Variant report

Variant	nsv6394
Chromosome Location	chr8:130421502-130446035
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:171)
CpG islands
(count:0)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:171 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:130432838-130433225	K562	blood:	n/a	n/a
2	ATF1	chr8:130426847-130427166	K562	blood:	n/a	n/a
3	ATF1	chr8:130430061-130430286	K562	blood:	n/a	n/a
4	ATF1	chr8:130432735-130433139	K562	blood:	n/a	n/a
5	ATF1	chr8:130437723-130437776	K562	blood:	n/a	n/a
6	ATF2	chr8:130427610-130428253	GM12878	blood:	n/a	n/a
7	BACH1	chr8:130437927-130437931	K562	blood:	n/a	n/a
8	BACH1	chr8:130430708-130431054	K562	blood:	n/a	n/a
9	BCL11A	chr8:130427857-130428072	GM12878	blood:	n/a	n/a
10	BCL3	chr8:130427760-130428195	GM12878	blood:	n/a	n/a
11	BHLHE40	chr8:130427796-130428137	GM12878	blood:	n/a	n/a
12	BHLHE40	chr8:130433027-130433221	K562	blood:	n/a	n/a
13	BRCA1	chr8:130427937-130428111	GM12878	blood:	n/a	n/a
14	CBX3	chr8:130430772-130431220	K562	blood:	n/a	n/a
15	CCNT2	chr8:130426768-130426949	K562	blood:	n/a	n/a
16	CCNT2	chr8:130432890-130433191	K562	blood:	n/a	n/a
17	CEBPB	chr8:130424611-130424813	K562	blood:	n/a	chr8:130424665-130424676 chr8:130424665-130424678
18	CEBPB	chr8:130432684-130432985	K562	blood:	n/a	chr8:130432785-130432798
19	CEBPB	chr8:130424574-130424823	HepG2	liver:	n/a	chr8:130424665-130424676 chr8:130424665-130424678
20	CEBPB	chr8:130424485-130424857	IMR90	lung:	n/a	chr8:130424665-130424676 chr8:130424665-130424678
21	CTCF	chr8:130441191-130441229	LNCaP	prostate:	n/a	n/a
22	CTCF	chr8:130438157-130438212	GM20000	blood:	n/a	n/a
23	CTCF	chr8:130435269-130435356	Fibrobl	skin:	n/a	n/a
24	CUX1	chr8:130432704-130433117	K562	blood:	n/a	n/a
25	E2F4	chr8:130438790-130438966	MCF10A-Er-Src	breast:	n/a	n/a
26	ELF1	chr8:130432729-130433172	K562	blood:	n/a	chr8:130433030-130433041
27	EP300	chr8:130427925-130428150	GM12878	blood:	n/a	n/a
28	EP300	chr8:130427875-130428209	GM12878	blood:	n/a	n/a
29	EP300	chr8:130432701-130433177	K562	blood:	n/a	chr8:130432970-130432984 chr8:130433030-130433039
30	EP300	chr8:130430714-130431135	K562	blood:	n/a	chr8:130430998-130431007
31	FOS	chr8:130431076-130431200	MCF10A-Er-Src	breast:	n/a	chr8:130431126-130431134 chr8:130431127-130431134
32	FOXA1	chr8:130444101-130444454	T-47D	breast:	n/a	n/a
33	FOXA1	chr8:130444212-130444352	ECC-1	luminal epithelium:	n/a	n/a
34	FOXA1	chr8:130423697-130423961	ECC-1	luminal epithelium:	n/a	chr8:130423869-130423881
35	FOXA1	chr8:130444066-130444437	T-47D	breast:	n/a	n/a
36	FOXA1	chr8:130423643-130424079	ECC-1	luminal epithelium:	n/a	chr8:130423869-130423881
37	GATA3	chr8:130428522-130429166	SK-N-SH	brain:	n/a	n/a
38	GATA3	chr8:130443995-130444602	MCF-7	breast:	n/a	n/a
39	GATA3	chr8:130427118-130427256	SH-SY5Y	brain:	n/a	chr8:130427224-130427234
40	GATA3	chr8:130444100-130444501	T-47D	breast:	n/a	n/a
41	HCFC1	chr8:130433186-130433208	K562	blood:	n/a	n/a
42	HDAC2	chr8:130444029-130444571	MCF-7	breast:	n/a	n/a
43	IKZF1	chr8:130427815-130428250	GM12878	blood:	n/a	n/a
44	IRF1	chr8:130432691-130433110	K562	blood:	n/a	n/a
45	IRF1	chr8:130437043-130437061	K562	blood:	n/a	n/a
46	IRF1	chr8:130433552-130433742	K562	blood:	n/a	chr8:130433560-130433574
47	JUN	chr8:130423346-130423351	H1-hESC	embryonic stem cell:	n/a	n/a
48	JUN	chr8:130430738-130431272	K562	blood:	n/a	chr8:130431126-130431134 chr8:130431127-130431134 chr8:130430754-130430762
49	JUND	chr8:130432696-130433223	K562	blood:	n/a	n/a
50	JUND	chr8:130430831-130431261	K562	blood:	n/a	chr8:130431126-130431134 chr8:130431127-130431134

