Variant report

Variant	nsv460865
Chromosome Location	chr3:139411031-139455326
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:139429092-139429424	HepG2	liver:	n/a	n/a
2	ATF1	chr3:139411788-139411826	K562	blood:	n/a	n/a
3	BACH1	chr3:139440212-139440356	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:139440219-139440343	K562	blood:	n/a	n/a
5	CEBPB	chr3:139442294-139442632	IMR90	lung:	n/a	chr3:139442475-139442486 chr3:139442474-139442487
6	CEBPB	chr3:139455088-139455309	A549	lung:	n/a	chr3:139455212-139455225 chr3:139455213-139455224
7	CEBPB	chr3:139455140-139455321	K562	blood:	n/a	chr3:139455212-139455225 chr3:139455213-139455224
8	CEBPB	chr3:139442357-139442604	HepG2	liver:	n/a	chr3:139442475-139442486 chr3:139442474-139442487
9	CEBPB	chr3:139442393-139442615	A549	lung:	n/a	chr3:139442475-139442486 chr3:139442474-139442487
10	CEBPB	chr3:139455062-139455391	HepG2	liver:	n/a	chr3:139455212-139455225 chr3:139455213-139455224
11	CTCF	chr3:139437400-139437550	HVMF	connective:	n/a	chr3:139437465-139437481 chr3:139437467-139437480 chr3:139437466-139437487 chr3:139437464-139437482
12	CTCF	chr3:139437420-139437570	AG09309	skin:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
13	CTCF	chr3:139437340-139437490	GM12867	blood:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
14	CTCF	chr3:139437355-139437578	Medullo	brain:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
15	CTCF	chr3:139437342-139437575	LNCaP	prostate:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
16	CTCF	chr3:139437340-139437574	ProgFib	skin:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
17	CTCF	chr3:139436800-139436950	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr3:139437346-139437572	Pancreas_OC	pancreas:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
19	CTCF	chr3:139418214-139418236	GM12878	blood:	n/a	n/a
20	CTCF	chr3:139437360-139437510	GM06990	blood:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
21	CTCF	chr3:139432000-139432150	GM12869	blood:	n/a	n/a
22	CTCF	chr3:139437400-139437550	HRPEpiC	eye:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
23	CTCF	chr3:139437320-139437470	HAc	cerebellar:	n/a	n/a
24	CTCF	chr3:139437380-139437530	HCT-116	colon:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
25	CTCF	chr3:139437400-139437550	NHEK	skin:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
26	CTCF	chr3:139437400-139437550	Caco-2	colon:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
27	CTCF	chr3:139417342-139417391	GM12878	blood:	n/a	n/a
28	CTCF	chr3:139437356-139437517	A549	lung:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
29	CTCF	chr3:139437380-139437530	Hela-S3	cervix:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
30	CTCF	chr3:139437307-139437611	MCF-7	breast:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
31	CTCF	chr3:139437400-139437550	HCPEpiC	choroid plexus:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
32	CTCF	chr3:139437380-139437530	HEK293	kidney:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
33	CTCF	chr3:139437400-139437550	HPAF	blood vessel:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
34	CTCF	chr3:139437400-139437550	AG10803	skin:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
35	CTCF	chr3:139437233-139437629	H1-hESC	embryonic stem cell:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
36	CTCF	chr3:139437400-139437550	AoAF	blood vessel:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
37	CTCF	chr3:139437420-139437570	HMEC	breast:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
38	CTCF	chr3:139437380-139437530	NHDF-neo	bronchial:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
39	CTCF	chr3:139454400-139454550	GM12868	blood:	n/a	n/a
40	CTCF	chr3:139437359-139437544	GM12878	blood:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
41	CTCF	chr3:139437310-139437610	HepG2	liver:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
42	CTCF	chr3:139437340-139437592	MCF-7	breast:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
43	CTCF	chr3:139437380-139437530	HFF	foreskin:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
44	CTCF	chr3:139437440-139437590	GM12864	blood:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
45	CTCF	chr3:139437440-139437590	BE2_C	brain:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
46	CTCF	chr3:139437400-139437550	AG04449	skin:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
47	CTCF	chr3:139437380-139437530	HepG2	liver:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
48	CTCF	chr3:139437380-139437530	SAEC	small airway:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
49	CTCF	chr3:139437400-139437550	HUVEC	blood vessel:	n/a	chr3:139437467-139437480 chr3:139437465-139437481 chr3:139437466-139437487 chr3:139437464-139437482
50	CTCF	chr3:139418080-139418230	HRPEpiC	eye:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:139440415-139440465	HCF	heart:	n/a
2	chr3:139440415-139440465	NHDF-neo	bronchial:	n/a
3	chr3:139440415-139440465	HCPEpiC	choroid plexus:	n/a
4	chr3:139440415-139440465	HIPEpiC	eye:	n/a
5	chr3:139440415-139440465	PANC-1	pancreas:	n/a
6	chr3:139440415-139440465	BE2_C	brain:	n/a
7	chr3:139440415-139440465	SAEC	small airway:	n/a
8	chr3:139440415-139440465	GM06990	blood:	n/a
9	chr3:139440415-139440465	AG04449	skin:	fetal
10	chr3:139440415-139440465	HMEC	breast:	n/a
11	chr3:139440415-139440465	HRCEpiC	kidney:	n/a
12	chr3:139440415-139440465	HAEpiC	amniotic membrane:	n/a
13	chr3:139440415-139440465	NB4	blood:	n/a
