Variant report

Variant	nsv1008375
Chromosome Location	chr1:113028271-113060221
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:666)
CpG islands
(count:1526)
Chromatin interactive
region (count:36)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:666 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:113057939-113058182	K562	blood:	n/a	n/a
2	ATF2	chr1:113051104-113051472	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:113051209-113051411	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:113044464-113044972	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:113043744-113043795	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr1:113051210-113051267	K562	blood:	n/a	n/a
7	BHLHE40	chr1:113051132-113051484	GM12878	blood:	n/a	n/a
8	BRCA1	chr1:113051162-113051356	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr1:113058196-113058225	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr1:113044627-113044628	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr1:113044600-113044646	HepG2	liver:	n/a	n/a
12	CCNT2	chr1:113044610-113045036	K562	blood:	n/a	chr1:113044699-113044708
13	CEBPB	chr1:113044494-113044521	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr1:113030434-113030556	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:113030462-113030551	K562	blood:	n/a	n/a
16	CEBPB	chr1:113032141-113032433	HepG2	liver:	n/a	n/a
17	CEBPB	chr1:113042376-113042517	HepG2	liver:	n/a	n/a
18	CEBPB	chr1:113057721-113057847	IMR90	lung:	n/a	n/a
19	CEBPB	chr1:113030352-113030659	IMR90	lung:	n/a	n/a
20	CEBPB	chr1:113030460-113030555	Hela-S3	cervix:	n/a	n/a
21	CHD1	chr1:113044683-113044699	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr1:113050626-113050657	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr1:113051134-113051503	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr1:113051038-113051040	HepG2	liver:	n/a	n/a
25	CHD2	chr1:113044771-113044843	HepG2	liver:	n/a	n/a
26	CHD2	chr1:113051261-113051354	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr1:113051056-113051411	GM12878	blood:	n/a	n/a
28	CREB1	chr1:113051205-113051441	A549	lung:	n/a	n/a
29	CREB1	chr1:113051086-113051591	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTBP2	chr1:113049984-113052188	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTBP2	chr1:113044363-113045301	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr1:113044560-113044710	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr1:113044450-113044741	MCF-7	breast:	n/a	n/a
34	CTCF	chr1:113051225-113051423	GM19238	blood:	n/a	chr1:113051361-113051374
35	CTCF	chr1:113060100-113060250	HMEC	breast:	n/a	n/a
36	CTCF	chr1:113044540-113044690	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr1:113044479-113044750	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr1:113051280-113051430	GM12865	blood:	n/a	chr1:113051361-113051374
39	CTCF	chr1:113043720-113043870	K562	blood:	n/a	n/a
40	CTCF	chr1:113044520-113044670	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:113051304-113051390	Pancreas_OC	pancreas:	n/a	chr1:113051361-113051374
42	CTCF	chr1:113051240-113051390	SAEC	small airway:	n/a	chr1:113051361-113051374
43	CTCF	chr1:113044475-113044740	MCF-7	breast:	n/a	n/a
44	CTCF	chr1:113044500-113044650	WI-38	lung:	n/a	n/a
45	CTCF	chr1:113044540-113044690	BJ	skin:	n/a	n/a
46	CTCF	chr1:113051220-113051370	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr1:113051321-113051385	ProgFib	skin:	n/a	chr1:113051361-113051374
48	CTCF	chr1:113044500-113044650	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr1:113044520-113044670	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr1:113044455-113044774	GM19240	blood:	n/a	n/a

(count:1526 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:113057647-113057697	HNPCEpiC	eye:	n/a
2	chr1:113057647-113057697	HNPCEpiC	eye:	n/a
3	chr1:113056151-113056201	HRPEpiC	eye:	n/a
4	chr1:113033507-113033557	Hepatocyte	liver:	n/a
5	chr1:113042739-113042789	HAEpiC	amniotic membrane:	n/a
6	chr1:113041557-113041607	U87	brain:	n/a
7	chr1:113052167-113052217	HUVEC	blood vessel:	n/a
8	chr1:113044437-113044487	ProgFib	skin:	n/a
9	chr1:113033507-113033557	SK-N-MC	brain:	n/a
10	chr1:113051139-113051189	HCT-116	colon:	n/a
11	chr1:113044437-113044487	HNPCEpiC	eye:	n/a
12	chr1:113051090-113051140	NHDF-neo	bronchial:	n/a
13	chr1:113052563-113052613	HCF	heart:	n/a
14	chr1:113051171-113051221	GM12878	blood:	n/a
15	chr1:113051353-113051403	K562	blood:	n/a
