Variant report

Variant	nsv888557
Chromosome Location	chr7:80813081-80917148
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:842)
CpG islands
(count:0)
Chromatin interactive
region (count:76)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:842 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:80838216-80838678	K562	blood:	n/a	n/a
2	ARID3A	chr7:80874461-80874519	K562	blood:	n/a	n/a
3	ARID3A	chr7:80886356-80886529	K562	blood:	n/a	n/a
4	ARID3A	chr7:80835779-80836220	K562	blood:	n/a	n/a
5	ARID3A	chr7:80846463-80846580	K562	blood:	n/a	n/a
6	ATF1	chr7:80838347-80838672	K562	blood:	n/a	n/a
7	ATF2	chr7:80874627-80875086	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr7:80838360-80838725	K562	blood:	n/a	n/a
9	BACH1	chr7:80886355-80886632	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:80893499-80893817	K562	blood:	n/a	n/a
11	BACH1	chr7:80893571-80893822	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr7:80874764-80874978	H1-hESC	embryonic stem cell:	n/a	n/a
13	BHLHE40	chr7:80814503-80814642	GM12878	blood:	n/a	n/a
14	BHLHE40	chr7:80838287-80838633	K562	blood:	n/a	n/a
15	CBX3	chr7:80889474-80889879	HCT-116	colon:	n/a	n/a
16	CBX3	chr7:80896810-80897106	K562	blood:	n/a	n/a
17	CBX3	chr7:80838275-80838711	K562	blood:	n/a	n/a
18	CBX3	chr7:80913796-80914251	HCT-116	colon:	n/a	n/a
19	CBX3	chr7:80873489-80873978	HCT-116	colon:	n/a	n/a
20	CBX3	chr7:80889413-80889815	K562	blood:	n/a	n/a
21	CBX3	chr7:80889513-80889730	K562	blood:	n/a	n/a
22	CBX3	chr7:80822827-80823135	K562	blood:	n/a	n/a
23	CCNT2	chr7:80818957-80819157	K562	blood:	n/a	n/a
24	CCNT2	chr7:80838362-80838771	K562	blood:	n/a	n/a
25	CCNT2	chr7:80834045-80834218	K562	blood:	n/a	n/a
26	CEBPB	chr7:80896934-80897025	HepG2	liver:	n/a	chr7:80897004-80897015
27	CEBPB	chr7:80827252-80827531	K562	blood:	n/a	n/a
28	CEBPB	chr7:80893383-80893846	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr7:80873507-80873917	MCF-7	breast:	n/a	n/a
30	CEBPB	chr7:80893405-80893758	ECC-1	luminal epithelium:	n/a	n/a
31	CEBPB	chr7:80900164-80900321	K562	blood:	n/a	chr7:80900245-80900258 chr7:80900247-80900258
32	CEBPB	chr7:80873305-80873803	IMR90	lung:	n/a	chr7:80873392-80873403
33	CEBPB	chr7:80873309-80873732	HepG2	liver:	n/a	chr7:80873392-80873403
34	CEBPB	chr7:80852613-80852815	MCF-7	breast:	n/a	n/a
35	CEBPB	chr7:80864205-80864452	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr7:80835854-80836018	HepG2	liver:	n/a	chr7:80835919-80835930
37	CEBPB	chr7:80896806-80897201	ECC-1	luminal epithelium:	n/a	chr7:80897004-80897015
38	CEBPB	chr7:80820440-80820530	HepG2	liver:	n/a	n/a
39	CEBPB	chr7:80816248-80816426	IMR90	lung:	n/a	chr7:80816258-80816269 chr7:80816401-80816414
40	CEBPB	chr7:80864211-80864470	IMR90	lung:	n/a	n/a
41	CEBPB	chr7:80820218-80820794	HCT-116	colon:	n/a	n/a
42	CEBPB	chr7:80898031-80898148	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr7:80898012-80898417	IMR90	lung:	n/a	n/a
44	CEBPB	chr7:80838239-80838775	K562	blood:	n/a	n/a
45	CEBPB	chr7:80864257-80864402	A549	lung:	n/a	n/a
46	CEBPB	chr7:80820356-80820699	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr7:80839883-80840375	A549	lung:	n/a	n/a
48	CEBPB	chr7:80827352-80827377	IMR90	lung:	n/a	n/a
49	CEBPB	chr7:80839458-80840295	IMR90	lung:	n/a	n/a
50	CEBPB	chr7:80838366-80838630	K562	blood:	n/a	n/a

