Variant report

Variant	esv3343288
Chromosome Location	chr7:87547350-87571066
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:821)
CpG islands
(count:1038)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:821 , 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	chr7:87563499-87563724	HepG2	liver:	n/a	n/a
2	ATF1	chr7:87563123-87563460	K562	blood:	n/a	n/a
3	ATF2	chr7:87562975-87563374	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:87563295-87563839	GM12878	blood:	n/a	n/a
5	ATF2	chr7:87555714-87556481	GM12878	blood:	n/a	n/a
6	ATF2	chr7:87555564-87556499	GM12878	blood:	n/a	n/a
7	BACH1	chr7:87564324-87564681	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:87563085-87563801	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:87555942-87556444	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr7:87555791-87556562	GM12878	blood:	n/a	chr7:87556130-87556141
11	BATF	chr7:87555872-87556285	GM12878	blood:	n/a	chr7:87556130-87556141
12	BCL11A	chr7:87555726-87556343	GM12878	blood:	n/a	n/a
13	BCL11A	chr7:87555821-87556311	GM12878	blood:	n/a	n/a
14	BCL3	chr7:87555880-87556282	GM12878	blood:	n/a	n/a
15	BCL3	chr7:87555874-87556505	GM12878	blood:	n/a	n/a
16	BCLAF1	chr7:87563205-87563918	GM12878	blood:	n/a	chr7:87563654-87563667
17	BCLAF1	chr7:87555770-87556578	GM12878	blood:	n/a	n/a
18	BCLAF1	chr7:87555775-87556448	GM12878	blood:	n/a	n/a
19	BCLAF1	chr7:87563158-87563821	GM12878	blood:	n/a	chr7:87563654-87563667
20	BHLHE40	chr7:87563217-87563614	HepG2	liver:	n/a	n/a
21	BHLHE40	chr7:87555411-87555549	GM12878	blood:	n/a	n/a
22	BHLHE40	chr7:87555854-87556511	GM12878	blood:	n/a	n/a
23	BHLHE40	chr7:87563165-87564881	GM12878	blood:	n/a	n/a
24	BRCA1	chr7:87564872-87564883	GM12878	blood:	n/a	n/a
25	BRCA1	chr7:87563147-87563306	GM12878	blood:	n/a	n/a
26	CCNT2	chr7:87563334-87563897	K562	blood:	n/a	n/a
27	CEBPB	chr7:87555937-87556258	GM12878	blood:	n/a	n/a
28	CEBPB	chr7:87548224-87548416	K562	blood:	n/a	n/a
29	CEBPB	chr7:87555679-87556544	GM12878	blood:	n/a	n/a
30	CEBPB	chr7:87563382-87563659	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr7:87563422-87563603	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr7:87555167-87555264	HepG2	liver:	n/a	n/a
33	CEBPD	chr7:87563337-87563797	HepG2	liver:	n/a	n/a
34	CHD1	chr7:87564628-87564982	GM12878	blood:	n/a	n/a
35	CHD1	chr7:87554968-87555168	GM12878	blood:	n/a	n/a
36	CHD1	chr7:87563529-87564324	H1-hESC	embryonic stem cell:	n/a	chr7:87563754-87563764 chr7:87563697-87563707
37	CHD1	chr7:87555422-87555621	GM12878	blood:	n/a	n/a
38	CHD1	chr7:87563119-87564372	GM12878	blood:	n/a	chr7:87563754-87563764 chr7:87563697-87563707
39	CHD1	chr7:87555942-87556460	GM12878	blood:	n/a	n/a
40	CHD2	chr7:87563276-87563734	Hela-S3	cervix:	n/a	chr7:87563697-87563707
41	CHD2	chr7:87563134-87563799	H1-hESC	embryonic stem cell:	n/a	chr7:87563754-87563764 chr7:87563697-87563707
