Variant report

Variant	nsv979022
Chromosome Location	chr2:73897805-73932073
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	ATF1	chr2:73928292-73928546	K562	blood:	n/a	n/a
4	ATF2	chr2:73901924-73902346	GM12878	blood:	n/a	n/a
5	ATF3	chr2:73903390-73903706	K562	blood:	n/a	n/a
6	BACH1	chr2:73907465-73907526	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr2:73901777-73902343	GM12878	blood:	n/a	n/a
8	BATF	chr2:73911582-73911820	GM12878	blood:	n/a	chr2:73911707-73911718
9	BATF	chr2:73901924-73902350	GM12878	blood:	n/a	n/a
10	BATF	chr2:73917830-73918048	GM12878	blood:	n/a	n/a
11	BCL11A	chr2:73915732-73916019	GM12878	blood:	n/a	n/a
12	BCL11A	chr2:73901938-73902290	GM12878	blood:	n/a	chr2:73902211-73902220 chr2:73902210-73902219
13	BHLHE40	chr2:73917955-73917976	K562	blood:	n/a	n/a
14	BHLHE40	chr2:73928154-73928613	K562	blood:	n/a	n/a
15	CBX3	chr2:73928047-73928946	K562	blood:	n/a	n/a
16	CBX3	chr2:73925299-73925547	K562	blood:	n/a	n/a
17	CBX3	chr2:73925209-73925579	K562	blood:	n/a	n/a
18	CEBPB	chr2:73903410-73903643	K562	blood:	n/a	chr2:73903539-73903550
19	CEBPB	chr2:73900813-73900977	K562	blood:	n/a	chr2:73900873-73900886
20	CEBPB	chr2:73927361-73927552	HepG2	liver:	n/a	chr2:73927522-73927535
21	CEBPB	chr2:73903375-73903643	IMR90	lung:	n/a	chr2:73903539-73903550
22	CEBPB	chr2:73927206-73927852	MCF-7	breast:	n/a	chr2:73927522-73927535
23	CEBPB	chr2:73903365-73903683	K562	blood:	n/a	chr2:73903539-73903550
24	CEBPB	chr2:73927189-73927886	MCF-7	breast:	n/a	chr2:73927522-73927535
25	CEBPB	chr2:73903369-73903615	HepG2	liver:	n/a	chr2:73903539-73903550
26	CEBPB	chr2:73900871-73900878	A549	lung:	n/a	n/a
27	CEBPB	chr2:73903402-73903602	Hela-S3	cervix:	n/a	chr2:73903539-73903550
28	CEBPB	chr2:73926566-73926627	A549	lung:	n/a	n/a
29	CEBPB	chr2:73903437-73903637	H1-hESC	embryonic stem cell:	n/a	chr2:73903539-73903550
30	CEBPB	chr2:73903414-73903663	A549	lung:	n/a	chr2:73903539-73903550
31	CEBPB	chr2:73903357-73903734	K562	blood:	n/a	chr2:73903539-73903550
32	CTCF	chr2:73907420-73907570	K562	blood:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
33	CTCF	chr2:73930971-73931135	K562	blood:	n/a	n/a
34	CTCF	chr2:73907427-73907635	MCF-7	breast:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
35	CTCF	chr2:73918020-73918170	NHDF-neo	bronchial:	n/a	n/a
36	CTCF	chr2:73907440-73907590	HCFaa	heart:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
37	CTCF	chr2:73917867-73918135	GM13976	blood:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012
38	CTCF	chr2:73907800-73907950	AG09319	gingival:	n/a	n/a
39	CTCF	chr2:73907400-73907550	GM12878	blood:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
40	CTCF	chr2:73917920-73918070	GM12873	blood:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012
41	CTCF	chr2:73917940-73918090	GM12872	blood:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012
42	CTCF	chr2:73912140-73912290	AG04449	skin:	n/a	n/a
43	CTCF	chr2:73907305-73907720	A549	lung:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
44	CTCF	chr2:73917897-73918084	H1-hESC	embryonic stem cell:	n/a	chr2:73917996-73918014 chr2:73917998-73918019 chr2:73917997-73918013 chr2:73918001-73918009 chr2:73917999-73918012
45	CTCF	chr2:73912240-73912390	NHLF	lung:	n/a	n/a
46	CTCF	chr2:73917860-73918010	GM12868	blood:	n/a	chr2:73918001-73918009
47	CTCF	chr2:73917328-73917378	GM12892	blood:	n/a	n/a