14	chr3:139440415-139440465	AoSMC	blood vessel:	n/a
15	chr3:139440415-139440465	HRE	kidney:	n/a
16	chr3:139440415-139440465	GM12878	blood:	n/a
17	chr3:139440415-139440465	CMK	blood:	n/a
18	chr3:139440415-139440465	HRPEpiC	eye:	n/a
19	chr3:139440415-139440465	SK-N-SH_RA	brain:	n/a
20	chr3:139440415-139440465	SK-N-SH	brain:	n/a
21	chr3:139440415-139440465	K562	blood:	n/a
22	chr3:139440415-139440465	Caco-2	colon:	n/a
23	chr3:139440415-139440465	HUVEC	blood vessel:	n/a
24	chr3:139440415-139440465	AG10803	skin:	n/a
25	chr3:139440415-139440465	GM19239	blood:	n/a
26	chr3:139440415-139440465	HNPCEpiC	eye:	n/a
27	chr3:139440415-139440465	NHBE	bronchial:	n/a
28	chr3:139440415-139440465	SKMC	muscle:	n/a
29	chr3:139440415-139440465	GM12891	blood:	n/a
30	chr3:139440415-139440465	HepG2	liver:	n/a
31	chr3:139440415-139440465	MCF-7	breast:	n/a
32	chr3:139440415-139440465	SK-N-MC	brain:	n/a
33	chr3:139440415-139440465	PrEC	prostate:	n/a
34	chr3:139440415-139440465	ProgFib	skin:	n/a
35	chr3:139440415-139440465	AG09309	skin:	n/a
36	chr3:139440415-139440465	Hela-S3	cervix:	n/a
37	chr3:139440415-139440465	RPTEC	kidney:	n/a
38	chr3:139440415-139440465	A549	lung:	n/a
39	chr3:139440415-139440465	Jurkat	blood:	n/a
40	chr3:139440415-139440465	U87	brain:	n/a
41	chr3:139440415-139440465	H1-hESC	embryonic stem cell:	embryo
42	chr3:139440415-139440465	HPAEpiC	pulmonary alveolar:	n/a
43	chr3:139440415-139440465	AG09319	gingival:	n/a
44	chr3:139440415-139440465	GM12892	blood:	n/a
45	chr3:139440415-139440465	BJ	skin:	n/a
46	chr3:139440415-139440465	Hepatocyte	liver:	n/a
47	chr3:139440415-139440465	ECC-1	luminal epithelium:	n/a
48	chr3:139440415-139440465	ovcar-3	ovarian:	n/a
49	chr3:139440415-139440465	IMR90	lung:	fetal
50	chr3:139440415-139440465	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:139454562..139456227-chr3:139456551..139459726,3	MCF-7	breast:
2	chr3:139436698..139437886-chr3:139769877..139770897,3	MCF-7	breast:
3	chr3:139439720..139442985-chr3:139448975..139450787,3	K562	blood:
4	chr3:139404630..139407387-chr3:139410965..139413960,2	MCF-7	breast:
5	chr3:139409787..139411878-chr3:139415425..139418176,2	MCF-7	breast:
6	chr3:139435753..139436447-chr3:139770298..139770858,2	MCF-7	breast:
7	chr3:139409787..139411878-chr3:139415425..139418176,2	MCF-7	breast:
8	chr3:139437070..139437910-chr3:139653098..139654016,8	MCF-7	breast:
9	chr12:116867357..116868122-chr3:139445836..139446358,2	MCF-7	breast:
10	chr3:139439720..139442985-chr3:139448975..139450787,3	K562	blood:
11	chr3:139404409..139407815-chr3:139408609..139412538,3	K562	blood:
12	chr3:139404964..139406658-chr3:139409631..139411232,2	K562	blood:
13	chr3:139437002..139437900-chr3:139652880..139654338,15	MCF-7	breast:
14	chr3:139438799..139439673-chr3:139652877..139653733,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000250543	TF binding region
ENSG00000250543	CpG island
ENSG00000158258	chromatin interactions

Extended variants
information (count: 1091 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1091 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11720063	chr3:139411031-139411032	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs546658460	chr3:139411102-139411103	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs368698302	chr3:139411113-139411114	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs199729384	chr3:139411192-139411193	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs560187215	chr3:139411195-139411196	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs528809780	chr3:139411210-139411211	Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs79478276	chr3:139411215-139411216	Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs200861017	chr3:139411216-139411217	Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs537221318	chr3:139411317-139411318	Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs11720232	chr3:139411320-139411321	Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs62273122	chr3:139411322-139411323	Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs539539357	chr3:139411350-139411351	Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs552998787	chr3:139411351-139411352	Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs572883522	chr3:139411368-139411369	Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs535754760	chr3:139411382-139411383	Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs11720212	chr3:139411403-139411404	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs575397644	chr3:139411426-139411427	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs550681430	chr3:139411461-139411462	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs75010581	chr3:139411472-139411473	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs73220996	chr3:139411552-139411553	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs181747423	chr3:139411572-139411573	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs144176952	chr3:139411576-139411577	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs376684705	chr3:139411583-139411584	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs367687990	chr3:139411638-139411639	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs540309232	chr3:139411774-139411775	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs560225872	chr3:139411830-139411831	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs528849667	chr3:139411849-139411850	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs542533114	