Variant report

Variant	nsv874283
Chromosome Location	chr2:73878827-73927764
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	chr2:73907394-73907641	K562	blood:	n/a	n/a
2	ARID3A	chr2:73907372-73907682	HepG2	liver:	n/a	n/a
3	ATF2	chr2:73901924-73902346	GM12878	blood:	n/a	n/a
4	ATF3	chr2:73903390-73903706	K562	blood:	n/a	n/a
5	BACH1	chr2:73907465-73907526	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr2:73911582-73911820	GM12878	blood:	n/a	chr2:73911707-73911718
7	BATF	chr2:73917830-73918048	GM12878	blood:	n/a	n/a
8	BATF	chr2:73901777-73902343	GM12878	blood:	n/a	n/a
9	BATF	chr2:73901924-73902350	GM12878	blood:	n/a	n/a
10	BCL11A	chr2:73915732-73916019	GM12878	blood:	n/a	n/a
11	BCL11A	chr2:73901938-73902290	GM12878	blood:	n/a	chr2:73902211-73902220 chr2:73902210-73902219
12	BHLHE40	chr2:73917955-73917976	K562	blood:	n/a	n/a
13	CBX3	chr2:73925299-73925547	K562	blood:	n/a	n/a
14	CBX3	chr2:73925209-73925579	K562	blood:	n/a	n/a
15	CEBPB	chr2:73903357-73903734	K562	blood:	n/a	chr2:73903539-73903550
16	CEBPB	chr2:73903369-73903615	HepG2	liver:	n/a	chr2:73903539-73903550
17	CEBPB	chr2:73903414-73903663	A549	lung:	n/a	chr2:73903539-73903550
18	CEBPB	chr2:73900871-73900878	A549	lung:	n/a	n/a
19	CEBPB	chr2:73927189-73927886	MCF-7	breast:	n/a	chr2:73927522-73927535
20	CEBPB	chr2:73903410-73903643	K562	blood:	n/a	chr2:73903539-73903550
21	CEBPB	chr2:73927361-73927552	HepG2	liver:	n/a	chr2:73927522-73927535
22	CEBPB	chr2:73903365-73903683	K562	blood:	n/a	chr2:73903539-73903550
23	CEBPB	chr2:73927206-73927852	MCF-7	breast:	n/a	chr2:73927522-73927535
24	CEBPB	chr2:73926566-73926627	A549	lung:	n/a	n/a
25	CEBPB	chr2:73903437-73903637	H1-hESC	embryonic stem cell:	n/a	chr2:73903539-73903550
26	CEBPB	chr2:73900813-73900977	K562	blood:	n/a	chr2:73900873-73900886
27	CEBPB	chr2:73903375-73903643	IMR90	lung:	n/a	chr2:73903539-73903550
28	CEBPB	chr2:73903402-73903602	Hela-S3	cervix:	n/a	chr2:73903539-73903550
29	CTCF	chr2:73907240-73907390	HCM	heart:	n/a	n/a
30	CTCF	chr2:73912240-73912390	HepG2	liver:	n/a	n/a
31	CTCF	chr2:73907440-73907590	GM12864	blood:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
32	CTCF	chr2:73907420-73907570	AG10803	skin:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
33	CTCF	chr2:73917867-73918135	GM13976	blood:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012
34	CTCF	chr2:73907389-73907637	Hela-S3	cervix:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
35	CTCF	chr2:73912240-73912390	GM12874	blood:	n/a	n/a
36	CTCF	chr2:73901987-73902164	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr2:73907420-73907570	K562	blood:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
38	CTCF	chr2:73917660-73917810	HAc	cerebellar:	n/a	n/a
39	CTCF	chr2:73917960-73918110	Hela-S3	cervix:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012
40	CTCF	chr2:73912180-73912330	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr2:73907360-73907610	SK-N-SH_RA	brain:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
42	CTCF	chr2:73879234-73879237	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr2:73917863-73918118	GM12892	blood:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012
44	CTCF	chr2:73917877-73918151	IMR90	lung:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012
45	CTCF	chr2:73912240-73912390	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr2:73912142-73912306	GM13977	blood:	n/a	n/a
47	CTCF	chr2:73917857-73918116	LNCaP	prostate:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012
48	CTCF	chr2:73917940-73918090	HVMF	connective:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012
49	CTCF	chr2:73907420-73907570	HA-sp	spinal cord:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
50	CTCF	chr2:73917882-73918118	GM20000	blood:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:73927710-73927760	AG04449	skin:	fetal
2	chr2:73927710-73927760	AG04449	skin:	fetal
3	chr2:73927710-73927760	Caco-2	colon:	n/a