48	CTCF	chr2:73907348-73907597	GM20000	blood:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
49	CTCF	chr2:73907321-73907685	K562	blood:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
50	CTCF	chr2:73907389-73907637	Hela-S3	cervix:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:73907327-73907377	Jurkat	blood:	n/a
2	chr2:73929892-73929942	SAEC	small airway:	n/a
3	chr2:73929892-73929942	H1-hESC	embryonic stem cell:	embryo
4	chr2:73929892-73929942	Hepatocyte	liver:	n/a
5	chr2:73928500-73928550	A549	lung:	n/a
6	chr2:73907327-73907377	HUVEC	blood vessel:	n/a
7	chr2:73927710-73927760	Jurkat	blood:	n/a
8	chr2:73928348-73928398	LNCaP	prostate:	n/a
9	chr2:73927710-73927760	HepG2	liver:	n/a
10	chr2:73928492-73928542	HL-60	blood:	n/a
11	chr2:73929892-73929942	ECC-1	luminal epithelium:	n/a
12	chr2:73929634-73929684	HMEC	breast:	n/a
13	chr2:73907327-73907377	HL-60	blood:	n/a
14	chr2:73928348-73928398	SKMC	muscle:	n/a
15	chr2:73929634-73929684	HNPCEpiC	eye:	n/a
16	chr2:73927710-73927760	GM06990	blood:	n/a
17	chr2:73929892-73929942	K562	blood:	n/a
18	chr2:73928500-73928550	NB4	blood:	n/a
19	chr2:73907327-73907377	ProgFib	skin:	n/a
20	chr2:73907327-73907377	MCF10A-Er-Src	breast:	n/a
21	chr2:73929765-73929815	RPTEC	kidney:	n/a
22	chr2:73927710-73927760	BJ	skin:	n/a
23	chr2:73929765-73929815	SAEC	small airway:	n/a
24	chr2:73928492-73928542	GM06990	blood:	n/a
25	chr2:73929765-73929815	LNCaP	prostate:	n/a
26	chr2:73929634-73929684	SK-N-MC	brain:	n/a
27	chr2:73928348-73928398	HEEpiC	esophagus:	n/a
28	chr2:73907327-73907377	GM06990	blood:	n/a
29	chr2:73928348-73928398	HRE	kidney:	n/a
30	chr2:73928348-73928398	Jurkat	blood:	n/a
31	chr2:73929765-73929815	NB4	blood:	n/a
32	chr2:73907327-73907377	SK-N-MC	brain:	n/a
33	chr2:73929634-73929684	AG04450	lung:	fetal
34	chr2:73927710-73927760	NHBE	bronchial:	n/a
35	chr2:73929765-73929815	ProgFib	skin:	n/a
36	chr2:73928500-73928550	HL-60	blood:	n/a
37	chr2:73907327-73907377	HCT-116	colon:	n/a
38	chr2:73929634-73929684	NH-A	brain:	n/a
39	chr2:73907327-73907377	HIPEpiC	eye:	n/a
40	chr2:73927710-73927760	AG04450	lung:	fetal
41	chr2:73929765-73929815	HPAEpiC	pulmonary alveolar:	n/a
42	chr2:73928348-73928398	AG09319	gingival:	n/a
43	chr2:73929634-73929684	GM12892	blood:	n/a
44	chr2:73928492-73928542	HEK293	kidney:	embryo
45	chr2:73907327-73907377	HRPEpiC	eye:	n/a
46	chr2:73929765-73929815	T-47D	breast:	n/a
47	chr2:73929765-73929815	ovcar-3	ovarian:	n/a
48	chr2:73928492-73928542	GM12892	blood:	n/a
49	chr2:73928348-73928398	HCF	heart:	n/a
50	chr2:73928500-73928550	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:73846839..73847625-chr2:73907303..73907990,2	MCF-7	breast:
2	chr2:73907073..73907951-chr2:74066396..74067279,2	MCF-7	breast:
3	chr2:73927692..73931050-chr2:73931884..73934947,3	K562	blood:
4	chr2:73906056..73907836-chr2:74356105..74358909,2	MCF-7	breast:
5	chr2:73920861..73923082-chr2:73929614..73932212,2	K562	blood:
6	chr2:73850004..73850829-chr2:73907369..73907993,2	K562	blood:
7	chr2:73920861..73923082-chr2:73929614..73932212,2	K562	blood:
8	chr2:73868945..73872912-chr2:73927731..73932752,4	MCF-7	breast:
9	chr2:73857783..73858474-chr2:73917561..73918197,2	MCF-7	breast:
10	chr2:73931503..73934295-chr2:73936024..73937687,2	MCF-7	breast:
11	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
12	chr2:73846810..73847325-chr2:73907451..73907990,3	K562	blood:
13	chr2:73907051..73907568-chr2:74006793..74007607,2	MCF-7	breast:

