Variant report

Variant	nsv526089
Chromosome Location	chr3:138106698-138122781
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:321)
CpG islands
(count:183)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:321 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:138117981-138118405	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:138119682-138119990	HepG2	liver:	n/a	n/a
3	ATF3	chr3:138109096-138109544	A549	lung:	n/a	n/a
4	ATF3	chr3:138109014-138109666	HCT-116	colon:	n/a	n/a
5	BATF	chr3:138107966-138108138	GM12878	blood:	n/a	n/a
6	BHLHE40	chr3:138118065-138118395	HepG2	liver:	n/a	n/a
7	BHLHE40	chr3:138117959-138119029	HepG2	liver:	n/a	n/a
8	BHLHE40	chr3:138118625-138118951	HepG2	liver:	n/a	n/a
9	BRCA1	chr3:138109188-138109450	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr3:138108940-138109663	HCT-116	colon:	n/a	n/a
11	CEBPB	chr3:138119670-138120088	HepG2	liver:	n/a	n/a
12	CEBPB	chr3:138119716-138120054	HepG2	liver:	n/a	n/a
13	CEBPB	chr3:138108828-138109568	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr3:138109232-138109558	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr3:138108958-138109547	A549	lung:	n/a	n/a
16	CEBPB	chr3:138108830-138109582	IMR90	lung:	n/a	n/a
17	CEBPD	chr3:138118636-138118923	HepG2	liver:	n/a	n/a
18	CHD2	chr3:138118083-138118431	HepG2	liver:	n/a	n/a
19	CHD2	chr3:138109158-138109568	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr3:138120701-138120845	H1-hESC	embryonic stem cell:	n/a	n/a
21	CREB1	chr3:138117742-138118477	HepG2	liver:	n/a	n/a
22	CREB1	chr3:138117772-138118477	HepG2	liver:	n/a	n/a
23	CTCF	chr3:138116801-138117115	GM12878	blood:	n/a	chr3:138116949-138116967
24	CTCF	chr3:138116880-138117030	HA-sp	spinal cord:	n/a	chr3:138116949-138116967
25	CTCF	chr3:138115620-138115770	HepG2	liver:	n/a	n/a
26	CTCF	chr3:138116938-138116983	GM13976	blood:	n/a	chr3:138116949-138116967
27	CTCF	chr3:138116913-138117044	GM10266	blood:	n/a	chr3:138116949-138116967
28	CTCF	chr3:138116880-138117030	MCF-7	breast:	n/a	chr3:138116949-138116967
29	CTCF	chr3:138116883-138116971	LNCaP	prostate:	n/a	chr3:138116949-138116967
30	CTCF	chr3:138116900-138117050	HBMEC	blood vessel:	n/a	chr3:138116949-138116967
31	CTCF	chr3:138116820-138116970	RPTEC	kidney:	n/a	chr3:138116949-138116967
32	CTCF	chr3:138116900-138117050	WERI-Rb-1	eye:	n/a	chr3:138116949-138116967
33	CTCF	chr3:138115640-138115790	MCF-7	breast:	n/a	n/a
34	CTCF	chr3:138116900-138117050	GM12878	blood:	n/a	chr3:138116949-138116967
35	CTCF	chr3:138116800-138116950	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr3:138116880-138117030	AG04449	skin:	n/a	chr3:138116949-138116967
37	CTCF	chr3:138116851-138117070	Hela-S3	cervix:	n/a	chr3:138116949-138116967
38	CTCF	chr3:138116849-138117087	MCF-7	breast:	n/a	chr3:138116949-138116967
39	CTCF	chr3:138116860-138117010	GM12875	blood:	n/a	chr3:138116949-138116967
40	CTCF	chr3:138116962-138117001	GM10248	blood:	n/a	n/a
41	CTCF	chr3:138116900-138117050	GM12869	blood:	n/a	chr3:138116949-138116967
42	CTCF	chr3:138116880-138117030	HCPEpiC	choroid plexus:	n/a	chr3:138116949-138116967
43	CTCF	chr3:138115580-138115730	HL-60	blood:	n/a	n/a
44	CTCF	chr3:138115620-138115770	GM12867	blood:	n/a	n/a
45	CTCF	chr3:138116920-138117070	SAEC	small airway:	n/a	chr3:138116949-138116967
46	CTCF	chr3:138116871-138117085	MCF-7	breast:	n/a	chr3:138116949-138116967
47	CTCF	chr3:138115671-138115699	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr3:138116871-138117090	MCF-7	breast:	n/a	chr3:138116949-138116967
49	CTCF	chr3:138116860-138117010	HCFaa	heart:	n/a	chr3:138116949-138116967
50	CTCF	chr3:138116854-138117029	HepG2	liver:	n/a	chr3:138116949-138116967

