Variant report

Variant	nsv530026
Chromosome Location	chr3:98837320-99340537
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2606)
CpG islands
(count:427)
Chromatin interactive
region (count:34)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2606 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:99223184-99223477	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:99298237-99298263	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:98892032-98892087	HepG2	liver:	n/a	n/a
4	ATF2	chr3:99149199-99150075	GM12878	blood:	n/a	n/a
5	ATF2	chr3:99202618-99203076	GM12878	blood:	n/a	n/a
6	ATF2	chr3:99224596-99225255	GM12878	blood:	n/a	n/a
7	ATF2	chr3:99298711-99299237	GM12878	blood:	n/a	n/a
8	ATF2	chr3:99126018-99126540	GM12878	blood:	n/a	n/a
9	ATF2	chr3:99149054-99150131	GM12878	blood:	n/a	n/a
10	ATF2	chr3:99224637-99225315	GM12878	blood:	n/a	n/a
11	ATF2	chr3:99298779-99299215	GM12878	blood:	n/a	n/a
12	ATF2	chr3:99202558-99203147	GM12878	blood:	n/a	n/a
13	ATF2	chr3:99129459-99130103	GM12878	blood:	n/a	n/a
14	ATF2	chr3:99136767-99138323	GM12878	blood:	n/a	n/a
15	ATF2	chr3:99254161-99254586	GM12878	blood:	n/a	n/a
16	ATF2	chr3:99129338-99130149	GM12878	blood:	n/a	n/a
17	ATF2	chr3:99136810-99138372	GM12878	blood:	n/a	n/a
18	ATF2	chr3:99176777-99177247	GM12878	blood:	n/a	n/a
19	BACH1	chr3:99037775-99038010	H1-hESC	embryonic stem cell:	n/a	chr3:99037826-99037840
20	BATF	chr3:99176890-99177182	GM12878	blood:	n/a	chr3:99177056-99177067
21	BATF	chr3:99202699-99203096	GM12878	blood:	n/a	n/a
22	BATF	chr3:99126158-99126394	GM12878	blood:	n/a	n/a
23	BATF	chr3:99298861-99299109	GM12878	blood:	n/a	chr3:99299001-99299010
24	BATF	chr3:99298802-99299168	GM12878	blood:	n/a	chr3:99299001-99299010
25	BATF	chr3:99129502-99129964	GM12878	blood:	n/a	n/a
26	BATF	chr3:99137044-99137371	GM12878	blood:	n/a	n/a
27	BATF	chr3:99333730-99333931	GM12878	blood:	n/a	chr3:99333785-99333796
28	BATF	chr3:99137541-99137961	GM12878	blood:	n/a	n/a
29	BATF	chr3:99202574-99203096	GM12878	blood:	n/a	n/a
30	BATF	chr3:99149710-99149973	GM12878	blood:	n/a	n/a
31	BATF	chr3:99072300-99072544	GM12878	blood:	n/a	n/a
32	BATF	chr3:99224687-99225114	GM12878	blood:	n/a	n/a
33	BATF	chr3:99254190-99254486	GM12878	blood:	n/a	chr3:99254393-99254403
34	BATF	chr3:99149216-99150020	GM12878	blood:	n/a	n/a
35	BATF	chr3:99136983-99137472	GM12878	blood:	n/a	n/a
36	BATF	chr3:99224726-99225079	GM12878	blood:	n/a	n/a
37	BCL11A	chr3:99149570-99150010	GM12878	blood:	n/a	n/a
38	BCL11A	chr3:99129498-99129865	GM12878	blood:	n/a	n/a
39	BCL11A	chr3:99254160-99254556	GM12878	blood:	n/a	chr3:99254395-99254404
40	BCL11A	chr3:99202609-99203107	GM12878	blood:	n/a	n/a
41	BCL11A	chr3:99224741-99225155	GM12878	blood:	n/a	n/a
42	BCL11A	chr3:99298821-99299191	GM12878	blood:	n/a	n/a
43	BCL11A	chr3:99136984-99137417	GM12878	blood:	n/a	n/a
44	BCL11A	chr3:99137498-99137995	GM12878	blood:	n/a	n/a
45	BCL11A	chr3:99126152-99126384	GM12878	blood:	n/a	chr3:99126235-99126244
46	BCL11A	chr3:99224723-99225108	GM12878	blood:	n/a	n/a
47	BCL11A	chr3:99129594-99129774	GM12878	blood:	n/a	n/a
48	BCL3	chr3:99129441-99130174	GM12878	blood:	n/a	n/a
49	BCL3	chr3:99149673-99150009	GM12878	blood:	n/a	n/a
50	BCL3	chr3:99224696-99225137	GM12878	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:99228156-99228206	HRE	kidney:	n/a
2	chr3:99038751-99038801	A549	lung:	n/a
3	chr3:99193044-99193094	HMEC	breast:	n/a
4	chr3:99038751-99038801	HRPEpiC	eye:	n/a
5	chr3:98848062-98848112	Caco-2	colon:	n/a
6	chr3:99218170-99218220	PFSK-1	brain:	n/a
7	chr3:99228156-99228206	T-47D	breast:	n/a
8	chr3:99013462-99013512	HCPEpiC	choroid plexus:	n/a
9	chr3:99228156-99228206	ECC-1	luminal epithelium:	n/a
10	chr3:99113136-99113186	H1-hESC	embryonic stem cell:	embryo
11	chr3:99038751-99038801	U87	brain:	n/a
12	chr3:99013462-99013512	NHBE	bronchial:	n/a
13	chr3:98848062-98848112	PrEC	prostate:	n/a
14	chr3:98848062-98848112	HRCEpiC	kidney:	n/a
15	chr3:99038751-99038801	SK-N-MC	brain:	n/a
16	chr3:99113136-99113186	HL-60	blood:	n/a
17	chr3:99113136-99113186	CMK	blood:	n/a
18	chr3:99013462-99013512	HPAEpiC	pulmonary alveolar:	n/a
19	chr3:99038751-99038801	HCPEpiC	choroid plexus:	n/a
20	chr3:99228156-99228206	RPTEC	kidney:	n/a
21	chr3:99013462-99013512	HCF	heart:	n/a
22	chr3:99218170-99218220	ECC-1	luminal epithelium:	n/a
23	chr3:99193044-99193094	AG04450	lung:	fetal
24	chr3:99113136-99113186	AG09319	gingival:	n/a