16	chr1:113051777-113051827	NH-A	brain:	n/a
17	chr1:113033507-113033557	AG10803	skin:	n/a
18	chr1:113052563-113052613	AG09309	skin:	n/a
19	chr1:113044437-113044487	HMEC	breast:	n/a
20	chr1:113057647-113057697	AG09319	gingival:	n/a
21	chr1:113042739-113042789	PFSK-1	brain:	n/a
22	chr1:113051777-113051827	NHBE	bronchial:	n/a
23	chr1:113056151-113056201	RPTEC	kidney:	n/a
24	chr1:113051846-113051896	ProgFib	skin:	n/a
25	chr1:113051171-113051221	HAEpiC	amniotic membrane:	n/a
26	chr1:113041557-113041607	SK-N-SH	brain:	n/a
27	chr1:113042739-113042789	K562	blood:	n/a
28	chr1:113051777-113051827	ovcar-3	ovarian:	n/a
29	chr1:113051315-113051365	HCPEpiC	choroid plexus:	n/a
30	chr1:113042739-113042789	Caco-2	colon:	n/a
31	chr1:113051043-113051093	SAEC	small airway:	n/a
32	chr1:113033507-113033557	ProgFib	skin:	n/a
33	chr1:113047945-113047995	NHDF-neo	bronchial:	n/a
34	chr1:113050814-113050864	HL-60	blood:	n/a
35	chr1:113051171-113051221	RPTEC	kidney:	n/a
36	chr1:113050814-113050864	HRCEpiC	kidney:	n/a
37	chr1:113042739-113042789	HNPCEpiC	eye:	n/a
38	chr1:113050539-113050589	GM12892	blood:	n/a
39	chr1:113051777-113051827	AG10803	skin:	n/a
40	chr1:113044860-113044910	HEEpiC	esophagus:	n/a
41	chr1:113050814-113050864	BE2_C	brain:	n/a
42	chr1:113050539-113050589	HepG2	liver:	n/a
43	chr1:113051171-113051221	T-47D	breast:	n/a
44	chr1:113052563-113052613	K562	blood:	n/a
45	chr1:113047945-113047995	AG04450	lung:	fetal
46	chr1:113041557-113041607	AG09309	skin:	n/a
47	chr1:113045271-113045321	BJ	skin:	n/a
48	chr1:113052167-113052217	AG09309	skin:	n/a
49	chr1:113045271-113045321	Caco-2	colon:	n/a
50	chr1:113052167-113052217	HepG2	liver:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:113050916..113052536-chr1:113056260..113057826,2	K562	blood:
2	chr1:112937399..112939003-chr1:113054969..113056954,2	MCF-7	breast:
3	chr1:113043596..113046525-chr1:113046998..113048803,2	K562	blood:
4	chr1:113044372..113046496-chr1:113155425..113157042,2	K562	blood:
5	chr1:113043050..113044804-chr1:113159767..113162652,3	MCF-7	breast:
6	chr1:113038256..113040646-chr1:113160128..113161834,2	MCF-7	breast:
7	chr1:113034961..113036793-chr1:113158918..113161759,2	K562	blood:
8	chr1:113041409..113044324-chr1:113246115..113248813,2	MCF-7	breast:
9	chr1:113044125..113045114-chr1:113156151..113157755,13	MCF-7	breast:
10	chr1:113046413..113048318-chr1:113249191..113251337,2	MCF-7	breast:
11	chr1:113053649..113055695-chr1:113241407..113243136,2	K562	blood:
12	chr1:113051455..113054966-chr1:113056475..113060104,3	MCF-7	breast:
13	chr1:113044204..113044716-chr1:113249848..113250491,2	MCF-7	breast:
14	chr1:113050070..113052532-chr1:113159337..113161675,2	MCF-7	breast:
15	chr1:113042549..113044879-chr1:113047286..113049813,2	MCF-7	breast:
16	chr1:113043596..113046525-chr1:113046998..113048803,2	K562	blood:
17	chr1:113057544..113060149-chr1:113196498..113199134,2	K562	blood:
18	chr1:113057899..113060192-chr1:113160465..113162530,2	MCF-7	breast:
19	chr1:113048065..113050562-chr1:113256191..113259414,3	MCF-7	breast:
20	chr1:113044915..113046435-chr1:113049635..113052244,3	K562	blood:
21	chr1:113038165..113040029-chr1:113043903..113046113,2	MCF-7	breast:
22	chr1:113038165..113040029-chr1:113043903..113046113,2	MCF-7	breast:
23	chr1:113046634..113048206-chr1:113160443..113162083,2	MCF-7	breast:
24	chr1:113050916..113052536-chr1:113056260..113057826,2	K562	blood:
25	chr1:113044938..113047798-chr1:113154347..113157279,3	MCF-7	breast:
26	chr1:113044387..113046932-chr1:113047303..113049835,3	K562	blood:
27	chr1:113042549..113044879-chr1:113047286..113049813,2	MCF-7	breast:
28	chr1:113042799..113045206-chr1:113056989..113060717,3	MCF-7	breast:
29	chr1:113059419..113061818-chr1:113160250..113161994,2	MCF-7	breast:
30	chr1:113044160..113045084-chr1:113249254..113250612,4	K562	blood:
31	chr1:113053258..113055489-chr1:113072240..113074967,2	MCF-7	breast:
32	chr1:113044387..113046932-chr1:113047303..113049835,3	K562	blood:
33	chr1:112933243..112934045-chr1:113044555..113045071,2	K562	blood:
34	chr1:113044927..113047508-chr1:113050744..113052347,2	K562	blood:
35	chr1:113043664..113046316-chr1:113246773..113250102,3	K562	blood:
36	chr1:112912009..112912593-chr1:113044548..113045085,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTTNBP2NL-5	chr1:113045651-113046522	predAs_chen_BX119273_1
2	lnc-CTTNBP2NL-4	chr1:113041688-113042948	NONHSAT005235

No data

Variant related genes	Relation type
WNT2B	TF binding region