42	CHD2	chr7:87556144-87556505	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr7:87562901-87564850	GM12878	blood:	n/a	chr7:87563754-87563764 chr7:87563697-87563707
44	CHD2	chr7:87555827-87556493	GM12878	blood:	n/a	n/a
45	CHD2	chr7:87563437-87563731	HepG2	liver:	n/a	chr7:87563697-87563707
46	CHD2	chr7:87555312-87555455	GM12878	blood:	n/a	n/a
47	CREB1	chr7:87563149-87563948	HepG2	liver:	n/a	n/a
48	CREB1	chr7:87563155-87563840	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr7:87563122-87563820	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr7:87563244-87563702	A549	lung:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:87564345-87564395	Caco-2	colon:	n/a
2	chr7:87564345-87564395	Caco-2	colon:	n/a
3	chr7:87563850-87563900	GM06990	blood:	n/a
4	chr7:87568067-87568117	AoSMC	blood vessel:	n/a
5	chr7:87563573-87563623	MCF10A-Er-Src	breast:	n/a
6	chr7:87563649-87563699	SAEC	small airway:	n/a
7	chr7:87563251-87563301	HMEC	breast:	n/a
8	chr7:87563525-87563575	HIPEpiC	eye:	n/a
9	chr7:87563462-87563512	HCM	heart:	n/a
10	chr7:87563850-87563900	AG10803	skin:	n/a
11	chr7:87563908-87563958	RPTEC	kidney:	n/a
12	chr7:87564570-87564620	AoSMC	blood vessel:	n/a
13	chr7:87563569-87563619	MCF10A-Er-Src	breast:	n/a
14	chr7:87563462-87563512	AG04449	skin:	fetal
15	chr7:87568067-87568117	NHBE	bronchial:	n/a
16	chr7:87563717-87563767	SKMC	muscle:	n/a
17	chr7:87564570-87564620	Caco-2	colon:	n/a
18	chr7:87563908-87563958	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:87563495-87563545	LNCaP	prostate:	n/a
20	chr7:87563931-87563981	PFSK-1	brain:	n/a
21	chr7:87563462-87563512	HUVEC	blood vessel:	n/a
22	chr7:87563569-87563619	MCF-7	breast:	n/a
23	chr7:87563573-87563623	HCPEpiC	choroid plexus:	n/a
24	chr7:87564570-87564620	GM12892	blood:	n/a
25	chr7:87563525-87563575	HCT-116	colon:	n/a
26	chr7:87563495-87563545	Hela-S3	cervix:	n/a
27	chr7:87563931-87563981	SKMC	muscle:	n/a
28	chr7:87563495-87563545	Jurkat	blood:	n/a
29	chr7:87564812-87564862	T-47D	breast:	n/a
30	chr7:87563462-87563512	HRCEpiC	kidney:	n/a
31	chr7:87563462-87563512	HNPCEpiC	eye:	n/a
32	chr7:87563850-87563900	AG04450	lung:	fetal
33	chr7:87568067-87568117	HCPEpiC	choroid plexus:	n/a
34	chr7:87563908-87563958	Caco-2	colon:	n/a
35	chr7:87563850-87563900	T-47D	breast:	n/a
36	chr7:87563649-87563699	PrEC	prostate:	n/a
37	chr7:87563850-87563900	Jurkat	blood:	n/a
38	chr7:87564570-87564620	SK-N-SH	brain:	n/a
39	chr7:87563462-87563512	HAEpiC	amniotic membrane:	n/a
40	chr7:87563462-87563512	MCF-7	breast:	n/a
41	chr7:87564812-87564862	H1-hESC	embryonic stem cell:	embryo
42	chr7:87556005-87556055	AoSMC	blood vessel:	n/a
43	chr7:87563649-87563699	HCF	heart:	n/a
44	chr7:87556005-87556055	HEK293	kidney:	embryo
45	chr7:87563850-87563900	HNPCEpiC	eye:	n/a
46	chr7:87563931-87563981	K562	blood:	n/a
47	chr7:87563569-87563619	RPTEC	kidney:	n/a
48	chr7:87563717-87563767	GM12892	blood:	n/a
49	chr7:87564345-87564395	ProgFib	skin:	n/a
50	chr7:87563251-87563301	H1-hESC	embryonic stem cell:	embryo

