Variant report

Variant	esv3479600
Chromosome Location	chr8:90736917-90741003
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:344)
CpG islands
(count:0)
Chromatin interactive
region (count:29)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:344 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:90738052-90738327	K562	blood:	n/a	n/a
2	ARID3A	chr8:90738074-90738343	HepG2	liver:	n/a	n/a
3	ATF1	chr8:90738051-90738334	K562	blood:	n/a	n/a
4	ATF1	chr8:90740926-90741719	K562	blood:	n/a	n/a
5	ATF2	chr8:90737920-90738636	GM12878	blood:	n/a	n/a
6	ATF2	chr8:90737929-90738551	GM12878	blood:	n/a	n/a
7	ATF2	chr8:90738026-90738427	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr8:90738096-90738310	K562	blood:	n/a	n/a
9	BACH1	chr8:90738733-90738759	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr8:90738003-90738500	GM12878	blood:	n/a	chr8:90738291-90738302 chr8:90738292-90738302
11	BATF	chr8:90738011-90738449	GM12878	blood:	n/a	chr8:90738291-90738302 chr8:90738292-90738302
12	BCL3	chr8:90737989-90738504	GM12878	blood:	n/a	chr8:90738122-90738131
13	BCLAF1	chr8:90737957-90738469	GM12878	blood:	n/a	chr8:90738122-90738131
14	BCLAF1	chr8:90737861-90738551	GM12878	blood:	n/a	chr8:90738122-90738131 chr8:90737903-90737912
15	BHLHE40	chr8:90738028-90738733	GM12878	blood:	n/a	n/a
16	BHLHE40	chr8:90738026-90738384	K562	blood:	n/a	n/a
17	BHLHE40	chr8:90740597-90740708	GM12878	blood:	n/a	n/a
18	CBX3	chr8:90737999-90738365	K562	blood:	n/a	n/a
19	CBX3	chr8:90740890-90741741	K562	blood:	n/a	n/a
20	CEBPB	chr8:90740959-90741684	K562	blood:	n/a	chr8:90741231-90741240 chr8:90741231-90741242 chr8:90741229-90741242 chr8:90741229-90741240 chr8:90741229-90741242
21	CEBPB	chr8:90737876-90738616	GM12878	blood:	n/a	n/a
22	CEBPB	chr8:90738187-90738565	IMR90	lung:	n/a	n/a
23	CHD2	chr8:90737963-90738782	GM12878	blood:	n/a	n/a
24	CHD2	chr8:90738073-90738329	K562	blood:	n/a	n/a
25	CREB1	chr8:90738033-90738488	GM12878	blood:	n/a	n/a
26	CREB1	chr8:90737867-90738662	GM12878	blood:	n/a	n/a
27	CTCF	chr8:90738095-90738399	GM10248	blood:	n/a	n/a
28	CTCF	chr8:90738120-90738270	NB4	blood:	n/a	n/a
29	CTCF	chr8:90738180-90738330	GM12872	blood:	n/a	n/a
30	CTCF	chr8:90738140-90738290	GM12867	blood:	n/a	n/a
31	CTCF	chr8:90738120-90738270	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr8:90738072-90738334	Spleen_OC	spleen:	n/a	n/a
33	CTCF	chr8:90738160-90738310	NHDF-neo	bronchial:	n/a	n/a
34	CTCF	chr8:90738120-90738270	HCT-116	colon:	n/a	n/a
35	CTCF	chr8:90738100-90738250	MCF-7	breast:	n/a	n/a
36	CTCF	chr8:90738140-90738290	GM12864	blood:	n/a	n/a
37	CTCF	chr8:90738080-90738230	NHEK	skin:	n/a	n/a
38	CTCF	chr8:90738120-90738270	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr8:90738100-90738250	NHLF	lung:	n/a	n/a
40	CTCF	chr8:90737979-90738401	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr8:90738140-90738290	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr8:90738140-90738290	HEK293	kidney:	n/a	n/a
43	CTCF	chr8:90738120-90738270	HAc	cerebellar:	n/a	n/a
44	CTCF	chr8:90738120-90738270	HMF	breast:	n/a	n/a
45	CTCF	chr8:90738140-90738290	GM12873	blood:	n/a	n/a
46	CTCF	chr8:90738093-90738323	GM10266	blood:	n/a	n/a
47	CTCF	chr8:90738114-90738273	NHEK	skin:	n/a	n/a
48	CTCF	chr8:90738097-90738335	K562	blood:	n/a	n/a
49	CTCF	chr8:90738140-90738290	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr8:90738128-90738288	GM13976	blood:	n/a	n/a