WNT2B	CpG island
ENSG00000261595	chromatin interactions
ENSG00000155366	chromatin interactions
ENSG00000143079	chromatin interactions
ENSG00000116489	chromatin interactions
ENSG00000134245	chromatin interactions
ENSG00000155367	chromatin interactions
ENSG00000155363	chromatin interactions
ENSG00000007341	chromatin interactions

Extended variants
information (count: 1083 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:1083 , 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	rs142550467	chr1:113029463-113029464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs149843596	chr1:113029466-113029467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs188348107	chr1:113029514-113029515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115222302	chr1:113029530-113029531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs533595089	chr1:113029532-113029533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs553716957	chr1:113029568-113029569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs57837199	chr1:113029631-113029632	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs545668444	chr1:113029652-113029653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs556009909	chr1:113029714-113029715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575846069	chr1:113029724-113029725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs541584098	chr1:113029751-113029752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561228707	chr1:113029753-113029754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs180765455	chr1:113029756-113029757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556050006	chr1:113030608-113030609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575885453	chr1:113030615-113030616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs181181958	chr1:113030637-113030638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555522012	chr1:113030687-113030688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs61820471	chr1:113030791-113030792	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs540741328	chr1:113030806-113030807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560348267	chr1:113030824-113030825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs186977781	chr1:113030828-113030829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs546170067	chr1:113030852-113030853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191414019	chr1:113030875-113030876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559533858	chr1:113030929-113030930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs71584739	chr1:113030930-113030931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572294006	chr1:113030943-113030944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs377277070	chr1:113030944-113030945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs72699044	chr1:113030985-113030986	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs548537267	chr1:113030986-113030987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs576894733	chr1:113031848-113031849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs57706772	chr1:113031851-113031852	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs549865542	chr1:113031852-113031853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs77328765	chr1:113031898-113031899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs139436289	chr1:113031900-113031901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs539921106	chr1:113031981-113031982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs201549284	chr1:113032027-113032028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556669043	chr1:113032042-113032043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2488784	chr1:113032116-113032117	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs150063122	chr1:113032144-113032145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs368708237	chr1:113032145-113032146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs7525280	chr1:113032167-113032168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs552991933	chr1:113032182-113032183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530365479	chr1:113032292-113032293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs572647439	chr1:113032363-113032364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs35427726	chr1:113032404-113032405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs397751669	chr1:113032414-113032415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs200688054	chr1:113032415-113032416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs201935747	chr1:113032416-113032417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs541267661	chr1:113032456-113032457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs564317825	chr1:113032481-113032482	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Asthma	20841430	CNVD