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:87565506..87567095-chr7:87848014..87850961,2	K562	blood:
2	chr7:87562597..87564742-chr7:87568928..87571613,2	MCF-7	breast:
3	chr7:87563540..87565297-chr7:87569900..87572120,2	MCF-7	breast:
4	chr7:87566977..87569850-chr7:87573658..87575499,2	K562	blood:
5	chr7:87562670..87564637-chr7:87565958..87568571,2	MCF-7	breast:
6	chr7:87554924..87556875-chr7:87615962..87617797,2	MCF-7	breast:

No data

Variant related genes	Relation type
ADAM22	TF binding region
ADAM22	CpG island
ENSG00000075142	chromatin interactions
ENSG00000008277	chromatin interactions
ENSG00000228113	chromatin interactions

Extended variants
information (count: 667 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:667 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536642410	chr7:87547410-87547411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs113969859	chr7:87547468-87547469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559689904	chr7:87547575-87547576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555079765	chr7:87547586-87547587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182086948	chr7:87547644-87547645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551127203	chr7:87547753-87547754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534389239	chr7:87547773-87547774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143645976	chr7:87547791-87547792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146256890	chr7:87547794-87547795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545289139	chr7:87547802-87547803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573413773	chr7:87547809-87547810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530670712	chr7:87547818-87547819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs185794750	chr7:87547821-87547822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545703379	chr7:87547858-87547859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576421941	chr7:87547893-87547894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543823326	chr7:87547939-87547940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs73200356	chr7:87547968-87547969	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs529428564	chr7:87547993-87547994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs180969836	chr7:87548007-87548008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370299610	chr7:87548101-87548102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs565595879	chr7:87548158-87548159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530900432	chr7:87548159-87548160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs2023193	chr7:87548161-87548162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs567542006	chr7:87548201-87548202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs79485113	chr7:87548285-87548286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552094386	chr7:87548320-87548321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs148452989	chr7:87548323-87548324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570240451	chr7:87548356-87548357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs142720280	chr7:87548382-87548383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs548594038	chr7:87548384-87548385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561391516	chr7:87548391-87548392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs185582554	chr7:87548455-87548456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190247576	chr7:87548520-87548521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs55752682	chr7:87548546-87548547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs552743736	chr7:87548577-87548578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs151015675	chr7:87548607-87548608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs34177105	chr7:87548622-87548623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571685134	chr7:87548639-87548640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538444330	chr7:87548732-87548733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557256090	chr7:87548818-87548819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs575587656	chr7:87548850-87548851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs181462166	chr7:87548903-87548904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186050909	chr7:87548972-87548973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192000608	chr7:87549063-87549064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs541561772	chr7:87549074-87549075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs140864081	chr7:87549162-87549163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183812359	chr7:87549177-87549178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs557546481	chr7:87549204-87549205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs144210057	chr7:87549294-87549295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563879999	chr7:87549295-87549296	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	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
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	16616336	CNVD
Burkitt''s lymphoma	19759907	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:561 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:87529400-87547800	Weak transcription	NHEK	skin
2	chr7:87535800-87547800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr7:87537200-87547800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr7:87547800-87548200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:87547800-87548600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr7:87547800-87549400	Enhancers	NHEK	skin
7	chr7:87548400-87549400	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr7:87551400-87551800	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr7:87551600-87552200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr7:87551600-87552200	Flanking Active TSS	GM12878-XiMat	blood
11	chr7:87551600-87555400	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr7:87551800-87555400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr7:87551800-87555800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:87552200-87552400	Active TSS	GM12878-XiMat	blood
15	chr7:87552200-87555800	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr7:87552400-87552600	Flanking Active TSS	GM12878-XiMat	blood
17	chr7:87552600-87553400	Active TSS	GM12878-XiMat	blood
18	chr7:87553400-87554000	Enhancers	GM12878-XiMat	blood
19	chr7:87554000-87554200	Weak transcription	GM12878-XiMat	blood
20	chr7:87554200-87556000	Active TSS	GM12878-XiMat	blood
21	chr7:87554400-87556200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr7:87555000-87555400	Enhancers	Fetal Intestine Large	intestine
23	chr7:87555200-87556400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr7:87555200-87557000	Enhancers	Fetal Intestine Small	intestine
25	chr7:87555400-87555600	Flanking Active TSS	Fetal Intestine Large	intestine
26	chr7:87555400-87556000	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr7:87555400-87556400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr7:87555400-87557000	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr7:87555600-87555800	Enhancers	Fetal Intestine Large	intestine
30	chr7:87555800-87556000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr7:87555800-87556000	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr7:87555800-87556000	Flanking Active TSS	Fetal Intestine Large	intestine
33	chr7:87555800-87556200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr7:87555800-87556400	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr7:87555800-87556600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr7:87555800-87556800	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr7:87555800-87556800	Enhancers	H1 Cell Line	embryonic stem cell
38	chr7:87555800-87556800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr7:87555800-87556800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr7:87555800-87556800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr7:87555800-87556800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr7:87555800-87557000	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr7:87556000-87556400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
44	chr7:87556000-87556400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr7:87556000-87556400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr7:87556000-87556400	Enhancers	Sigmoid Colon	Sigmoid Colon
47	chr7:87556000-87556400	Enhancers	A549	lung
48	chr7:87556000-87556400	Flanking Bivalent TSS/Enh	HepG2	liver
49	chr7:87556000-87556600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr7:87556000-87556600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell

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