Variant report

Variant	nsv437077
Chromosome Location	chr8:104132165-104133226
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:23)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:23 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr8:104132442-104132702	Hela-S3	cervix:	n/a	n/a
2	CTCF	chr8:104132680-104132830	NHEK	skin:	n/a	n/a
3	EP300	chr8:104132543-104132825	SK-N-SH_RA	brain:	n/a	n/a
4	FOS	chr8:104132520-104132766	MCF10A-Er-Src	breast:	n/a	n/a
5	FOS	chr8:104132255-104133085	MCF10A-Er-Src	breast:	n/a	n/a
6	FOS	chr8:104132323-104133085	MCF10A-Er-Src	breast:	n/a	n/a
7	FOS	chr8:104132252-104133174	MCF10A-Er-Src	breast:	n/a	n/a
8	GATA2	chr8:104132516-104132913	SH-SY5Y	brain:	n/a	n/a
9	GATA3	chr8:104132595-104132796	SH-SY5Y	brain:	n/a	n/a
10	GATA3	chr8:104132501-104132867	T-47D	breast:	n/a	n/a
11	GATA3	chr8:104132520-104132894	T-47D	breast:	n/a	n/a
12	GATA3	chr8:104132375-104132863	MCF-7	breast:	n/a	n/a
13	KAP1	chr8:104132452-104133084	U2OS	brain:	n/a	n/a
14	MYC	chr8:104132252-104132880	MCF10A-Er-Src	breast:	n/a	n/a
15	MYC	chr8:104132263-104132870	MCF10A-Er-Src	breast:	n/a	n/a
16	POLR2A	chr8:104132303-104132663	MCF10A-Er-Src	breast:	n/a	n/a
17	POLR2A	chr8:104131940-104132976	MCF10A-Er-Src	breast:	n/a	n/a
18	REST	chr8:104132459-104132886	MCF-7	breast:	n/a	n/a
19	STAT3	chr8:104132322-104132833	MCF10A-Er-Src	breast:	n/a	chr8:104132405-104132417 chr8:104132401-104132413 chr8:104132618-104132626 chr8:104132395-104132407
20	STAT3	chr8:104132291-104132854	MCF10A-Er-Src	breast:	n/a	chr8:104132405-104132417 chr8:104132401-104132413 chr8:104132618-104132626 chr8:104132395-104132407
21	STAT3	chr8:104132514-104132746	MCF10A-Er-Src	breast:	n/a	chr8:104132618-104132626
22	STAT3	chr8:104132424-104133083	MCF10A-Er-Src	breast:	n/a	chr8:104132618-104132626
23	ZNF217	chr8:104132501-104132851	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:104132683-104132733	HPAEpiC	pulmonary alveolar:	n/a
2	chr8:104132683-104132733	HUVEC	blood vessel:	n/a
3	chr8:104132683-104132733	Caco-2	colon:	n/a
4	chr8:104132683-104132733	AG10803	skin:	n/a
5	chr8:104132683-104132733	SK-N-SH_RA	brain:	n/a
6	chr8:104132683-104132733	NHDF-neo	bronchial:	n/a
7	chr8:104132683-104132733	HMEC	breast:	n/a
8	chr8:104132683-104132733	HEK293	kidney:	embryo
9	chr8:104132683-104132733	HCT-116	colon:	n/a
10	chr8:104132683-104132733	SAEC	small airway:	n/a
11	chr8:104132683-104132733	CMK	blood:	n/a
12	chr8:104132683-104132733	AG04450	lung:	fetal
13	chr8:104132683-104132733	HRPEpiC	eye:	n/a
14	chr8:104132683-104132733	NB4	blood:	n/a
15	chr8:104132683-104132733	GM12878	blood:	n/a
16	chr8:104132683-104132733	HRE	kidney:	n/a
17	chr8:104132683-104132733	A549	lung:	n/a
18	chr8:104132683-104132733	HEEpiC	esophagus:	n/a
19	chr8:104132683-104132733	T-47D	breast:	n/a
20	chr8:104132683-104132733	HNPCEpiC	eye:	n/a
21	chr8:104132683-104132733	NH-A	brain:	n/a
22	chr8:104132683-104132733	ProgFib	skin:	n/a
23	chr8:104132683-104132733	K562	blood:	n/a
24	chr8:104132683-104132733	AG04449	skin:	fetal
25	chr8:104132683-104132733	HCF	heart:	n/a
26	chr8:104132683-104132733	AG09309	skin:	n/a
27	chr8:104132683-104132733	GM06990	blood:	n/a
28	chr8:104132683-104132733	PANC-1	pancreas:	n/a
29	chr8:104132683-104132733	BE2_C	brain:	n/a
30	chr8:104132683-104132733	HIPEpiC	eye:	n/a
31	chr8:104132683-104132733	HCPEpiC	choroid plexus:	n/a
32	chr8:104132683-104132733	MCF10A-Er-Src	breast:	n/a
33	chr8:104132683-104132733	HCM	heart:	n/a
34	chr8:104132683-104132733	ECC-1	luminal epithelium:	n/a
35	chr8:104132683-104132733	HRCEpiC	kidney:	n/a
36	chr8:104132683-104132733	PrEC	prostate:	n/a
37	chr8:104132683-104132733	SK-N-SH	brain:	n/a
38	chr8:104132683-104132733	NT2-D1	testis:	n/a
39	chr8:104132683-104132733	Hepatocyte	liver:	n/a
40	chr8:104132683-104132733	HepG2	liver:	n/a
41	chr8:104132683-104132733	Hela-S3	cervix:	n/a
42	chr8:104132683-104132733	SKMC	muscle:	n/a
43	chr8:104132683-104132733	PFSK-1	brain:	n/a
44	chr8:104132683-104132733	RPTEC	kidney:	n/a
45	chr8:104132683-104132733	GM12892	blood:	n/a
46	chr8:104132683-104132733	HL-60	blood:	n/a
47	chr8:104132683-104132733	GM12891	blood:	n/a
48	chr8:104132683-104132733	ovcar-3	ovarian:	n/a
49	chr8:104132683-104132733	AG09319	gingival:	n/a
50	chr8:104132683-104132733	H1-hESC	embryonic stem cell:	embryo