No data

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:80878793..80880678-chr7:80882418..80884824,2	MCF-7	breast:
2	chr7:80819982..80822822-chr7:80829998..80832398,2	MCF-7	breast:
3	chr7:80886551..80889533-chr7:80889914..80891522,2	MCF-7	breast:
4	chr7:80814937..80817852-chr7:80819181..80821334,2	K562	blood:
5	chr7:80873599..80875269-chr7:80889100..80891084,2	K562	blood:
6	chr7:80860012..80862237-chr7:80868922..80870450,2	MCF-7	breast:
7	chr7:80549184..80550786-chr7:80865135..80867870,2	MCF-7	breast:
8	chr7:80874756..80878864-chr7:80882916..80885687,3	MCF-7	breast:
9	chr7:80852495..80856208-chr7:80856677..80858955,3	K562	blood:
10	chr7:80831342..80833454-chr7:80845026..80847942,2	MCF-7	breast:
11	chr7:80887573..80889363-chr7:80895949..80898235,2	MCF-7	breast:
12	chr7:80884647..80887229-chr7:80899126..80901449,2	MCF-7	breast:
13	chr7:80821320..80824042-chr7:80830231..80831994,2	MCF-7	breast:
14	chr7:80858692..80860259-chr7:80861718..80863525,2	MCF-7	breast:
15	chr7:80814937..80817852-chr7:80819181..80821334,2	K562	blood:
16	chr7:80883750..80886703-chr7:80894705..80896223,2	MCF-7	breast:
17	chr7:80858692..80860259-chr7:80861718..80863525,2	MCF-7	breast:
18	chr7:80878967..80881454-chr7:80884468..80886098,2	MCF-7	breast:
19	chr7:80886551..80889533-chr7:80889914..80891522,2	MCF-7	breast:
20	chr7:80811160..80813261-chr7:80817973..80820541,2	K562	blood:
21	chr7:80548614..80550203-chr7:80841572..80844375,2	MCF-7	breast:
22	chr7:80550385..80552330-chr7:80878720..80881431,3	MCF-7	breast:
23	chr7:80880483..80882765-chr7:80886437..80888337,2	MCF-7	breast:
24	chr7:80828235..80830977-chr7:80837024..80839340,2	K562	blood:
25	chr7:80884647..80887229-chr7:80899126..80901449,2	MCF-7	breast:
26	chr7:80546214..80546714-chr7:80886119..80886785,2	MCF-7	breast:
27	chr7:80873781..80875540-chr7:80877890..80879810,2	MCF-7	breast:
28	chr7:80831342..80833454-chr7:80845026..80847942,2	MCF-7	breast:
29	chr7:80548873..80550374-chr7:80829934..80832081,2	MCF-7	breast:
30	chr7:80884770..80887178-chr7:81075259..81077204,2	MCF-7	breast:
31	chr7:80570359..80572811-chr7:80898526..80900514,2	MCF-7	breast:
32	chr7:80874756..80878864-chr7:80882916..80885687,3	MCF-7	breast:
33	chr7:80544766..80552951-chr7:80883361..80891908,25	MCF-7	breast:
34	chr7:80706504..80708555-chr7:80881256..80882974,2	MCF-7	breast:
35	chr7:80545834..80553200-chr7:80879354..80888784,34	MCF-7	breast:
36	chr7:80548259..80551007-chr7:80894287..80896652,3	MCF-7	breast:
37	chr7:80814459..80816585-chr7:80820535..80822781,3	K562	blood:
38	chr7:80538890..80541410-chr7:80883326..80886321,2	MCF-7	breast:
39	chr7:80545653..80550046-chr7:80890283..80894244,7	MCF-7	breast:
40	chr7:80547067..80548800-chr7:80871379..80875196,3	MCF-7	breast:
41	chr7:80878793..80880678-chr7:80882418..80884824,2	MCF-7	breast:
42	chr7:80821320..80824042-chr7:80830231..80831994,2	MCF-7	breast:
43	chr7:80543126..80544748-chr7:80884976..80886510,2	MCF-7	breast:
44	chr7:80873781..80875540-chr7:80877890..80879810,2	MCF-7	breast:
45	chr7:80548435..80550350-chr7:80813440..80816113,2	MCF-7	breast:
46	chr7:80873599..80875269-chr7:80889100..80891084,2	K562	blood:
47	chr7:80543196..80546765-chr7:80879476..80881407,3	MCF-7	breast:
48	chr7:80547630..80549968-chr7:80897274..80899600,4	MCF-7	breast:
49	chr7:80880483..80882765-chr7:80886437..80888337,2	MCF-7	breast:
50	chr7:80549150..80551514-chr7:80899704..80901338,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD36-4	chr7:80820714-80821325	NONHSAT121757

No data

Variant related genes	Relation type
ENSG00000237896	TF binding region
ENSG00000226671	TF binding region
ENSG00000226671	chromatin interactions
ENSG00000237896	chromatin interactions
ENSG00000075223	chromatin interactions

