Variant report

Variant	nsv523850
Chromosome Location	chr8:102841031-102893626
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:400)
CpG islands
(count:61)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:400 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:102854400-102854466	K562	blood:	n/a	n/a
2	ATF2	chr8:102858789-102859307	GM12878	blood:	n/a	n/a
3	ATF2	chr8:102854982-102855874	GM12878	blood:	n/a	n/a
4	ATF2	chr8:102855019-102855788	GM12878	blood:	n/a	n/a
5	BACH1	chr8:102876039-102876124	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr8:102858786-102859207	GM12878	blood:	n/a	chr8:102858993-102859004
7	BATF	chr8:102855126-102855769	GM12878	blood:	n/a	chr8:102855445-102855456
8	BATF	chr8:102858820-102859151	GM12878	blood:	n/a	chr8:102858993-102859004
9	BATF	chr8:102855111-102855830	GM12878	blood:	n/a	chr8:102855445-102855456
10	BCL11A	chr8:102855465-102855759	GM12878	blood:	n/a	n/a
11	BCL11A	chr8:102855336-102855836	GM12878	blood:	n/a	n/a
12	BCL3	chr8:102855177-102855774	GM12878	blood:	n/a	n/a
13	BCLAF1	chr8:102855069-102855789	GM12878	blood:	n/a	n/a
14	BCLAF1	chr8:102855021-102855772	GM12878	blood:	n/a	n/a
15	BHLHE40	chr8:102858848-102859248	GM12878	blood:	n/a	n/a
16	BHLHE40	chr8:102853520-102853731	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:102854974-102855834	GM12878	blood:	n/a	n/a
18	CEBPB	chr8:102845487-102845808	HepG2	liver:	n/a	chr8:102845632-102845643
19	CEBPB	chr8:102845499-102845782	K562	blood:	n/a	chr8:102845632-102845643
20	CEBPB	chr8:102845497-102845811	A549	lung:	n/a	chr8:102845632-102845643
21	CEBPB	chr8:102879656-102879695	HepG2	liver:	n/a	n/a
22	CEBPB	chr8:102845492-102845803	IMR90	lung:	n/a	chr8:102845632-102845643
23	CEBPB	chr8:102845243-102845839	MCF-7	breast:	n/a	chr8:102845632-102845643
24	CEBPB	chr8:102844588-102845155	MCF-7	breast:	n/a	n/a
25	CEBPB	chr8:102855249-102855994	GM12878	blood:	n/a	n/a
26	CEBPB	chr8:102867001-102867126	A549	lung:	n/a	n/a
27	CEBPB	chr8:102844759-102845014	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr8:102858761-102859100	GM12878	blood:	n/a	n/a
29	CHD2	chr8:102855062-102855844	GM12878	blood:	n/a	n/a
30	CTCF	chr8:102858960-102859110	MCF-7	breast:	n/a	n/a
31	CTCF	chr8:102864540-102864690	GM12869	blood:	n/a	n/a
32	CTCF	chr8:102859060-102859210	HMF	breast:	n/a	n/a
33	CTCF	chr8:102845080-102845230	MCF-7	breast:	n/a	n/a
34	CTCF	chr8:102858880-102859030	GM12872	blood:	n/a	n/a
35	CTCF	chr8:102859060-102859210	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr8:102859020-102859170	GM12878	blood:	n/a	n/a
37	CTCF	chr8:102859060-102859210	GM12875	blood:	n/a	n/a
38	CTCF	chr8:102845260-102845410	NHEK	skin:	n/a	chr8:102845325-102845346
39	CTCF	chr8:102869093-102869124	ProgFib	skin:	n/a	n/a
40	CTCF	chr8:102859020-102859170	GM12873	blood:	n/a	n/a
41	CTCF	chr8:102859040-102859190	GM12873	blood:	n/a	n/a
42	CTCF	chr8:102859087-102859192	K562	blood:	n/a	n/a
43	CTCF	chr8:102887840-102887990	GM12869	blood:	n/a	n/a
44	CTCF	chr8:102845180-102845330	NHEK	skin:	n/a	n/a
45	CTCF	chr8:102864215-102864280	GM19239	blood:	n/a	n/a
46	CTCF	chr8:102859040-102859190	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr8:102859040-102859190	HMF	breast:	n/a	n/a
48	CTCF	chr8:102859160-102859310	A549	lung:	n/a	n/a
49	CTCF	chr8:102859160-102859310	HVMF	connective:	n/a	n/a
50	CTCF	chr8:102859280-102859430	SAEC	small airway:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:102876411-102876461	HMEC	breast:	n/a
2	chr8:102876411-102876461	GM12891	blood:	n/a
3	chr8:102876411-102876461	HL-60	blood:	n/a
4	chr8:102876411-102876461	HepG2	liver:	n/a
5	chr8:102876411-102876461	Hepatocyte	liver:	n/a
6	chr8:102876411-102876461	NT2-D1	testis:	n/a
7	chr8:102876411-102876461	HCF	heart:	n/a
8	chr8:102876411-102876461	H1-hESC	embryonic stem cell:	embryo
9	chr8:102876411-102876461	GM12878	blood:	n/a
10	chr8:102876411-102876461	U87	brain:	n/a
11	chr8:102876411-102876461	HCM	heart:	n/a
12	chr8:102876411-102876461	HCT-116	colon:	n/a
13	chr8:102876411-102876461	NB4	blood:	n/a
14	chr8:102876411-102876461	AoSMC	blood vessel:	n/a
15	chr8:102876411-102876461	HRCEpiC	kidney:	n/a
16	chr8:102876411-102876461	HIPEpiC	eye:	n/a
17	chr8:102876411-102876461	NH-A	brain:	n/a
18	chr8:102876411-102876461	BE2_C	brain:	n/a