No data

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:130427156..130429100-chr8:130430204..130432175,2	K562	blood:
2	chr8:130443086..130445932-chr8:130472163..130473857,2	MCF-7	breast:
3	chr8:130432582..130435209-chr8:130544896..130547721,2	K562	blood:
4	chr8:130422480..130424858-chr8:130426519..130428589,2	K562	blood:
5	chr8:130424297..130426458-chr8:130429983..130431740,3	K562	blood:
6	chr11:62608631..62609567-chr8:130435702..130436693,2	NB4	blood:
7	chr8:130438496..130440259-chr8:130595633..130598498,2	K562	blood:
8	chr8:130429538..130431900-chr8:130434547..130436688,2	MCF-7	breast:
9	chr8:130433486..130436461-chr8:130437244..130438809,2	K562	blood:
10	chr8:130444302..130447418-chr8:130460105..130463114,3	MCF-7	breast:
11	chr8:130438946..130441544-chr8:130456592..130459697,3	K562	blood:
12	chr8:130429538..130431900-chr8:130434547..130436688,2	MCF-7	breast:
13	chr8:130324110..130326533-chr8:130436449..130439248,2	K562	blood:
14	chr8:130424297..130426458-chr8:130429983..130431740,3	K562	blood:
15	chr8:130419752..130421541-chr8:130425916..130427776,2	K562	blood:
16	chr8:130419285..130421126-chr8:130422291..130424693,2	K562	blood:
17	chr8:130433486..130436461-chr8:130437244..130438809,2	K562	blood:
18	chr8:130419752..130421541-chr8:130425916..130427776,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GSDMC-9	chr8:130433122-130434408	ucscGeneNc_uc003ysq_1

No data

Variant related genes	Relation type
ENSG00000253926	TF binding region
ENSG00000253926	chromatin interactions
ENSG00000133316	chromatin interactions

Extended variants
information (count: 880 )
Associated
traits (count: 153 )

