUSC7	CpG island

Extended variants
information (count: 2310 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2310 , 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	rs150694198	chr3:116359045-116359046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs552368864	chr3:116359095-116359096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559340564	chr3:116359101-116359102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184393722	chr3:116359153-116359154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs528245591	chr3:116359201-116359202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs369040238	chr3:116359260-116359261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs546318935	chr3:116359267-116359268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189074652	chr3:116359269-116359270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs528407482	chr3:116359313-116359314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs532054222	chr3:116359382-116359383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550550532	chr3:116359386-116359387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568717260	chr3:116359394-116359395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs548546790	chr3:116359532-116359533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs536966291	chr3:116359535-116359536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192409962	chr3:116359537-116359538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs112530763	chr3:116359555-116359556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs534375544	chr3:116359563-116359564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs185886134	chr3:116359578-116359579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577264983	chr3:116359588-116359589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs537696133	chr3:116359627-116359628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556413042	chr3:116359658-116359659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574677459	chr3:116359670-116359671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542985254	chr3:116359713-116359714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537472058	chr3:116359717-116359718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560966233	chr3:116359828-116359829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs149822762	chr3:116359829-116359830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540336754	chr3:116359833-116359834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565087253	chr3:116359903-116359904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs9868095	chr3:116359942-116359943	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs78388224	chr3:116359968-116359969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371075801	chr3:116359983-116359984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563177457	chr3:116359992-116359993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs74601661	chr3:116360005-116360006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs75916903	chr3:116360024-116360025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566484389	chr3:116360048-116360049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533825373	chr3:116360063-116360064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189145234	chr3:116360130-116360131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570494045	chr3:116360175-116360176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553539785	chr3:116360178-116360179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144804854	chr3:116360214-116360215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377724468	chr3:116360246-116360247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556112840	chr3:116360257-116360258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs13083720	chr3:116360291-116360292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374286331	chr3:116360345-116360346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201927024	chr3:116360380-116360381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574645207	chr3:116360460-116360461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535374770	chr3:116360463-116360464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554500645	chr3:116360464-116360465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs113874457	chr3:116360488-116360489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs199806803	chr3:116360499-116360500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Ovarian cancer	22174824	CNVD
Myelofibrosis	22110671	CNVD
Characteristic facial feature	22180640	CNVD
hypoplastic male genitals	22180640	CNVD
postnatal overgrowth	22180640	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:116359000-116359800	Enhancers	Adipose Nuclei	Adipose
2	chr3:116359200-116359800	Enhancers	Fetal Brain Male	brain
3	chr3:116359800-116361400	Weak transcription	Fetal Brain Male	brain
4	chr3:116361400-116362400	Enhancers	Fetal Brain Male	brain
5	chr3:116362400-116368000	Weak transcription	Fetal Brain Male	brain
6	chr3:116367000-116368800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr3:116367200-116368000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr3:116367800-116368400	Enhancers	NHEK	skin
9	chr3:116368000-116368400	Enhancers	Fetal Brain Male	brain
10	chr3:116368000-116370200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr3:116368800-116371400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr3:116370000-116370600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr3:116370200-116370400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr3:116371400-116371600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr3:116371600-116379200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr3:116373400-116373800	Enhancers	Brain Cingulate Gyrus	brain
17	chr3:116373400-116373800	Enhancers	Brain Hippocampus Middle	brain
18	chr3:116379200-116380800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr3:116379400-116382200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr3:116380800-116382000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr3:116381400-116382600	Enhancers	Brain Substantia Nigra	brain
22	chr3:116381800-116382600	Enhancers	Rectal Smooth Muscle	rectum
23	chr3:116381800-116382800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr3:116382000-116382800	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr3:116382000-116383000	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr3:116382200-116382800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr3:116382200-116382800	Enhancers	Fetal Stomach	stomach
28	chr3:116382200-116383000	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr3:116382200-116383000	Enhancers	Brain Cingulate Gyrus	brain
30	chr3:116382200-116383000	Enhancers	Brain Hippocampus Middle	brain
31	chr3:116382400-116382600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr3:116382400-116382800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr3:116382400-116382800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr3:116382400-116382800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
35	chr3:116382400-116383000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr3:116382600-116383000	Enhancers	Brain Angular Gyrus	brain
37	chr3:116382600-116387400	Weak transcription	Brain Substantia Nigra	brain
38	chr3:116382800-116383200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr3:116382800-116386800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr3:116383000-116383800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr3:116383000-116387400	Weak transcription	Brain Hippocampus Middle	brain
42	chr3:116383000-116387600	Weak transcription	Brain Angular Gyrus	brain
43	chr3:116383000-116387600	Weak transcription	Brain Cingulate Gyrus	brain
44	chr3:116383000-116392800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr3:116387200-116388200	Enhancers	Brain Anterior Caudate	brain
46	chr3:116387400-116388800	Enhancers	Brain Hippocampus Middle	brain
47	chr3:116387400-116388800	Enhancers	Brain Substantia Nigra	brain
48	chr3:116387600-116388000	Enhancers	Brain Angular Gyrus	brain
49	chr3:116387600-116389600	Enhancers	Brain Cingulate Gyrus	brain
50	chr3:116387800-116390600	Enhancers	Brain Inferior Temporal Lobe	brain

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