Variant report

Variant	nsv512056
Chromosome Location	chr8:95724844-95728443
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	BRCA1	chr8:95725722-95725975	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr8:95726180-95726225	A549	lung:	n/a	n/a
3	CEBPB	chr8:95727038-95727058	K562	blood:	n/a	n/a
4	CTCF	chr8:95725380-95725530	GM12870	blood:	n/a	n/a
5	CTCF	chr8:95725740-95725890	NB4	blood:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
6	CTCF	chr8:95725680-95725830	GM12871	blood:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
7	CTCF	chr8:95725680-95725830	SAEC	small airway:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
8	CTCF	chr8:95725740-95725890	GM12865	blood:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
9	CTCF	chr8:95725700-95725850	HepG2	liver:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
10	CTCF	chr8:95725740-95725890	WERI-Rb-1	eye:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
11	CTCF	chr8:95725760-95725910	GM12864	blood:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
12	CTCF	chr8:95725780-95725930	NHEK	skin:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
13	CTCF	chr8:95725727-95725908	GM20000	blood:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
14	CTCF	chr8:95725740-95725890	Hela-S3	cervix:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
15	CTCF	chr8:95725693-95725915	MCF-7	breast:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
16	CTCF	chr8:95725620-95725770	HAc	cerebellar:	n/a	n/a
17	CTCF	chr8:95725720-95725870	NHDF-neo	bronchial:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
18	CTCF	chr8:95725720-95725870	GM12872	blood:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
19	CTCF	chr8:95725720-95725870	HCPEpiC	choroid plexus:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
20	CTCF	chr8:95725720-95725870	HRPEpiC	eye:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
21	CTCF	chr8:95725700-95725850	GM12875	blood:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
22	CTCF	chr8:95725720-95725870	GM12864	blood:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
23	CTCF	chr8:95725720-95725870	BJ	skin:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
24	CTCF	chr8:95726380-95726530	GM12873	blood:	n/a	n/a
25	CTCF	chr8:95725720-95725870	GM06990	blood:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
26	CTCF	chr8:95725700-95725850	GM12866	blood:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
27	CTCF	chr8:95725720-95725870	AG10803	skin:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
28	CTCF	chr8:95725770-95725861	GM12892	blood:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
29	CTCF	chr8:95725720-95725870	HMF	breast:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
30	CTCF	chr8:95725740-95725890	HPF	lung:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
31	CTCF	chr8:95726280-95726430	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr8:95726140-95726290	HRE	kidney:	n/a	n/a
33	CTCF	chr8:95725555-95725987	K562	blood:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
34	CTCF	chr8:95725738-95725884	GM19239	blood:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
35	CTCF	chr8:95725740-95725890	HCT-116	colon:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
36	CTCF	chr8:95725633-95725897	HepG2	liver:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
37	CTCF	chr8:95725720-95725870	NHLF	lung:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
38	CTCF	chr8:95725474-95726196	SK-N-SH	brain:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
39	CTCF	chr8:95725525-95726101	MCF-7	breast:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
40	CTCF	chr8:95725700-95725850	SK-N-SH_RA	brain:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
41	CTCF	chr8:95725720-95725870	HA-sp	spinal cord:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
42	CTCF	chr8:95725680-95725830	GM12867	blood:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
43	CTCF	chr8:95725760-95725910	A549	lung:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
44	CTCF	chr8:95725700-95725850	K562	blood:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
45	CTCF	chr8:95725666-95725933	Hela-S3	cervix:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
46	CTCF	chr8:95725720-95725870	HCM	heart:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
47	CTCF	chr8:95725720-95725870	HRE	kidney:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
48	CTCF	chr8:95725684-95725918	Gliobla	brain:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
49	CTCF	chr8:95725720-95725870	GM12878	blood:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807
50	CTCF	chr8:95725700-95725850	AG09309	skin:	n/a	chr8:95725784-95725805 chr8:95725790-95725806 chr8:95725789-95725807

No.	Distal block	Cell Line	Cell type
1	chr8:95579645..95580492-chr8:95725361..95725931,2	K562	blood:
2	chr8:95720591..95722406-chr8:95725655..95728435,2	MCF-7	breast:
3	chr8:95727241..95729851-chr8:95730354..95733014,2	K562	blood:
4	chr8:95623526..95627073-chr8:95722461..95725966,5	MCF-7	breast:
5	chr8:95651278..95654428-chr8:95723706..95727705,5	MCF-7	breast:
6	chr8:95724740..95726809-chr8:95728368..95731829,3	K562	blood:

Variant related genes	Relation type
ENSG00000253429	TF binding region
DPY19L4	TF binding region
ENSG00000199701	TF binding region
ENSG00000261437	chromatin interactions
ENSG00000199701	chromatin interactions
ENSG00000156162	chromatin interactions
ENSG00000104413	chromatin interactions
ENSG00000253429	chromatin interactions

Extended variants
information (count: 128 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:128 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577518351	chr8:95724874-95724875	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs200855663	chr8:95724876-95724877	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs546468665	chr8:95724877-95724878	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs36148588	chr8:95724878-95724879	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs182998953	chr8:95724880-95724881	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs56050349	chr8:95724897-95724898	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs12114404	chr8:95724898-95724899	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs190288111	chr8:95724900-95724901	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs373111601	chr8:95724913-95724914	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs13248962	chr8:95724918-95724919	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs572131367	chr8:95725025-95725026	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs540739687	chr8:95725059-95725060	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs183045107	chr8:95725074-95725075	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs7828419	chr8:95725080-95725081	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs35693641	chr8:95725083-95725084	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs35508265	chr8:95725085-95725086	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs146259430	chr8:95725090-95725091	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs574615777	chr8:95725119-95725120	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs563289737	chr8:95725129-95725130	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs532263864	chr8:95725200-95725201	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs541728549	chr8:95725206-95725207	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs371474990	chr8:95725208-95725209	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs552383437	chr8:95725214-95725215	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs71273363	chr8:95725226-95725227	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs13260827	chr8:95725259-95725260	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs60642684	chr8:95725313-95725314	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs57262115	chr8:95725314-95725315	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs397942500	chr8:95725333-95725334	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs148088906	chr8:95725353-95725354	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs200364760	chr8:95725370-95725371	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs548359409	chr8:95725376-95725377	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs187738981	chr8:95725379-95725380	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs565072832	chr8:95725470-95725471	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs537397823	chr8:95725481-95725482	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs557392162	chr8:95725507-95725508	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs577654431	chr8:95725535-95725536	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs141834593	chr8:95725553-95725554	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs150652711	chr8:95725597-95725598	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs527459223	chr8:95725604-95725605	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs192411369	chr8:95725635-95725636	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs139750986	chr8:95725641-95725642	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs185602940	chr8:95725656-95725657	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs574190579	chr8:95725701-95725702	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs9918861	chr8:95725733-95725734	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs552084852	chr8:95725757-95725758	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs114245543	chr8:95725782-95725783	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs117102017	chr8:95725789-95725790	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs562929106	chr8:95725796-95725797	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs570489348	chr8:95725805-95725806	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs188037862	chr8:95725817-95725818	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

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
Acute lymphoblastic leukemia	18458336	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
Epilepsy	20502679	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	17847001	CNVD
Neuropsychiatric disorder	20069037	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17142309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95712600-95728800	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr8:95713000-95730600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr8:95714400-95731400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:95716200-95730800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr8:95717200-95730800	Weak transcription	Fetal Intestine Small	intestine
6	chr8:95718400-95731400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr8:95718600-95726200	Weak transcription	NHEK	skin
8	chr8:95718800-95731200	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr8:95719200-95730800	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr8:95719400-95730400	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr8:95719400-95730800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr8:95719400-95731000	Weak transcription	Placenta	Placenta
13	chr8:95719600-95726200	Weak transcription	HMEC	breast
14	chr8:95719600-95731000	Weak transcription	Duodenum Mucosa	Duodenum
15	chr8:95719800-95726400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr8:95719800-95727000	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr8:95719800-95727000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr8:95719800-95730400	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr8:95720000-95731000	Weak transcription	Fetal Intestine Large	intestine
20	chr8:95720200-95731000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr8:95720200-95731000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr8:95720400-95730800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr8:95720600-95726000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr8:95720800-95726200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr8:95723000-95731000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr8:95724600-95731000	Weak transcription	Primary hematopoietic stem cells	blood
27	chr8:95725200-95730800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr8:95726000-95726800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr8:95726200-95726600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr8:95726200-95726600	Enhancers	HMEC	breast
31	chr8:95726200-95726600	Enhancers	NHEK	skin
32	chr8:95726400-95726800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr8:95726600-95730600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr8:95726600-95731000	Weak transcription	HMEC	breast
35	chr8:95726600-95731000	Weak transcription	NHEK	skin
36	chr8:95726800-95730800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr8:95726800-95730800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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