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:104130679..104132364-chr8:104143004..104144519,2	MCF-7	breast:
2	chr8:104131678..104134497-chr8:104225293..104227549,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000250929	TF binding region
ENSG00000250929	CpG island
ENSG00000164929	chromatin interactions

Extended variants
information (count: 42 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:42 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2454037	chr8:104132165-104132166	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536469527	chr8:104132180-104132181	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs186768599	chr8:104132191-104132192	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs549816305	chr8:104132305-104132306	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs533682394	chr8:104132308-104132309	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs76342329	chr8:104132343-104132344	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs71503491	chr8:104132344-104132345	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs2454038	chr8:104132345-104132346	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs111633406	chr8:104132424-104132425	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs556829799	chr8:104132438-104132439	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs62527574	chr8:104132456-104132457	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs144642378	chr8:104132468-104132469	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs560700938	chr8:104132471-104132472	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs117169395	chr8:104132482-104132483	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs543076637	chr8:104132527-104132528	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs546364452	chr8:104132540-104132541	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs564284094	chr8:104132572-104132573	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs561942254	chr8:104132583-104132584	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs191613003	chr8:104132598-104132599	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs76616283	chr8:104132614-104132615	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs184814778	chr8:104132643-104132644	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs151262774	chr8:104132654-104132655	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs566378198	chr8:104132662-104132663	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs533598278	chr8:104132673-104132674	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs368451834	chr8:104132683-104132684	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs188902390	chr8:104132684-104132685	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs4404881	chr8:104132722-104132723	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs116772518	chr8:104132770-104132771	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs3019158	chr8:104132792-104132793	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs371224247	chr8:104132809-104132810	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs2935593	chr8:104132853-104132854	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs575061872	chr8:104132863-104132864	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs139310025	chr8:104132879-104132880	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs554401906	chr8:104132888-104132889	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs193038401	chr8:104132952-104132953	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs114067116	chr8:104133003-104133004	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs200296983	chr8:104133032-104133033	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs546286620	chr8:104133070-104133071	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs149716117	chr8:104133165-104133166	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs111353355	chr8:104133198-104133199	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs145588635	chr8:104133225-104133226	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs3019159	chr8:104133226-104133227	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:114)

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
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
Bladder cancer	21909424	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104119400-104134000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:104122000-104134600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr8:104123600-104132600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:104127400-104133200	Weak transcription	HSMMtube	muscle
5	chr8:104128400-104132800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr8:104128600-104132600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr8:104128600-104133000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr8:104128800-104132400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr8:104128800-104132400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr8:104128800-104132400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr8:104128800-104132600	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr8:104128800-104132600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr8:104128800-104133200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr8:104128800-104134200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr8:104129000-104133400	Weak transcription	Osteobl	bone
16	chr8:104130800-104133000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr8:104131000-104132200	Enhancers	NHEK	skin
18	chr8:104131000-104132800	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr8:104131000-104135200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:104131200-104132200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr8:104131200-104132400	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr8:104131200-104132600	Enhancers	NH-A	brain
23	chr8:104131200-104134000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr8:104131200-104134000	Enhancers	HMEC	breast
25	chr8:104131200-104136400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr8:104131400-104132200	Weak transcription	NHDF-Ad	bronchial
27	chr8:104131600-104132600	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr8:104131600-104133400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr8:104131800-104132200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr8:104131800-104132800	Enhancers	Muscle Satellite Cultured Cells	--
31	chr8:104131800-104133200	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr8:104131800-104133600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr8:104132000-104132400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr8:104132000-104132400	Enhancers	Primary hematopoietic stem cells	blood
35	chr8:104132000-104132400	Enhancers	HSMM	muscle
36	chr8:104132000-104132400	Enhancers	HUVEC	blood vessel
37	chr8:104132000-104132800	Enhancers	Fetal Intestine Large	intestine
38	chr8:104132000-104133000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr8:104132000-104133000	Enhancers	Fetal Intestine Small	intestine
40	chr8:104132000-104133600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr8:104132000-104133800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr8:104132000-104134400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr8:104132200-104132400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr8:104132200-104132400	Flanking Active TSS	Duodenum Mucosa	Duodenum
45	chr8:104132200-104132400	Flanking Active TSS	NHEK	skin
46	chr8:104132200-104132600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr8:104132200-104132600	Enhancers	Fetal Thymus	thymus
48	chr8:104132200-104132600	Enhancers	GM12878-XiMat	blood
49	chr8:104132200-104132800	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr8:104132200-104132800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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