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:138121287-138121337	PrEC	prostate:	n/a
2	chr3:138121287-138121337	HIPEpiC	eye:	n/a
3	chr3:138121287-138121337	HCT-116	colon:	n/a
4	chr3:138115973-138116023	HMEC	breast:	n/a
5	chr3:138109298-138109348	CMK	blood:	n/a
6	chr3:138115973-138116023	HCM	heart:	n/a
7	chr3:138115973-138116023	AG10803	skin:	n/a
8	chr3:138109298-138109348	HUVEC	blood vessel:	n/a
9	chr3:138109298-138109348	HCT-116	colon:	n/a
10	chr3:138121287-138121337	HAEpiC	amniotic membrane:	n/a
11	chr3:138109298-138109348	ovcar-3	ovarian:	n/a
12	chr3:138121287-138121337	SK-N-SH	brain:	n/a
13	chr3:138121287-138121337	HEEpiC	esophagus:	n/a
14	chr3:138109298-138109348	HepG2	liver:	n/a
15	chr3:138109298-138109348	MCF-7	breast:	n/a
16	chr3:138115973-138116023	CMK	blood:	n/a
17	chr3:138121287-138121337	NHDF-neo	bronchial:	n/a
18	chr3:138115973-138116023	PrEC	prostate:	n/a
19	chr3:138121287-138121337	SK-N-SH_RA	brain:	n/a
20	chr3:138121287-138121337	NH-A	brain:	n/a
21	chr3:138109298-138109348	A549	lung:	n/a
22	chr3:138109298-138109348	GM19239	blood:	n/a
23	chr3:138115973-138116023	HepG2	liver:	n/a
24	chr3:138115973-138116023	NT2-D1	testis:	n/a
25	chr3:138121287-138121337	A549	lung:	n/a
26	chr3:138121287-138121337	Hepatocyte	liver:	n/a
27	chr3:138115973-138116023	ProgFib	skin:	n/a
28	chr3:138121287-138121337	ProgFib	skin:	n/a
29	chr3:138109298-138109348	PrEC	prostate:	n/a
30	chr3:138109298-138109348	ProgFib	skin:	n/a
31	chr3:138115973-138116023	HPAEpiC	pulmonary alveolar:	n/a
32	chr3:138121287-138121337	HCM	heart:	n/a
33	chr3:138115973-138116023	Caco-2	colon:	n/a
34	chr3:138115973-138116023	LNCaP	prostate:	n/a
35	chr3:138115973-138116023	NHBE	bronchial:	n/a
36	chr3:138115973-138116023	GM12892	blood:	n/a
37	chr3:138115973-138116023	AG09319	gingival:	n/a
38	chr3:138115973-138116023	SAEC	small airway:	n/a
39	chr3:138121287-138121337	SAEC	small airway:	n/a
40	chr3:138121287-138121337	Caco-2	colon:	n/a
41	chr3:138121287-138121337	NB4	blood:	n/a
42	chr3:138115973-138116023	H1-hESC	embryonic stem cell:	embryo
43	chr3:138121287-138121337	ECC-1	luminal epithelium:	n/a
44	chr3:138109298-138109348	AG04450	lung:	fetal
45	chr3:138109298-138109348	U87	brain:	n/a
46	chr3:138115973-138116023	SK-N-MC	brain:	n/a
47	chr3:138115973-138116023	PFSK-1	brain:	n/a
48	chr3:138109298-138109348	NB4	blood:	n/a
49	chr3:138121287-138121337	SK-N-MC	brain:	n/a
50	chr3:138109298-138109348	MCF10A-Er-Src	breast:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:138108024..138110952-chr3:138113271..138115084,3	MCF-7	breast:
2	chr3:138112036..138114862-chr3:138120590..138122113,2	K562	blood:
3	chr3:138069326..138072318-chr3:138105183..138106708,2	K562	blood:
4	chr3:138112862..138116319-chr3:138116763..138120380,3	MCF-7	breast:
5	chr3:138099681..138102999-chr3:138104936..138107535,3	MCF-7	breast:
6	chr3:138112036..138114862-chr3:138120590..138122113,2	K562	blood:
7	chr3:138094416..138096515-chr3:138105748..138108016,2	MCF-7	breast:
8	chr3:138049031..138051913-chr3:138117150..138118923,2	MCF-7	breast:
9	chr3:138112677..138114319-chr3:138192057..138194447,2	MCF-7	breast:
10	chr3:138108024..138110952-chr3:138113271..138115084,3	MCF-7	breast:
11	chr3:138113362..138114985-chr3:138120209..138122090,2	K562	blood:
12	chr3:138108137..138110673-chr3:138113889..138116211,2	K562	blood:
13	chr3:138050301..138052204-chr3:138116487..138117341,9	MCF-7	breast:
14	chr3:138113362..138114985-chr3:138120209..138122090,2	K562	blood:
15	chr3:138108137..138110673-chr3:138113889..138116211,2	K562	blood:

No data

Variant related genes	Relation type
MRAS	TF binding region
MRAS	CpG island
ENSG00000158186	chromatin interactions
ENSG00000158220	chromatin interactions

