Variant report

Variant	nsv1008563
Chromosome Location	chr3:137776151-137801394
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:536)
CpG islands
(count:183)
Chromatin interactive
region (count:29)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:536 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:137785097-137785621	GM12878	blood:	n/a	n/a
2	ATF2	chr3:137785134-137785566	GM12878	blood:	n/a	n/a
3	ATF3	chr3:137787378-137787793	A549	lung:	n/a	n/a
4	BACH1	chr3:137791661-137791861	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:137787433-137787783	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr3:137785253-137785567	GM12878	blood:	n/a	n/a
7	BATF	chr3:137785171-137785600	GM12878	blood:	n/a	n/a
8	BCL11A	chr3:137785184-137785605	GM12878	blood:	n/a	n/a
9	BCL3	chr3:137797771-137798329	A549	lung:	n/a	n/a
10	BHLHE40	chr3:137787456-137787761	K562	blood:	n/a	chr3:137787472-137787488
11	BHLHE40	chr3:137778054-137778112	GM12878	blood:	n/a	n/a
12	BHLHE40	chr3:137787441-137787777	GM12878	blood:	n/a	chr3:137787472-137787488
13	BHLHE40	chr3:137801377-137801613	K562	blood:	n/a	n/a
14	BRCA1	chr3:137787458-137787700	HepG2	liver:	n/a	n/a
15	BRCA1	chr3:137801277-137801693	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr3:137798000-137798310	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr3:137801226-137801812	HCT-116	colon:	n/a	n/a
18	CEBPB	chr3:137797808-137798324	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr3:137797630-137798331	IMR90	lung:	n/a	n/a
20	CEBPB	chr3:137800574-137802165	IMR90	lung:	n/a	chr3:137801266-137801278
21	CEBPB	chr3:137796837-137797381	A549	lung:	n/a	chr3:137797112-137797124
22	CEBPB	chr3:137796965-137797279	A549	lung:	n/a	chr3:137797112-137797124
23	CEBPB	chr3:137797673-137798389	A549	lung:	n/a	n/a
24	CEBPB	chr3:137796967-137797295	A549	lung:	n/a	chr3:137797112-137797124
25	CEBPB	chr3:137797865-137798275	MCF-7	breast:	n/a	n/a
26	CEBPB	chr3:137797891-137798249	A549	lung:	n/a	n/a
27	CEBPB	chr3:137797730-137798314	A549	lung:	n/a	n/a
28	CEBPB	chr3:137796946-137797290	IMR90	lung:	n/a	chr3:137797112-137797124
29	CEBPB	chr3:137801254-137801901	Hela-S3	cervix:	n/a	chr3:137801266-137801278
30	CEBPB	chr3:137787485-137787727	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr3:137797768-137798466	HCT-116	colon:	n/a	n/a
32	CHD1	chr3:137787483-137787730	GM12878	blood:	n/a	n/a
33	CHD2	chr3:137787481-137787754	GM12878	blood:	n/a	n/a
34	CHD2	chr3:137787565-137787755	HepG2	liver:	n/a	n/a
35	CHD2	chr3:137787435-137787776	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr3:137801372-137801724	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr3:137787461-137787792	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr3:137785126-137785627	GM12878	blood:	n/a	n/a
39	CTCF	chr3:137787540-137787690	BE2_C	brain:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
40	CTCF	chr3:137787520-137787670	HL-60	blood:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
41	CTCF	chr3:137787428-137787751	SK-N-SH_RA	brain:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
42	CTCF	chr3:137787160-137787310	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr3:137787185-137788047	A549	lung:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
44	CTCF	chr3:137787560-137787710	HRE	kidney:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
45	CTCF	chr3:137787540-137787690	NHDF-neo	bronchial:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
46	CTCF	chr3:137787428-137787767	GM10266	blood:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
47	CTCF	chr3:137787540-137787690	GM12873	blood:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
48	CTCF	chr3:137787500-137787650	RPTEC	kidney:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
49	CTCF	chr3:137787443-137787754	MCF-7	breast:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
50	CTCF	chr3:137787100-137787250	NHEK	skin:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:137787902-137787952	SK-N-MC	brain:	n/a
2	chr3:137787060-137787110	GM12878	blood:	n/a
3	chr3:137787902-137787952	Caco-2	colon:	n/a
4	chr3:137781206-137781256	SAEC	small airway:	n/a
5	chr3:137787060-137787110	AoSMC	blood vessel:	n/a
6	chr3:137781206-137781256	HRE	kidney:	n/a
7	chr3:137787060-137787110	HRPEpiC	eye:	n/a
8	chr3:137787060-137787110	AG09319	gingival:	n/a