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

Variant related genes	Relation type
ALMS1P	TF binding region
ENSG00000204872	TF binding region
ALMS1P	CpG island
ENSG00000204872	CpG island
ENSG00000204872	chromatin interactions
ENSG00000163016	chromatin interactions
ENSG00000144048	chromatin interactions
ENSG00000144035	chromatin interactions
UBE2I	miRNA target sites

Extended variants
information (count: 1665 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1665 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572130509	chr2:73897854-73897855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs149285396	chr2:73897882-73897883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181769761	chr2:73897914-73897915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374760499	chr2:73897937-73897938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529038599	chr2:73897967-73897968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544128096	chr2:73897979-73897980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562075346	chr2:73897981-73897982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs144546616	chr2:73897988-73897989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs148466425	chr2:73898011-73898012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs142330415	chr2:73898017-73898018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566438551	chr2:73898043-73898044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs146824591	chr2:73898061-73898062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs139484603	chr2:73898078-73898079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs567911428	chr2:73898089-73898090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs7570683	chr2:73898118-73898119	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs199539698	chr2:73898128-73898129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571384310	chr2:73898169-73898170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs186124198	chr2:73898219-73898220	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs544453749	chr2:73898229-73898230	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs116768604	chr2:73898246-73898247	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs572068283	chr2:73898280-73898281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs112036611	chr2:73898304-73898305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555634500	chr2:73898343-73898344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs573896183	chr2:73898356-73898357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs4341964	chr2:73898359-73898360	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs190795932	chr2:73898382-73898383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs146623300	chr2:73898396-73898397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545081845	chr2:73898402-73898403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs181711752	chr2:73898408-73898409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186663168	chr2:73898418-73898419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs2421582	chr2:73898420-73898421	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs1344045	chr2:73898461-73898462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370813916	chr2:73898508-73898509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567932101	chr2:73898542-73898543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs113208452	chr2:73898563-73898564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs550082251	chr2:73898573-73898574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs551850793	chr2:73898665-73898666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144078095	chr2:73898681-73898682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571475559	chr2:73898735-73898736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564128206	chr2:73898742-73898743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535230641	chr2:73898765-73898766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs555438336	chr2:73898778-73898779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2421583	chr2:73898785-73898786	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs2421584	chr2:73898852-73898853	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs182904241	chr2:73898853-73898854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs58267559	chr2:73898989-73898990	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs554702371	chr2:73898993-73898994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573860511	chr2:73899210-73899211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537722932	chr2:73899216-73899217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556505843	chr2:73899219-73899220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
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
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:235 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73896200-73905200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr2:73897200-73904600	Weak transcription	Gastric	stomach
3	chr2:73897400-73899600	Weak transcription	Fetal Brain Female	brain
4	chr2:73897600-73899200	Weak transcription	Ovary	ovary
5	chr2:73898000-73898600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr2:73898000-73899600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr2:73898000-73899800	Weak transcription	Brain Angular Gyrus	brain
8	chr2:73898200-73899800	Weak transcription	Liver	Liver
9	chr2:73898200-73899800	Weak transcription	Brain Anterior Caudate	brain
10	chr2:73898400-73900000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr2:73898600-73903600	Weak transcription	Brain Cingulate Gyrus	brain
12	chr2:73898800-73900200	Weak transcription	Pancreas	Pancrea
13	chr2:73898800-73901200	Weak transcription	Brain Substantia Nigra	brain
14	chr2:73899200-73901400	Weak transcription	Brain Hippocampus Middle	brain
15	chr2:73899200-73901600	Strong transcription	Ovary	ovary
16	chr2:73899200-73902200	Weak transcription	Fetal Brain Male	brain
17	chr2:73899400-73902000	Weak transcription	Aorta	Aorta
18	chr2:73899400-73902800	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr2:73899600-73901200	Strong transcription	Fetal Brain Female	brain
20	chr2:73899600-73901400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr2:73899600-73902000	Weak transcription	Fetal Lung	lung
22	chr2:73899800-73900600	Strong transcription	Liver	Liver
23	chr2:73899800-73901400	Strong transcription	Brain Angular Gyrus	brain
24	chr2:73899800-73902200	Strong transcription	Brain Anterior Caudate	brain
25	chr2:73900000-73900600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr2:73900200-73900600	Strong transcription	Pancreas	Pancrea
27	chr2:73900600-73912800	Weak transcription	Liver	Liver
28	chr2:73900600-73913000	Weak transcription	Pancreas	Pancrea
29	chr2:73900600-73954800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr2:73901200-73903400	Weak transcription	Fetal Brain Female	brain
31	chr2:73901400-73905200	Weak transcription	Brain Angular Gyrus	brain
32	chr2:73901400-73913000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr2:73901600-73911400	Weak transcription	Ovary	ovary
34	chr2:73901800-73902400	Enhancers	GM12878-XiMat	blood
35	chr2:73902200-73931400	Weak transcription	Brain Anterior Caudate	brain
36	chr2:73905200-73905600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr2:73906200-73907000	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr2:73906800-73909600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr2:73907000-73907400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
40	chr2:73907000-73907400	Enhancers	H1 Cell Line	embryonic stem cell
41	chr2:73907200-73907400	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr2:73907200-73907400	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr2:73907200-73907400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr2:73911400-73911600	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr2:73911400-73911800	Enhancers	Ovary	ovary
46	chr2:73911800-73912800	Weak transcription	Ovary	ovary
47	chr2:73911800-73913000	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr2:73912600-73913000	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr2:73912800-73913200	Enhancers	HepG2	liver
50	chr2:73912800-73913600	Enhancers	Ovary	ovary

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