25	chr3:99228156-99228206	Hepatocyte	liver:	n/a
26	chr3:99013462-99013512	NH-A	brain:	n/a
27	chr3:99038751-99038801	SK-N-SH_RA	brain:	n/a
28	chr3:99113136-99113186	PrEC	prostate:	n/a
29	chr3:99113136-99113186	ECC-1	luminal epithelium:	n/a
30	chr3:99228156-99228206	HCF	heart:	n/a
31	chr3:99228156-99228206	AG04450	lung:	fetal
32	chr3:99013462-99013512	K562	blood:	n/a
33	chr3:99113136-99113186	HRPEpiC	eye:	n/a
34	chr3:99113136-99113186	HAEpiC	amniotic membrane:	n/a
35	chr3:99113136-99113186	Jurkat	blood:	n/a
36	chr3:99193044-99193094	HCPEpiC	choroid plexus:	n/a
37	chr3:99113136-99113186	AG04449	skin:	fetal
38	chr3:99228156-99228206	PrEC	prostate:	n/a
39	chr3:99193044-99193094	GM12892	blood:	n/a
40	chr3:99228156-99228206	PANC-1	pancreas:	n/a
41	chr3:99113136-99113186	AG04450	lung:	fetal
42	chr3:99113136-99113186	GM12892	blood:	n/a
43	chr3:99038751-99038801	HCM	heart:	n/a
44	chr3:99038751-99038801	HAEpiC	amniotic membrane:	n/a
45	chr3:99113136-99113186	HCM	heart:	n/a
46	chr3:99193044-99193094	MCF10A-Er-Src	breast:	n/a
47	chr3:99013462-99013512	Jurkat	blood:	n/a
48	chr3:98848062-98848112	U87	brain:	n/a
49	chr3:99113136-99113186	GM06990	blood:	n/a
50	chr3:99193044-99193094	NHDF-neo	bronchial:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:98960467..98962608-chr3:98963910..98966387,2	K562	blood:
2	chr3:99217926..99218471-chr3:99250937..99251667,2	MCF-7	breast:
3	chr3:98839672..98842383-chr3:98845089..98846835,2	K562	blood:
4	chr3:98742090..98742958-chr3:98891307..98892432,5	MCF-7	breast:
5	chr3:98898412..98900467-chr3:98901353..98902956,2	MCF-7	breast:
6	chr3:98833143..98834039-chr3:99250824..99251730,3	MCF-7	breast:
7	chr3:99325508..99327428-chr3:99330801..99332344,2	MCF-7	breast:
8	chr3:98898412..98900467-chr3:98901353..98902956,2	MCF-7	breast:
9	chr3:98833031..98833794-chr3:98891585..98892473,5	MCF-7	breast:
10	chr3:99218147..99219010-chr3:99363822..99364695,3	MCF-7	breast:
11	chr3:99279758..99281912-chr3:99291680..99293883,2	MCF-7	breast:
12	chr3:98960467..98962608-chr3:98963910..98966387,2	K562	blood:
13	chr3:99218086..99218777-chr3:99250976..99251575,3	MCF-7	breast:
14	chr1:245283605..245286595-chr3:99028241..99029743,2	K562	blood:
15	chr3:99217180..99218833-chr3:99471535..99472845,8	MCF-7	breast:
16	chr2:218516301..218518088-chr3:99186166..99188131,2	MCF-7	breast:
17	chr3:99087839..99089975-chr3:99109906..99112170,2	K562	blood:
18	chr3:99265933..99267760-chr3:99267872..99270717,2	K562	blood:
19	chr3:98839672..98842383-chr3:98845089..98846835,2	K562	blood:
20	chr3:99313372..99317178-chr3:99319758..99322601,3	K562	blood:
21	chr3:98742225..98743062-chr3:98891577..98892142,2	MCF-7	breast:
22	chr3:99087839..99089975-chr3:99109906..99112170,2	K562	blood:
23	chr3:99217926..99218471-chr3:99250937..99251667,2	MCF-7	breast:
24	chr3:99250812..99251418-chr3:99471853..99472489,2	MCF-7	breast:
25	chr3:99215007..99217420-chr3:99218950..99221198,2	MCF-7	breast:
26	chr3:99175047..99178537-chr3:99179291..99181710,3	K562	blood:
27	chr3:99218086..99218777-chr3:99250976..99251575,3	MCF-7	breast:
28	chr3:99325508..99327428-chr3:99330801..99332344,2	MCF-7	breast:
29	chr3:99265933..99267760-chr3:99267872..99270717,2	K562	blood:
30	chr3:33332155..33332655-chr3:99159710..99160214,2	Hela-S3	cervix:
31	chr3:99279758..99281912-chr3:99291680..99293883,2	MCF-7	breast:
32	chr3:99175047..99178537-chr3:99179291..99181710,3	K562	blood:
33	chr3:99075499..99077922-chr3:99083475..99085918,2	K562	blood:
34	chr3:99217843..99218709-chr3:99405590..99406505,5	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL8A1-4	chr3:99281139-99281319	l_2412_chr3:99279688-99284179_testes
2	lnc-COL8A1-4	chr3:99284057-99284179	l_2412_chr3:99279688-99284179_testes
3	lnc-COL8A1-2	chr3:99224090-99224352	XLOC_002737
4	lnc-COL8A1-10	chr3:99073376-99074955	l_2411_chr3:99023559-99073456_placenta
5	lnc-COL8A1-10	chr3:99065727-99066181	l_2411_chr3:99023559-99073456_placenta
6	lnc-DCBLD2-2	chr3:98934068-98935110	NONHSAT090839
7	lnc-ST3GAL6-6	chr3:98899387-98899480	NONHSAT090838
8	lnc-COL8A1-2	chr3:99219191-99219385	XLOC_002737
9	lnc-COL8A1-10	chr3:99023560-99023889	l_2411_chr3:99023559-99073456_placenta
10	lnc-COL8A1-7	chr3:99077254-99078457	expReg_chr3_6666_+
11	lnc-COL8A1-1	chr3:99316908-99317343	ENSG00000244464
12	lnc-COL8A1-4	chr3:99279689-99279724	l_2412_chr3:99279688-99284179_testes
13	lnc-ST3GAL6-6	chr3:98896222-98896357	NONHSAT090838