Aetanephric adenomas	20802469	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	21956041	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	16573809	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Breast cancer	17899364	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Melanoma	19671679	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1070 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:113029400-113029800	Enhancers	Monocytes-CD14+_RO01746	blood
2	chr1:113030600-113031000	Enhancers	Placenta	Placenta
3	chr1:113031800-113032600	Enhancers	HepG2	liver
4	chr1:113032400-113033000	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr1:113033000-113044000	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr1:113034800-113035200	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr1:113036000-113036200	Enhancers	K562	blood
8	chr1:113036200-113036600	Active TSS	K562	blood
9	chr1:113038800-113039200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr1:113039200-113044200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr1:113040000-113044400	Weak transcription	Aorta	Aorta
12	chr1:113040600-113040800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr1:113041600-113041800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr1:113041800-113044400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr1:113042400-113044200	Weak transcription	Right Atrium	heart
16	chr1:113043000-113044000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr1:113043600-113044200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:113043800-113044000	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr1:113043800-113044400	Bivalent Enhancer	Fetal Intestine Large	intestine
20	chr1:113043800-113045400	Bivalent/Poised TSS	Primary T cells from cord blood	blood
21	chr1:113044000-113044200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr1:113044000-113044200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr1:113044000-113044200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr1:113044000-113044200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr1:113044000-113044200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr1:113044000-113044200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr1:113044000-113044200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr1:113044000-113044200	Enhancers	Adipose Nuclei	Adipose
29	chr1:113044000-113044200	Enhancers	Brain Angular Gyrus	brain
30	chr1:113044000-113044200	Enhancers	Brain Hippocampus Middle	brain
31	chr1:113044000-113044200	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr1:113044000-113044200	Enhancers	Brain Substantia Nigra	brain
33	chr1:113044000-113044200	Bivalent Enhancer	Fetal Heart	heart
34	chr1:113044000-113044200	Enhancers	HMEC	breast
35	chr1:113044000-113044200	Enhancers	HUVEC	blood vessel
36	chr1:113044000-113044200	Enhancers	Osteobl	bone
37	chr1:113044000-113044400	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr1:113044000-113044400	Bivalent Enhancer	Liver	Liver
39	chr1:113044000-113044400	Bivalent Enhancer	Fetal Intestine Small	intestine
40	chr1:113044000-113044400	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr1:113044000-113044400	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr1:113044000-113044400	Enhancers	A549	lung
43	chr1:113044000-113044400	Bivalent Enhancer	HepG2	liver
44	chr1:113044000-113044800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
45	chr1:113044200-113044400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
46	chr1:113044200-113044400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
47	chr1:113044200-113044400	Bivalent Enhancer	Primary B cells from cord blood	blood
48	chr1:113044200-113044400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
49	chr1:113044200-113044400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
50	chr1:113044200-113044400	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood

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