19	chr8:102876411-102876461	HAEpiC	amniotic membrane:	n/a
20	chr8:102876411-102876461	ovcar-3	ovarian:	n/a
21	chr8:102876411-102876461	HUVEC	blood vessel:	n/a
22	chr8:102876411-102876461	SK-N-SH_RA	brain:	n/a
23	chr8:102876411-102876461	PFSK-1	brain:	n/a
24	chr8:102876411-102876461	Hela-S3	cervix:	n/a
25	chr8:102876411-102876461	CMK	blood:	n/a
26	chr8:102876411-102876461	GM19239	blood:	n/a
27	chr8:102876411-102876461	RPTEC	kidney:	n/a
28	chr8:102876411-102876461	SK-N-MC	brain:	n/a
29	chr8:102876411-102876461	AG04450	lung:	fetal
30	chr8:102876411-102876461	NHBE	bronchial:	n/a
31	chr8:102876411-102876461	LNCaP	prostate:	n/a
32	chr8:102876411-102876461	PrEC	prostate:	n/a
33	chr8:102876411-102876461	HNPCEpiC	eye:	n/a
34	chr8:102876411-102876461	SK-N-SH	brain:	n/a
35	chr8:102876411-102876461	ECC-1	luminal epithelium:	n/a
36	chr8:102876411-102876461	HRE	kidney:	n/a
37	chr8:102876411-102876461	HRPEpiC	eye:	n/a
38	chr8:102876411-102876461	BJ	skin:	n/a
39	chr8:102876411-102876461	SAEC	small airway:	n/a
40	chr8:102876411-102876461	HCPEpiC	choroid plexus:	n/a
41	chr8:102876411-102876461	AG09319	gingival:	n/a
42	chr8:102876411-102876461	GM12892	blood:	n/a
43	chr8:102876411-102876461	HPAEpiC	pulmonary alveolar:	n/a
44	chr8:102876411-102876461	GM06990	blood:	n/a
45	chr8:102876411-102876461	HEEpiC	esophagus:	n/a
46	chr8:102876411-102876461	HEK293	kidney:	embryo
47	chr8:102876411-102876461	NHDF-neo	bronchial:	n/a
48	chr8:102876411-102876461	ProgFib	skin:	n/a
49	chr8:102876411-102876461	A549	lung:	n/a
50	chr8:102876411-102876461	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr8:102889173..102891724-chr8:102892647..102895312,2	MCF-7	breast:
2	chr8:102878636..102880767-chr8:102882100..102885005,2	MCF-7	breast:
3	chr8:102889173..102891724-chr8:102892647..102895312,2	MCF-7	breast:
4	chr8:102878654..102880299-chr8:102886876..102888668,2	MCF-7	breast:
5	chr8:102843199..102845818-chr8:102888680..102891293,2	MCF-7	breast:
6	chr8:102847609..102850390-chr8:102853581..102855226,2	MCF-7	breast:
7	chr8:102848832..102850431-chr8:102850962..102852555,2	MCF-7	breast:
8	chr8:102878654..102880299-chr8:102886876..102888668,2	MCF-7	breast:
9	chr8:102847609..102850390-chr8:102853581..102855226,2	MCF-7	breast:
10	chr8:102886318..102888246-chr8:102888335..102890712,2	MCF-7	breast:
11	chr8:102886318..102888246-chr8:102888335..102890712,2	MCF-7	breast:
12	chr8:102857484..102859004-chr8:102860794..102863721,2	K562	blood:
13	chr8:102864772..102866695-chr8:102870312..102872200,2	MCF-7	breast:
14	chr8:97272466..97274308-chr8:102840170..102842402,2	MCF-7	breast:
15	chr8:102841778..102844657-chr8:102844886..102847440,3	K562	blood:
16	chr8:102864772..102866695-chr8:102870312..102872200,2	MCF-7	breast:
17	chr19:27731229..27733214-chr8:102884050..102885632,2	MCF-7	breast:
18	chr8:102841778..102844657-chr8:102844886..102847440,3	K562	blood:
19	chr8:102849681..102851432-chr8:102857073..102859191,2	MCF-7	breast:
20	chr8:102842176..102845083-chr8:102849432..102850991,2	K562	blood:
21	chr8:102857484..102859004-chr8:102860794..102863721,2	K562	blood:
22	chr8:102876704..102878618-chr8:102883254..102885597,2	K562	blood:
23	chr8:102503238..102506028-chr8:102887232..102889960,2	MCF-7	breast:
24	chr17:59368707..59371111-chr8:102843396..102846308,2	MCF-7	breast:
25	chr8:102876704..102878618-chr8:102883254..102885597,2	K562	blood:
26	chr8:102859142..102861704-chr8:102870345..102872066,2	K562	blood:
27	chr8:102848832..102850431-chr8:102850962..102852555,2	MCF-7	breast:
28	chr8:102879891..102881804-chr8:102883261..102884982,2	K562	blood:
29	chr8:102849681..102851432-chr8:102857073..102859191,2	MCF-7	breast:
30	chr8:102842176..102845083-chr8:102849432..102850991,2	K562	blood:
31	chr8:102847583..102849623-chr8:102851249..102854014,2	MCF-7	breast:
32	chr8:102878636..102880767-chr8:102882100..102885005,2	MCF-7	breast:
33	chr8:102843199..102845818-chr8:102888680..102891293,2	MCF-7	breast:
34	chr8:102847583..102849623-chr8:102851249..102854014,2	MCF-7	breast:
35	chr8:102852494..102855006-chr8:102859200..102861225,2	MCF-7	breast:
36	chr8:102879891..102881804-chr8:102883261..102884982,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000238372	TF binding region
ENSG00000238372	CpG island
ENSG00000083307	chromatin interactions