4	chr2:73927710-73927760	GM06990	blood:	n/a
5	chr2:73907327-73907377	NH-A	brain:	n/a
6	chr2:73927710-73927760	HepG2	liver:	n/a
7	chr2:73907327-73907377	AG04450	lung:	fetal
8	chr2:73907327-73907377	Hepatocyte	liver:	n/a
9	chr2:73927710-73927760	GM12891	blood:	n/a
10	chr2:73927710-73927760	ECC-1	luminal epithelium:	n/a
11	chr2:73927710-73927760	ProgFib	skin:	n/a
12	chr2:73927710-73927760	Jurkat	blood:	n/a
13	chr2:73907327-73907377	LNCaP	prostate:	n/a
14	chr2:73907327-73907377	HNPCEpiC	eye:	n/a
15	chr2:73927710-73927760	AG09319	gingival:	n/a
16	chr2:73927710-73927760	NHDF-neo	bronchial:	n/a
17	chr2:73927710-73927760	HRCEpiC	kidney:	n/a
18	chr2:73907327-73907377	PFSK-1	brain:	n/a
19	chr2:73907327-73907377	IMR90	lung:	fetal
20	chr2:73907327-73907377	SK-N-SH	brain:	n/a
21	chr2:73927710-73927760	HPAEpiC	pulmonary alveolar:	n/a
22	chr2:73907327-73907377	HEEpiC	esophagus:	n/a
23	chr2:73907327-73907377	BE2_C	brain:	n/a
24	chr2:73927710-73927760	SK-N-SH_RA	brain:	n/a
25	chr2:73927710-73927760	U87	brain:	n/a
26	chr2:73927710-73927760	PANC-1	pancreas:	n/a
27	chr2:73927710-73927760	HCF	heart:	n/a
28	chr2:73927710-73927760	NT2-D1	testis:	n/a
29	chr2:73907327-73907377	AoSMC	blood vessel:	n/a
30	chr2:73927710-73927760	HCPEpiC	choroid plexus:	n/a
31	chr2:73927710-73927760	AG09309	skin:	n/a
32	chr2:73907327-73907377	CMK	blood:	n/a
33	chr2:73907327-73907377	Hela-S3	cervix:	n/a
34	chr2:73907327-73907377	HCT-116	colon:	n/a
35	chr2:73907327-73907377	HMEC	breast:	n/a
36	chr2:73927710-73927760	NB4	blood:	n/a
37	chr2:73927710-73927760	SAEC	small airway:	n/a
38	chr2:73907327-73907377	ECC-1	luminal epithelium:	n/a
39	chr2:73927710-73927760	GM19239	blood:	n/a
40	chr2:73907327-73907377	GM12892	blood:	n/a
41	chr2:73907327-73907377	NHDF-neo	bronchial:	n/a
42	chr2:73927710-73927760	HEK293	kidney:	embryo
43	chr2:73927710-73927760	AG10803	skin:	n/a
44	chr2:73927710-73927760	SK-N-MC	brain:	n/a
45	chr2:73927710-73927760	K562	blood:	n/a
46	chr2:73907327-73907377	GM19239	blood:	n/a
47	chr2:73907327-73907377	AG10803	skin:	n/a
48	chr2:73927710-73927760	CMK	blood:	n/a
49	chr2:73927710-73927760	GM12892	blood:	n/a
50	chr2:73907327-73907377	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:73920861..73923082-chr2:73929614..73932212,2	K562	blood:
2	chr2:73880223..73882700-chr2:73884731..73886778,2	K562	blood:
3	chr2:73850004..73850829-chr2:73907369..73907993,2	K562	blood:
4	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
5	chr2:73846839..73847625-chr2:73907303..73907990,2	MCF-7	breast:
6	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
7	chr2:73878117..73880708-chr2:73881565..73884435,2	K562	blood:
8	chr2:73906056..73907836-chr2:74356105..74358909,2	MCF-7	breast:
9	chr2:73857783..73858474-chr2:73917561..73918197,2	MCF-7	breast:
10	chr2:73907051..73907568-chr2:74006793..74007607,2	MCF-7	breast:
11	chr2:73907073..73907951-chr2:74066396..74067279,2	MCF-7	breast:
12	chr2:73868945..73872912-chr2:73927731..73932752,4	MCF-7	breast:
13	chr2:73846810..73847325-chr2:73907451..73907990,3	K562	blood:
14	chr2:73880223..73882700-chr2:73884731..73886778,2	K562	blood:
15	chr2:73878117..73880708-chr2:73881565..73884435,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALMS1-3	chr2:73912088-73912694	NR_003683
2	lnc-ALMS1-3	chr2:73900940-73901123	NR_003683
3	lnc-ALMS1-3	chr2:73898207-73898277	NR_003683
4	lnc-ALMS1-3	chr2:73901969-73902032	NR_003683
5	lnc-ALMS1-3	chr2:73899436-73899622	NR_003683
6	lnc-ALMS1-3	chr2:73899935-73900177	NR_003683
7	lnc-C2orf78-1	chr2:73927556-73928129	ENSG00000251346

Variant related genes	Relation type
ALMS1P	TF binding region
ALMS1P	CpG island
ENSG00000144048	chromatin interactions
ENSG00000144035	chromatin interactions
ENSG00000163016	chromatin interactions
UBE2I	miRNA target sites

Extended variants