Extended variants
information (count: 620 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:620 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1209710	chr3:138106698-138106699	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs571245150	chr3:138106720-138106721	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs78025880	chr3:138106762-138106763	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs74803651	chr3:138106808-138106809	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566741615	chr3:138106817-138106818	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189342689	chr3:138106860-138106861	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555627211	chr3:138106865-138106866	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs563196463	chr3:138106931-138106932	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575564191	chr3:138106933-138106934	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547456446	chr3:138106952-138106953	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140396539	chr3:138106964-138106965	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs34229518	chr3:138106968-138106969	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs79609026	chr3:138107012-138107013	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567362479	chr3:138107051-138107052	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560061179	chr3:138107077-138107078	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573896960	chr3:138107084-138107085	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs6789235	chr3:138107097-138107098	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs181924363	chr3:138107154-138107155	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138046015	chr3:138107206-138107207	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs140878983	chr3:138107217-138107218	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs187391244	chr3:138107278-138107279	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs527366338	chr3:138107279-138107280	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547481504	chr3:138107290-138107291	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191027508	chr3:138107307-138107308	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535634133	chr3:138107311-138107312	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549215890	chr3:138107312-138107313	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182690617	chr3:138107315-138107316	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186459758	chr3:138107316-138107317	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376274837	chr3:138107328-138107329	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144708490	chr3:138107412-138107413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571879248	chr3:138107494-138107495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs538897584	chr3:138107555-138107556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs534003622	chr3:138107563-138107564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs116778302	chr3:138107568-138107569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs4346503	chr3:138107597-138107598	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs541145270	chr3:138107628-138107629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542833173	chr3:138107715-138107716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs562681383	chr3:138107726-138107727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs372678089	chr3:138107744-138107745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs35025151	chr3:138107786-138107787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs540890941	chr3:138107808-138107809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545307714	chr3:138107837-138107838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs190169374	chr3:138107864-138107865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs182788101	chr3:138107865-138107866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534817946	chr3:138107871-138107872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs13082471	chr3:138107880-138107881	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs543203245	chr3:138107883-138107884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs58019324	chr3:138107896-138107897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563078708	chr3:138107921-138107922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs187383826	chr3:138107934-138107935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	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
Gastric cancer	22014070	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:484 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:138076000-138108200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr3:138081600-138108200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr3:138090400-138119400	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr3:138097600-138116000	Weak transcription	Aorta	Aorta
5	chr3:138097600-138116600	Weak transcription	Brain Germinal Matrix	brain
6	chr3:138101200-138115000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr3:138101400-138108000	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr3:138101400-138108400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr3:138101400-138123000	Weak transcription	Fetal Lung	lung
10	chr3:138101600-138107800	Weak transcription	Osteobl	bone
11	chr3:138101600-138108000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr3:138101600-138108200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr3:138101600-138108200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr3:138101600-138108200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr3:138101600-138120400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr3:138101800-138108000	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr3:138101800-138108200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr3:138101800-138108200	Weak transcription	Pancreas	Pancrea
19	chr3:138101800-138108400	Weak transcription	Fetal Muscle Leg	muscle
20	chr3:138101800-138108400	Weak transcription	Rectal Smooth Muscle	rectum
21	chr3:138101800-138108600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr3:138102000-138107000	Strong transcription	HSMM	muscle
23	chr3:138102000-138108200	Weak transcription	Esophagus	oesophagus
24	chr3:138102000-138108200	Weak transcription	Fetal Muscle Trunk	muscle
25	chr3:138102400-138108000	Weak transcription	Psoas Muscle	Psoas
26	chr3:138102600-138108000	Weak transcription	Colon Smooth Muscle	Colon
27	chr3:138102600-138108200	Weak transcription	Stomach Smooth Muscle	stomach
28	chr3:138102600-138109200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr3:138103000-138108000	Weak transcription	Ovary	ovary
30	chr3:138103200-138108000	Weak transcription	Brain Hippocampus Middle	brain
31	chr3:138103400-138108600	Weak transcription	NHEK	skin
32	chr3:138103600-138107400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr3:138103600-138108200	Weak transcription	HMEC	breast
34	chr3:138103800-138107600	Weak transcription	Brain Anterior Caudate	brain
35	chr3:138103800-138108000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr3:138103800-138108000	Weak transcription	Brain Cingulate Gyrus	brain
37	chr3:138103800-138108200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr3:138103800-138108200	Weak transcription	Lung	lung
39	chr3:138103800-138108600	Weak transcription	Brain Angular Gyrus	brain
40	chr3:138103800-138109200	Weak transcription	Brain Substantia Nigra	brain
41	chr3:138104400-138106800	Enhancers	Right Ventricle	heart
42	chr3:138104800-138108000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr3:138105000-138107000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr3:138105200-138106800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr3:138105200-138109000	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr3:138105400-138108400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr3:138105600-138107400	Strong transcription	HSMMtube	muscle
48	chr3:138106000-138107000	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr3:138106000-138108400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr3:138106000-138109400	Enhancers	Left Ventricle	heart

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