14	lnc-COL8A1-8	chr3:99076755-99077211	expReg_chr3_6665_+
15	lnc-COL8A1-10	chr3:99044729-99044797	l_2411_chr3:99023559-99073456_placenta
16	lnc-ST3GAL6-6	chr3:98904502-98904611	NONHSAT090838
17	lnc-COL8A1-9	chr3:99076197-99076504	expReg_chr3_6662_+

No data

Variant related genes	Relation type
ENSG00000266030	TF binding region
ENSG00000243089	TF binding region
ACTG1P13	TF binding region
ENSG00000240572	TF binding region
ENSG00000243296	TF binding region
ENSG00000244464	TF binding region
ENSG00000266030	CpG island
ENSG00000243089	CpG island
ACTG1P13	CpG island
ENSG00000240572	CpG island
ENSG00000243296	CpG island
ENSG00000244464	CpG island
ENSG00000243296	chromatin interactions
ENSG00000266030	chromatin interactions
ENSG00000244464	chromatin interactions

Extended variants
information (count: 16201 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:16201 , 50 per page) page: 1 2 3 4 5 6 7 ... 325

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573219013	chr3:98837363-98837364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs367863149	chr3:98837402-98837403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538918799	chr3:98837423-98837424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147760993	chr3:98837438-98837439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181248884	chr3:98837443-98837444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs370702838	chr3:98837481-98837482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544783761	chr3:98837522-98837523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs561271372	chr3:98837541-98837542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs555125052	chr3:98837545-98837546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs142642132	chr3:98837570-98837571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs1524218	chr3:98837579-98837580	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs146896846	chr3:98837583-98837584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs185549351	chr3:98837649-98837650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190650171	chr3:98837732-98837733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs562679492	chr3:98837735-98837736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531444268	chr3:98837741-98837742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2966549	chr3:98837749-98837750	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs148355160	chr3:98837761-98837762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs542245442	chr3:98837773-98837774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115349661	chr3:98837781-98837782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs141541859	chr3:98837787-98837788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs62276804	chr3:98837795-98837796	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs1524217	chr3:98837799-98837800	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs182938413	chr3:98837801-98837802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569529390	chr3:98837899-98837900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs538083067	chr3:98837901-98837902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs115279327	chr3:98837946-98837947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs527979034	chr3:98837972-98837973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574851503	chr3:98837978-98837979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs572692093	chr3:98837982-98837983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs72932744	chr3:98837986-98837987	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs189127972	chr3:98837995-98837996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577267433	chr3:98838047-98838048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546208806	chr3:98838062-98838063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546992011	chr3:98838095-98838096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs531620587	chr3:98838202-98838203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs541677301	chr3:98838216-98838217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561896841	chr3:98838239-98838240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs372565454	chr3:98838251-98838252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs543273720	