9	chr3:137781206-137781256	H1-hESC	embryonic stem cell:	embryo
10	chr3:137787902-137787952	SAEC	small airway:	n/a
11	chr3:137787060-137787110	PANC-1	pancreas:	n/a
12	chr3:137787902-137787952	SKMC	muscle:	n/a
13	chr3:137787902-137787952	BJ	skin:	n/a
14	chr3:137781206-137781256	HNPCEpiC	eye:	n/a
15	chr3:137781206-137781256	BJ	skin:	n/a
16	chr3:137787060-137787110	HCM	heart:	n/a
17	chr3:137787902-137787952	MCF-7	breast:	n/a
18	chr3:137781206-137781256	CMK	blood:	n/a
19	chr3:137781206-137781256	AG09309	skin:	n/a
20	chr3:137781206-137781256	AG10803	skin:	n/a
21	chr3:137787060-137787110	GM12892	blood:	n/a
22	chr3:137787060-137787110	NH-A	brain:	n/a
23	chr3:137787060-137787110	HMEC	breast:	n/a
24	chr3:137787902-137787952	BE2_C	brain:	n/a
25	chr3:137781206-137781256	BE2_C	brain:	n/a
26	chr3:137787902-137787952	AG09309	skin:	n/a
27	chr3:137781206-137781256	HCF	heart:	n/a
28	chr3:137787060-137787110	PrEC	prostate:	n/a
29	chr3:137787902-137787952	HCPEpiC	choroid plexus:	n/a
30	chr3:137781206-137781256	NH-A	brain:	n/a
31	chr3:137781206-137781256	NHDF-neo	bronchial:	n/a
32	chr3:137781206-137781256	HCPEpiC	choroid plexus:	n/a
33	chr3:137781206-137781256	U87	brain:	n/a
34	chr3:137787902-137787952	HL-60	blood:	n/a
35	chr3:137781206-137781256	Hela-S3	cervix:	n/a
36	chr3:137787902-137787952	CMK	blood:	n/a
37	chr3:137787902-137787952	GM19239	blood:	n/a
38	chr3:137787902-137787952	HPAEpiC	pulmonary alveolar:	n/a
39	chr3:137787060-137787110	CMK	blood:	n/a
40	chr3:137787902-137787952	GM06990	blood:	n/a
41	chr3:137787902-137787952	IMR90	lung:	fetal
42	chr3:137787902-137787952	HMEC	breast:	n/a
43	chr3:137787902-137787952	PFSK-1	brain:	n/a
44	chr3:137781206-137781256	A549	lung:	n/a
45	chr3:137787902-137787952	HNPCEpiC	eye:	n/a
46	chr3:137787060-137787110	ECC-1	luminal epithelium:	n/a
47	chr3:137787060-137787110	BE2_C	brain:	n/a
48	chr3:137787060-137787110	LNCaP	prostate:	n/a
49	chr3:137787902-137787952	HCF	heart:	n/a
50	chr3:137781206-137781256	NHBE	bronchial:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:137795704..137798653-chr3:137818142..137820266,2	K562	blood:
2	chr3:137787348..137788077-chr3:137837494..137838376,4	K562	blood:
3	chr3:137783378..137785801-chr3:137789498..137791513,2	K562	blood:
4	chr3:137776797..137779428-chr3:137782269..137783995,2	MCF-7	breast:
5	chr12:90428505..90430564-chr3:137781378..137783907,2	MCF-7	breast:
6	chr3:137787211..137788408-chr3:137837411..137838466,26	MCF-7	breast:
7	chr3:137786807..137788879-chr3:137836537..137838505,22	MCF-7	breast:
8	chr3:137798158..137800063-chr3:137800310..137802167,2	MCF-7	breast:
9	chr3:137787960..137791501-chr3:137797864..137801137,4	K562	blood:
10	chr3:137787535..137788103-chr3:138634909..138635442,2	K562	blood:
11	chr3:137779026..137781498-chr3:137783755..137785265,2	K562	blood:
12	chr3:137776797..137779428-chr3:137782269..137783995,2	MCF-7	breast:
13	chr3:137797953..137799816-chr3:137805788..137808409,2	MCF-7	breast:
14	chr3:137783065..137785092-chr3:137890925..137893820,2	MCF-7	breast:
15	chr3:137774393..137777110-chr3:137777951..137779797,2	K562	blood:
16	chr3:137781336..137783358-chr3:137787171..137788980,2	MCF-7	breast:
17	chr3:137781336..137783358-chr3:137787171..137788980,2	MCF-7	breast:
18	chr3:137787960..137790369-chr3:137798612..137800700,2	K562	blood:
19	chr3:137780995..137783087-chr3:137786062..137788578,2	MCF-7	breast:
20	chr3:137795070..137797856-chr3:137805408..137807844,2	K562	blood:
21	chr3:137798306..137800637-chr3:137905206..137907659,2	MCF-7	breast:
22	chr3:137774393..137777110-chr3:137777951..137779797,2	K562	blood:
23	chr3:137796613..137798345-chr3:137800057..137802193,2	MCF-7	breast:
24	chr3:137779026..137781498-chr3:137783755..137785265,2	K562	blood:
25	chr3:137748327..137751099-chr3:137781297..137783702,2	MCF-7	breast:
26	chr3:137787702..137789743-chr3:137892211..137893755,2	MCF-7	breast:
27	chr3:137783378..137785801-chr3:137789498..137791513,2	K562	blood:
28	chr3:137789176..137789822-chr3:137837460..137838165,2	MCF-7	breast:
29	chr3:137794586..137797372-chr3:137799384..137801141,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-A4GNT-3	chr3:137799191-137799462	NONHSAT092319
2	lnc-A4GNT-3	chr3:137800576-137800671	NONHSAT092319

No data

Variant related genes	Relation type
DZIP1L	TF binding region
DZIP1L	CpG island
ENSG00000114098	chromatin interactions
ENSG00000158163	chromatin interactions