ENSG00000238372	chromatin interactions
ENSG00000156469	chromatin interactions
ENSG00000156471	chromatin interactions
ENSG00000254024	chromatin interactions

Extended variants
information (count: 1946 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:1946 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7827941	chr8:102841031-102841032	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs7827691	chr8:102841065-102841066	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs139269400	chr8:102841107-102841108	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs540239739	chr8:102841169-102841170	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs564829439	chr8:102841180-102841181	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs577228007	chr8:102841189-102841190	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs7828133	chr8:102841194-102841195	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs562781129	chr8:102841223-102841224	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs7828175	chr8:102841361-102841362	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs145432526	chr8:102841383-102841384	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs560280633	chr8:102841391-102841392	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs150811388	chr8:102841397-102841398	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs181049766	chr8:102841406-102841407	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs73696633	chr8:102841449-102841450	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs552161501	chr8:102841458-102841459	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs534527211	chr8:102841461-102841462	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs562403532	chr8:102841507-102841508	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs185311432	chr8:102841524-102841525	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs553156923	chr8:102841581-102841582	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs189715813	chr8:102841622-102841623	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs367832081	chr8:102841629-102841630	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs558177053	chr8:102841638-102841639	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs181231083	chr8:102841682-102841683	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs186204271	chr8:102841706-102841707	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs7828516	chr8:102841716-102841717	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs191958842	chr8:102841724-102841725	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs79844069	chr8:102841802-102841803	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs370924297	chr8:102841857-102841858	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs7840760	chr8:102841881-102841882	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs60177999	chr8:102841887-102841888	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs545877078	chr8:102841888-102841889	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs145616680	chr8:102841898-102841899	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs398068100	chr8:102841903-102841904	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs147697831	chr8:102841954-102841955	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs376621429	chr8:102841956-102841957	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs78143988	chr8:102841957-102841958	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs182715416	chr8:102841984-102841985	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs186290674	chr8:102841995-102841996	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs7841057	chr8:102842005-102842006	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs544186804	chr8:102842086-102842087	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs535707421	chr8:102842091-102842092	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs527795291	chr8:102842106-102842107	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs545862827	chr8:102842123-102842124	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs11775612	chr8:102842157-102842158	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs190849805	chr8:102842159-102842160	