Extended variants
information (count: 3882 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:3882 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11978732	chr7:80813081-80813082	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566793702	chr7:80813177-80813178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535712159	chr7:80813182-80813183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548631840	chr7:80813228-80813229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs145644506	chr7:80813265-80813266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537584518	chr7:80813272-80813273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs180918775	chr7:80813278-80813279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs117853793	chr7:80813297-80813298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs73374784	chr7:80813376-80813377	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs183731218	chr7:80813397-80813398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs188099524	chr7:80813402-80813403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542092438	chr7:80813415-80813416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533032774	chr7:80813429-80813430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs980966	chr7:80813445-80813446	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs574882541	chr7:80813476-80813477	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs114808235	chr7:80813495-80813496	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs148893438	chr7:80813500-80813501	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs375189495	chr7:80813547-80813548	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs532858547	chr7:80813587-80813588	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs181582149	chr7:80813593-80813594	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs186344732	chr7:80813608-80813609	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs560374059	chr7:80813615-80813616	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs529251703	chr7:80813657-80813658	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs147005464	chr7:80813676-80813677	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs569133397	chr7:80813717-80813718	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs77321903	chr7:80813723-80813724	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs147627840	chr7:80813739-80813740	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs142162018	chr7:80813795-80813796	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs553176291	chr7:80813796-80813797	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs549114179	chr7:80813804-80813805	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs535784783	chr7:80813833-80813834	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs191887544	chr7:80813840-80813841	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs181501781	chr7:80813843-80813844	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs544216095	chr7:80813878-80813879	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs552744001	chr7:80813895-80813896	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs147065340	chr7:80813903-80813904	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs187470685	chr7:80813920-80813921	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs116525138	chr7:80813980-80813981	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs117514416	chr7:80813981-80813982	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs529111382	chr7:80813985-80813986	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs190924571	chr7:80814002-80814003	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs562794834	chr7:80814017-80814018	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs531474507	chr7:80814082-80814083	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs144672156	chr7:80814108-80814109	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs376872218	chr7:80814110-80814111	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs368453123	chr7:80814172-80814173	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs537383821	chr7:80814336-80814337	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs183314236	chr7:80814342-80814343	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs186944283	chr7:80814384-80814385	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs533511741	chr7:80814440-80814441	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:326 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80803800-80819800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:80805000-80819800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr7:80811800-80814000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:80812800-80816600	Weak transcription	Right Ventricle	heart
5	chr7:80815200-80815400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr7:80815400-80815600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr7:80815400-80816200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr7:80815400-80817400	Enhancers	NHDF-Ad	bronchial
9	chr7:80815600-80816200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr7:80815800-80816200	Enhancers	Muscle Satellite Cultured Cells	--
11	chr7:80815800-80817200	Enhancers	Osteobl	bone
12	chr7:80816000-80816200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr7:80816200-80816800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr7:80816200-80817600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:80816200-80818000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:80816200-80820000	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr7:80816400-80817400	Enhancers	NHLF	lung
18	chr7:80816600-80816800	Enhancers	Psoas Muscle	Psoas
19	chr7:80816600-80817000	Enhancers	Right Ventricle	heart
20	chr7:80816600-80817200	Enhancers	Adipose Nuclei	Adipose
21	chr7:80816800-80817000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr7:80816800-80820000	Weak transcription	Psoas Muscle	Psoas
23	chr7:80817000-80820000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr7:80817200-80820000	Weak transcription	Osteobl	bone
25	chr7:80817200-80820200	Weak transcription	Adipose Nuclei	Adipose
26	chr7:80817400-80819800	Weak transcription	NHLF	lung
27	chr7:80817400-80820000	Weak transcription	NHDF-Ad	bronchial
28	chr7:80817600-80819800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr7:80818000-80819800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:80818400-80818600	Enhancers	Pancreas	Pancrea
31	chr7:80818600-80819400	Enhancers	K562	blood
32	chr7:80818600-80820000	Weak transcription	Pancreas	Pancrea
33	chr7:80819400-80820200	Weak transcription	K562	blood
34	chr7:80819600-80820000	Enhancers	A549	lung
35	chr7:80819600-80821000	Enhancers	Fetal Heart	heart
36	chr7:80819800-80820800	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr7:80819800-80820800	Enhancers	HMEC	breast
38	chr7:80819800-80820800	Enhancers	NHLF	lung
39	chr7:80819800-80821000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr7:80819800-80821000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr7:80819800-80821200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr7:80819800-80821400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr7:80820000-80820200	Enhancers	Psoas Muscle	Psoas
44	chr7:80820000-80820600	Enhancers	Pancreas	Pancrea
45	chr7:80820000-80820800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr7:80820000-80820800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr7:80820000-80820800	Enhancers	Fetal Intestine Small	intestine
48	chr7:80820000-80820800	Enhancers	HSMM	muscle
49	chr7:80820000-80821000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr7:80820000-80821000	Enhancers	Skeletal Muscle Female	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links