ENSG00000138231	chromatin interactions

Extended variants
information (count: 993 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:993 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564236965	chr3:137776155-137776156	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs148436089	chr3:137776177-137776178	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs142508326	chr3:137776208-137776209	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186658933	chr3:137776220-137776221	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs576623850	chr3:137776224-137776225	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150941279	chr3:137776242-137776243	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs9813719	chr3:137776265-137776266	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs568479062	chr3:137776271-137776272	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs34947108	chr3:137776314-137776315	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs191451714	chr3:137776363-137776364	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550924087	chr3:137776368-137776369	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571059929	chr3:137776373-137776374	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540098172	chr3:137776408-137776409	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116488973	chr3:137776457-137776458	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140308709	chr3:137776530-137776531	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs436145	chr3:137776539-137776540	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs572144298	chr3:137776550-137776551	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540505456	chr3:137776607-137776608	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565274362	chr3:137776623-137776624	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs575262751	chr3:137776676-137776677	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541356135	chr3:137776682-137776683	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532560920	chr3:137776696-137776697	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs405517	chr3:137776701-137776702	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs28452023	chr3:137776720-137776721	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373768619	chr3:137776781-137776782	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs577903115	chr3:137776826-137776827	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs112841865	chr3:137776861-137776862	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs559945673	chr3:137776877-137776878	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs573487904	chr3:137776918-137776919	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs529723684	chr3:137776920-137776921	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181573091	chr3:137776937-137776938	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530987783	chr3:137776938-137776939	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550707960	chr3:137777019-137777020	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs564496137	chr3:137777041-137777042	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs1825081	chr3:137777065-137777066	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs143386505	chr3:137777110-137777111	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs3084349	chr3:137777129-137777130	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs368735793	chr3:137777130-137777131	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs547291704	chr3:137777133-137777134	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs567103160	chr3:137777143-137777144	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs536069941	chr3:137777176-137777177	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544344900	chr3:137777227-137777228	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549525581	chr3:137777262-137777263	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs115591307	chr3:137777292-137777293	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs537903182	chr3:137777348-137777349	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs72991154	chr3:137777463-137777464	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs186066762	chr3:137777509-137777510	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs533870906	chr3:137777517-137777518	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190869917	chr3:137777564-137777565	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs114992518	chr3:137777571-137777572	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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	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