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs531627423	chr8:102842168-102842169	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs564258388	chr8:102842183-102842184	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs35295834	chr8:102842202-102842203	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs71268533	chr8:102842203-102842204	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs370057845	chr8:102842236-102842237	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Sezary syndrome	18413736	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Cancer	20164920	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Autism	22495309	CNVD

Chromatin state (count:454 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:102803600-102870600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr8:102832200-102843800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:102834800-102843800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:102835000-102844400	Weak transcription	Psoas Muscle	Psoas
5	chr8:102835000-102852000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr8:102836200-102844400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr8:102836600-102844000	Weak transcription	Fetal Heart	heart
8	chr8:102836600-102844200	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr8:102836800-102843800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr8:102837200-102844000	Weak transcription	Brain Angular Gyrus	brain
11	chr8:102837800-102843800	Weak transcription	Aorta	Aorta
12	chr8:102838600-102848400	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr8:102839600-102843800	Weak transcription	Fetal Muscle Trunk	muscle
14	chr8:102840400-102843400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr8:102840400-102843800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr8:102840400-102843800	Weak transcription	Left Ventricle	heart
17	chr8:102840400-102843800	Weak transcription	NHDF-Ad	bronchial
18	chr8:102840400-102844000	Weak transcription	Stomach Smooth Muscle	stomach
19	chr8:102840400-102844200	Weak transcription	HSMMtube	muscle
20	chr8:102840400-102844400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr8:102840600-102843800	Weak transcription	Rectal Smooth Muscle	rectum
22	chr8:102840600-102844000	Weak transcription	Fetal Muscle Leg	muscle
23	chr8:102840600-102844200	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr8:102840800-102845200	Weak transcription	Adipose Nuclei	Adipose
25	chr8:102841200-102841600	Enhancers	Fetal Kidney	kidney
26	chr8:102841600-102842000	Weak transcription	Fetal Kidney	kidney
27	chr8:102841800-102842400	Enhancers	Fetal Brain Male	brain
28	chr8:102842000-102842200	Enhancers	Fetal Kidney	kidney
29	chr8:102842200-102851000	Weak transcription	Fetal Kidney	kidney
30	chr8:102842400-102844000	Weak transcription	Fetal Brain Male	brain
31	chr8:102843000-102845200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr8:102843000-102845400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr8:102843400-102846200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr8:102843600-102845600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr8:102843800-102844400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr8:102843800-102844400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr8:102843800-102844600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr8:102843800-102844600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr8:102843800-102844600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr8:102843800-102844600	Enhancers	Aorta	Aorta
41	chr8:102843800-102844600	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr8:102843800-102844600	Enhancers	Placenta Amnion	Placenta Amnion
43	chr8:102843800-102844600	Enhancers	Right Ventricle	heart
44	chr8:102843800-102844600	Enhancers	NHDF-Ad	bronchial
45	chr8:102843800-102844600	Enhancers	Osteobl	bone
46	chr8:102843800-102844800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr8:102843800-102844800	Enhancers	Brain Substantia Nigra	brain
48	chr8:102843800-102844800	Enhancers	Ovary	ovary
49	chr8:102843800-102844800	Enhancers	Pancreas	Pancrea
50	chr8:102843800-102844800	Enhancers	Right Atrium	heart

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