chr3:139411935-139411936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7641383	chr3:139411959-139411960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs116303417	chr3:139411984-139411985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533257518	chr3:139411992-139411993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs35704270	chr3:139412013-139412014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546964473	chr3:139412032-139412033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570711171	chr3:139412070-139412071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533282372	chr3:139412108-139412109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546651917	chr3:139412109-139412110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs566878220	chr3:139412118-139412119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535433031	chr3:139412123-139412124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555642417	chr3:139412208-139412209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369477445	chr3:139412283-139412284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs79644584	chr3:139412339-139412340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186267028	chr3:139412340-139412341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558011172	chr3:139412358-139412359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577896528	chr3:139412461-139412462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs141087183	chr3:139412478-139412479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs78216086	chr3:139412508-139412509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191010574	chr3:139412515-139412516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566624921	chr3:139412523-139412524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs55983509	chr3:139412533-139412534	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs182725247	chr3:139412547-139412548	Weak 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
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
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:139409000-139417800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr3:139409800-139411200	Enhancers	Fetal Heart	heart
3	chr3:139409800-139413400	Weak transcription	Brain Germinal Matrix	brain
4	chr3:139411200-139411400	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr3:139411200-139414000	Weak transcription	Fetal Heart	heart
6	chr3:139412400-139412800	Enhancers	Pancreas	Pancrea
7	chr3:139413400-139413600	Enhancers	Brain Germinal Matrix	brain
8	chr3:139413400-139414400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr3:139413600-139414000	Weak transcription	Brain Germinal Matrix	brain
10	chr3:139413800-139414400	Enhancers	Adipose Nuclei	Adipose
11	chr3:139413800-139414400	Enhancers	Fetal Brain Male	brain
12	chr3:139414000-139414800	Enhancers	H1 Cell Line	embryonic stem cell
13	chr3:139414000-139414800	Enhancers	Brain Germinal Matrix	brain
14	chr3:139414000-139414800	Enhancers	Fetal Heart	heart
15	chr3:139414000-139415000	Enhancers	Fetal Brain Female	brain
16	chr3:139414000-139415200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr3:139414200-139414800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr3:139414200-139415200	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr3:139414400-139415400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr3:139415400-139416200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr3:139416200-139416800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr3:139417800-139418400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr3:139423000-139423200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr3:139423200-139433800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr3:139423600-139425600	Enhancers	Fetal Brain Male	brain
26	chr3:139424400-139425800	Enhancers	Fetal Brain Female	brain
27	chr3:139425600-139426600	Weak transcription	Fetal Brain Male	brain
28	chr3:139426600-139428000	Enhancers	Fetal Brain Male	brain
29	chr3:139428400-139429600	Enhancers	Psoas Muscle	Psoas
30	chr3:139428400-139430000	Enhancers	HepG2	liver
31	chr3:139429000-139429400	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr3:139429200-139429800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr3:139430000-139433400	Weak transcription	HepG2	liver
34	chr3:139433200-139436000	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr3:139433400-139433600	Enhancers	HepG2	liver
36	chr3:139433600-139434600	Weak transcription	HepG2	liver
37	chr3:139433600-139435400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr3:139433600-139435600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr3:139433600-139435600	Enhancers	HMEC	breast
40	chr3:139433600-139435600	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr3:139433600-139435800	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr3:139433800-139435400	Enhancers	NHEK	skin
43	chr3:139434000-139437200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr3:139434400-139435200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr3:139434600-139437400	Enhancers	HepG2	liver
46	chr3:139434600-139437800	Enhancers	HSMMtube	muscle
47	chr3:139435400-139435600	Enhancers	Right Ventricle	heart
48	chr3:139435400-139437400	Enhancers	Ovary	ovary
49	chr3:139435400-139437800	Enhancers	Fetal Stomach	stomach
50	chr3:139435800-139436400	Enhancers	Fetal Lung	lung

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