information (count: 1604 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1604 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7607989	chr2:73878827-73878828	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs140255110	chr2:73878986-73878987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540544673	chr2:73879049-73879050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556535508	chr2:73879069-73879070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556719136	chr2:73879081-73879082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs536655349	chr2:73879098-73879099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs575122541	chr2:73879132-73879133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs186996468	chr2:73879149-73879150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190785129	chr2:73879160-73879161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs557396424	chr2:73879214-73879215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572859990	chr2:73879220-73879221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs576010296	chr2:73879226-73879227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540178895	chr2:73879273-73879274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs561570569	chr2:73879296-73879297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574261627	chr2:73879320-73879321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544949720	chr2:73879342-73879343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs10175787	chr2:73879361-73879362	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs146523832	chr2:73879367-73879368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs78507650	chr2:73879370-73879371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552015576	chr2:73879438-73879439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs372490299	chr2:73879444-73879445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560589753	chr2:73879488-73879489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs367830068	chr2:73879534-73879535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140811368	chr2:73879538-73879539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs371355387	chr2:73879552-73879553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567584170	chr2:73879575-73879576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs535716435	chr2:73879620-73879621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs541621664	chr2:73879622-73879623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550429920	chr2:73879659-73879660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568825461	chr2:73879699-73879700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558381776	chr2:73879714-73879715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557533027	chr2:73879720-73879721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs183037872	chr2:73879721-73879722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs187287131	chr2:73879795-73879796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs115923767	chr2:73879820-73879821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs573529685	chr2:73879831-73879832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs563390428	chr2:73879886-73879887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191732086	chr2:73879956-73879957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs182919328	chr2:73879974-73879975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs578251638	chr2:73879977-73879978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187512812	chr2:73879980-73879981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545617580	chr2:73879981-73879982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs560560764	chr2:73879994-73879995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs193257404	chr2:73880033-73880034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs150143364	chr2:73880051-73880052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs56193913	chr2:73880074-73880075	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs185404286	