Variant overlapped rSNPs/rCNVs (count:880 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572892897	chr8:130421503-130421504	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540334225	chr8:130421524-130421525	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140059651	chr8:130421527-130421528	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs13259353	chr8:130421568-130421569	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs544487634	chr8:130421584-130421585	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565527194	chr8:130421635-130421636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs57780119	chr8:130421636-130421637	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs539204250	chr8:130421692-130421693	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181841615	chr8:130421719-130421720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560545274	chr8:130421732-130421733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527736032	chr8:130421749-130421750	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552660551	chr8:130421758-130421759	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547796415	chr8:130421784-130421785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs73712635	chr8:130421805-130421806	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs2568413	chr8:130421811-130421812	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs569224753	chr8:130421823-130421824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs376871352	chr8:130421829-130421830	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536244575	chr8:130421838-130421839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs35938360	chr8:130421846-130421847	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs536764702	chr8:130421848-130421849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs111316550	chr8:130421857-130421858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572800463	chr8:130421898-130421899	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2719222	chr8:130421932-130421933	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs144041540	chr8:130421934-130421935	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs577000711	chr8:130421958-130421959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186091059	chr8:130422130-130422131	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560650542	chr8:130422132-130422133	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573707428	chr8:130422158-130422159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190893054	chr8:130422165-130422166	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs985687	chr8:130422184-130422185	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs985688	chr8:130422207-130422208	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs12546163	chr8:130422222-130422223	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs74592066	chr8:130422224-130422225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564601016	chr8:130422267-130422268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532346977	chr8:130422300-130422301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532134497	chr8:130422365-130422366	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148745535	chr8:130422366-130422367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs142247073	chr8:130422367-130422368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536110652	chr8:130422368-130422369	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1813473	chr8:130422403-130422404	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs150829958	chr8:130422414-130422415	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563745385	chr8:130422443-130422444	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114990863	chr8:130422485-130422486	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs368667624	chr8:130422488-130422489	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs576571235	chr8:130422506-130422507	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs115978137	chr8:130422533-130422534	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs556289385	chr8:130422540-130422541	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs574711602	chr8:130422558-130422559	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs139181029	chr8:130422612-130422613	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs554485052	chr8:130422639-130422640	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:153)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Acute myeloid leukemia	20729466	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
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	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
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Malignant melanoma	17260012	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	22048815	CNVD
Colorectal cancer	16912164	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	21148746	CNVD
Lung cancer	21911935	CNVD
Breast cancer	20459607	CNVD
Medulloblastoma	19270706	CNVD
Acute myeloid leukemia	19651601	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	22860045	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Prostate cancer	17217626	CNVD
Cancer	17160897	CNVD
Breast cancer	16497871	CNVD
Colorectal cancer	16882699	CNVD
Cystic fibrosis	19273617	CNVD
Chronic stroke	19622162	CNVD
Chordoma	18071362	CNVD
Breast cancer	17850661	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	16272173	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	20844748	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	16620391	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:173 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130410200-130434600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:130416800-130426600	Strong transcription	K562	blood
3	chr8:130418800-130424000	Weak transcription	Dnd41	blood
4	chr8:130419200-130423400	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr8:130419600-130423600	Weak transcription	Fetal Stomach	stomach
6	chr8:130419800-130423200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr8:130419800-130423600	Weak transcription	Fetal Muscle Leg	muscle
8	chr8:130419800-130425800	Weak transcription	Fetal Thymus	thymus
9	chr8:130419800-130427000	Weak transcription	Thymus	Thymus
10	chr8:130420000-130421600	Enhancers	Fetal Heart	heart
11	chr8:130420000-130424000	Weak transcription	Brain Hippocampus Middle	brain
12	chr8:130421600-130423600	Weak transcription	Fetal Heart	heart
13	chr8:130422400-130422600	Enhancers	Primary B cells from peripheral blood	blood
14	chr8:130422400-130422800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr8:130422400-130423400	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr8:130422600-130423200	Weak transcription	Primary B cells from peripheral blood	blood
17	chr8:130423000-130423800	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr8:130423200-130423800	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr8:130423200-130424000	Enhancers	Primary B cells from peripheral blood	blood
20	chr8:130423400-130423600	Enhancers	Fetal Lung	lung
21	chr8:130423400-130423600	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr8:130423400-130424200	Enhancers	GM12878-XiMat	blood
23	chr8:130423400-130424400	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr8:130423600-130423800	Flanking Active TSS	Fetal Lung	lung
25	chr8:130423600-130424000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
26	chr8:130423600-130424400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr8:130423600-130424400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr8:130423600-130424400	Enhancers	NH-A	brain
29	chr8:130423600-130424600	Enhancers	Fetal Muscle Leg	muscle
30	chr8:130423600-130425000	Enhancers	Fetal Heart	heart
31	chr8:130423600-130425000	Enhancers	Fetal Stomach	stomach
32	chr8:130423800-130424000	Enhancers	Fetal Lung	lung
33	chr8:130423800-130424200	Enhancers	HSMMtube	muscle
34	chr8:130423800-130424400	Enhancers	NHLF	lung
35	chr8:130424000-130424200	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr8:130424000-130424400	Enhancers	Brain Hippocampus Middle	brain
37	chr8:130424000-130424600	Flanking Active TSS	Fetal Lung	lung
38	chr8:130424000-130424600	Enhancers	Psoas Muscle	Psoas
39	chr8:130424000-130425800	Enhancers	Dnd41	blood
40	chr8:130424200-130424600	Enhancers	Brain Cingulate Gyrus	brain
41	chr8:130424200-130424600	Enhancers	Fetal Kidney	kidney
42	chr8:130424200-130426400	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr8:130424200-130427600	Weak transcription	GM12878-XiMat	blood
44	chr8:130424400-130424600	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr8:130424400-130426600	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr8:130424600-130426600	Enhancers	Fetal Lung	lung
47	chr8:130425000-130427800	Weak transcription	Fetal Stomach	stomach
48	chr8:130425800-130426000	Enhancers	Fetal Thymus	thymus
49	chr8:130425800-130426200	Genic enhancers	Dnd41	blood
50	chr8:130426000-130426800	Weak transcription	Fetal Thymus	thymus

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links