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	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
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Schizophrenia	18511947	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
abnormal development	18461090	CNVD

Chromatin state (count:757 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:137729400-137780400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:137742000-137780200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr3:137744400-137792000	Weak transcription	Fetal Kidney	kidney
4	chr3:137749600-137780000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr3:137750000-137781800	Weak transcription	Lung	lung
6	chr3:137750600-137782200	Weak transcription	Fetal Intestine Small	intestine
7	chr3:137754400-137783000	Weak transcription	Stomach Mucosa	stomach
8	chr3:137763000-137780600	Weak transcription	Fetal Muscle Leg	muscle
9	chr3:137763000-137797600	Weak transcription	Hela-S3	cervix
10	chr3:137763400-137780400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr3:137763400-137781400	Weak transcription	HSMMtube	muscle
12	chr3:137763400-137782600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr3:137763600-137778200	Weak transcription	HSMM	muscle
14	chr3:137766200-137781000	Weak transcription	NHEK	skin
15	chr3:137766800-137780400	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr3:137766800-137783600	Weak transcription	Brain Substantia Nigra	brain
17	chr3:137767000-137778800	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr3:137767000-137782800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr3:137767200-137791800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr3:137767400-137780400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr3:137767400-137780400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr3:137767600-137779600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr3:137768200-137777400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr3:137768200-137780000	Weak transcription	Spleen	Spleen
25	chr3:137768200-137782800	Weak transcription	Esophagus	oesophagus
26	chr3:137768200-137787600	Weak transcription	A549	lung
27	chr3:137768400-137777800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr3:137768400-137780400	Weak transcription	Stomach Smooth Muscle	stomach
29	chr3:137768400-137782200	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr3:137768600-137780000	Weak transcription	Aorta	Aorta
31	chr3:137768600-137782200	Weak transcription	Gastric	stomach
32	chr3:137768600-137783600	Weak transcription	Pancreas	Pancrea
33	chr3:137768800-137778200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr3:137768800-137778200	Weak transcription	Left Ventricle	heart
35	chr3:137768800-137778800	Weak transcription	Fetal Stomach	stomach
36	chr3:137768800-137779000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr3:137768800-137779600	Weak transcription	NHDF-Ad	bronchial
38	chr3:137768800-137779600	Weak transcription	Osteobl	bone
39	chr3:137768800-137779800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr3:137768800-137779800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr3:137768800-137779800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr3:137768800-137779800	Weak transcription	Right Ventricle	heart
43	chr3:137768800-137781000	Weak transcription	Rectal Smooth Muscle	rectum
44	chr3:137769000-137780000	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr3:137769400-137780400	Weak transcription	NHLF	lung
46	chr3:137769800-137785600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr3:137770200-137780200	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr3:137770200-137783600	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr3:137770400-137781200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr3:137770400-137783600	Weak transcription	Fetal Lung	lung

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