chr2:73880194-73880195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs3107529	chr2:73880213-73880214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561453181	chr2:73880414-73880415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189287467	chr2:73880416-73880417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Developmental delay	21147756	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Hepatocellular carcinoma	16750200	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:146 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73876000-73880800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:73878200-73879200	Enhancers	GM12878-XiMat	blood
3	chr2:73878800-73880000	Enhancers	Liver	Liver
4	chr2:73879200-73881600	Weak transcription	GM12878-XiMat	blood
5	chr2:73881600-73882000	Enhancers	GM12878-XiMat	blood
6	chr2:73890800-73891200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:73896200-73905200	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr2:73896800-73897800	Enhancers	HepG2	liver
9	chr2:73897000-73897200	Enhancers	Gastric	stomach
10	chr2:73897200-73904600	Weak transcription	Gastric	stomach
11	chr2:73897400-73899600	Weak transcription	Fetal Brain Female	brain
12	chr2:73897600-73899200	Weak transcription	Ovary	ovary
13	chr2:73898000-73898600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr2:73898000-73899600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr2:73898000-73899800	Weak transcription	Brain Angular Gyrus	brain
16	chr2:73898200-73899800	Weak transcription	Liver	Liver
17	chr2:73898200-73899800	Weak transcription	Brain Anterior Caudate	brain
18	chr2:73898400-73900000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr2:73898600-73903600	Weak transcription	Brain Cingulate Gyrus	brain
20	chr2:73898800-73900200	Weak transcription	Pancreas	Pancrea
21	chr2:73898800-73901200	Weak transcription	Brain Substantia Nigra	brain
22	chr2:73899200-73901400	Weak transcription	Brain Hippocampus Middle	brain
23	chr2:73899200-73901600	Strong transcription	Ovary	ovary
24	chr2:73899200-73902200	Weak transcription	Fetal Brain Male	brain
25	chr2:73899400-73902000	Weak transcription	Aorta	Aorta
26	chr2:73899400-73902800	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr2:73899600-73901200	Strong transcription	Fetal Brain Female	brain
28	chr2:73899600-73901400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
29	chr2:73899600-73902000	Weak transcription	Fetal Lung	lung
30	chr2:73899800-73900600	Strong transcription	Liver	Liver
31	chr2:73899800-73901400	Strong transcription	Brain Angular Gyrus	brain
32	chr2:73899800-73902200	Strong transcription	Brain Anterior Caudate	brain
33	chr2:73900000-73900600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr2:73900200-73900600	Strong transcription	Pancreas	Pancrea
35	chr2:73900600-73912800	Weak transcription	Liver	Liver
36	chr2:73900600-73913000	Weak transcription	Pancreas	Pancrea
37	chr2:73900600-73954800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr2:73901200-73903400	Weak transcription	Fetal Brain Female	brain
39	chr2:73901400-73905200	Weak transcription	Brain Angular Gyrus	brain
40	chr2:73901400-73913000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr2:73901600-73911400	Weak transcription	Ovary	ovary
42	chr2:73901800-73902400	Enhancers	GM12878-XiMat	blood
43	chr2:73902200-73931400	Weak transcription	Brain Anterior Caudate	brain
44	chr2:73905200-73905600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr2:73906200-73907000	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr2:73906800-73909600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr2:73907000-73907400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr2:73907000-73907400	Enhancers	H1 Cell Line	embryonic stem cell
49	chr2:73907200-73907400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr2:73907200-73907400	Enhancers	HUES6 Cell Line	embryonic stem cell

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