chr3:98838276-98838277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs114480585	chr3:98838292-98838293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs570204317	chr3:98838306-98838307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs75507054	chr3:98838404-98838405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs77464559	chr3:98838405-98838406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs79705363	chr3:98838406-98838407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs77668614	chr3:98838409-98838410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs2966548	chr3:98838412-98838413	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs569484173	chr3:98838443-98838444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs538496376	chr3:98838445-98838446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs567123054	chr3:98838448-98838449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	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
Myelofibrosis	22110671	CNVD
Epilepsy	21858020	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1615 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:98828000-98837800	Weak transcription	NH-A	brain
2	chr3:98828000-98838000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:98834400-98848200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr3:98836000-98838400	Enhancers	HSMM	muscle
5	chr3:98836200-98838400	Enhancers	HSMMtube	muscle
6	chr3:98836800-98839400	Enhancers	NHDF-Ad	bronchial
7	chr3:98837000-98838400	Enhancers	NHLF	lung
8	chr3:98837000-98838800	Enhancers	Osteobl	bone
9	chr3:98837200-98838000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr3:98837200-98838400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr3:98837200-98838800	Enhancers	Muscle Satellite Cultured Cells	--
12	chr3:98837200-98839400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr3:98837600-98838600	Enhancers	HMEC	breast
14	chr3:98837800-98838800	Enhancers	NH-A	brain
15	chr3:98838000-98838400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr3:98838000-98838400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr3:98838000-98838600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr3:98838000-98838800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr3:98838000-98839400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr3:98838400-98843800	Weak transcription	HSMMtube	muscle
21	chr3:98838400-98844600	Weak transcription	HSMM	muscle
22	chr3:98838400-98846800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr3:98838800-98840200	Weak transcription	Osteobl	bone
24	chr3:98838800-98847000	Weak transcription	NH-A	brain
25	chr3:98839400-98846800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr3:98839400-98846800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr3:98842600-98845000	Weak transcription	Osteobl	bone
28	chr3:98843800-98846000	Enhancers	HSMMtube	muscle
29	chr3:98844200-98845000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr3:98844400-98846000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr3:98844600-98845800	Enhancers	Muscle Satellite Cultured Cells	--
32	chr3:98844600-98851200	Enhancers	HSMM	muscle
33	chr3:98845000-98845200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr3:98845000-98845400	Enhancers	HMEC	breast
35	chr3:98845000-98845400	Enhancers	NHLF	lung
36	chr3:98845000-98845600	Enhancers	Osteobl	bone
37	chr3:98845200-98845400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr3:98845400-98845600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr3:98845400-98846800	Weak transcription	HMEC	breast
40	chr3:98845400-98847000	Weak transcription	NHLF	lung
41	chr3:98845600-98847000	Weak transcription	Osteobl	bone
42	chr3:98845600-98847600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr3:98845800-98846800	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr3:98846000-98847000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr3:98846000-98847200	Weak transcription	HSMMtube	muscle
46	chr3:98846800-98847600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr3:98846800-98848000	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr3:98846800-98848400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr3:98846800-98849000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr3:98846800-98849000	Enhancers	Muscle Satellite Cultured Cells	--

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