No data

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:90735006..90737562-chr8:90957378..90959199,2	MCF-7	breast:
2	chr8:90739799..90743850-chr8:90767861..90774313,11	K562	blood:
3	chr8:90735002..90740593-chr8:90994599..90998168,11	MCF-7	breast:
4	chr8:90737986..90738708-chr8:90849422..90850036,2	MCF-7	breast:
5	chr8:90737934..90739593-chr8:90739830..90742161,2	K562	blood:
6	chr8:90740691..90742554-chr8:91012981..91015197,3	MCF-7	breast:
7	chr8:90737934..90739593-chr8:90739830..90742161,2	K562	blood:
8	chr8:90734885..90744209-chr8:90767977..90774247,14	MCF-7	breast:
9	chr8:90732925..90737686-chr8:90738407..90742912,6	K562	blood:
10	chr8:90737773..90739680-chr8:90867503..90870182,2	MCF-7	breast:
11	chr8:90736651..90739528-chr8:90739958..90742509,3	MCF-7	breast:
12	chr8:90732834..90736227-chr8:90736670..90741646,5	MCF-7	breast:
13	chr8:90737819..90738602-chr8:90996411..90997232,4	MCF-7	breast:
14	chr8:90738336..90739847-chr8:90952483..90954708,2	MCF-7	breast:
15	chr8:90740621..90743258-chr8:90763138..90765800,2	K562	blood:
16	chr8:90738912..90741485-chr8:91017416..91019883,2	K562	blood:
17	chr8:90735826..90740064-chr8:90995306..90998250,3	MCF-7	breast:
18	chr8:90737440..90740963-chr8:90912985..90916304,5	MCF-7	breast:
19	chr8:90740620..90742197-chr8:90743722..90745998,2	K562	blood:
20	chr8:90737820..90738670-chr8:90996630..90997353,4	K562	blood:
21	chr8:90734630..90736246-chr8:90739978..90742912,2	K562	blood:
22	chr8:90740411..90742010-chr8:90994882..90996914,2	K562	blood:
23	chr8:90737113..90738638-chr8:90994961..90997124,2	K562	blood:
24	chr8:90738830..90741040-chr8:90913929..90916655,2	K562	blood:
25	chr8:90714137..90717056-chr8:90737564..90740115,2	K562	blood:
26	chr8:90737750..90738653-chr8:90995891..90997375,11	MCF-7	breast:
27	chr8:90739799..90744088-chr8:90767861..90774313,10	K562	blood:
28	chr8:90736815..90743993-chr8:90765696..90773918,18	MCF-7	breast:
29	chr8:90740510..90743977-chr8:90993488..90997809,6	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NBN-1	chr8:90737746-90737871	NONHSAT127622
2	lnc-NBN-1	chr8:90736857-90737158	ENSG00000251136
3	lnc-NBN-1	chr8:90736857-90737194	NONHSAT127622
4	lnc-NBN-1	chr8:90737746-90737869	ENSG00000251136
5	lnc-NBN-1	chr8:90736857-90737194	ENSG00000251136

No data

Variant related genes	Relation type
ENSG00000251136	TF binding region
ENSG00000104320	chromatin interactions
ENSG00000251136	chromatin interactions
ENSG00000104312	chromatin interactions
ENSG00000207359	chromatin interactions
ENSG00000104325	chromatin interactions
ENSG00000164823	chromatin interactions
HMGA2	miRNA target sites
CADM1	miRNA target sites
TMEM214	miRNA target sites

Extended variants
information (count: 117 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:117 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555521378	chr8:90736958-90736959	Enhancers Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
2	rs574081134	chr8:90736959-90736960	Enhancers Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs567544069	chr8:90736961-90736962	Enhancers Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
4	rs147238336	chr8:90736970-90736971	Enhancers Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs563585552	chr8:90736980-90736981	Enhancers Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs183848095	chr8:90737018-90737019	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs73694459	chr8:90737060-90737061	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs571539586	chr8:90737132-90737133	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
9	rs538419824	chr8:90737255-90737256	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs7841459	chr8:90737258-90737259	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs528214547	chr8:90737264-90737265	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs546671668	chr8:90737336-90737337	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs565908502	chr8:90737361-90737362	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs139053387	chr8:90737380-90737381	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs149366547	chr8:90737399-90737400	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs188115236	chr8:90737402-90737403	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs550125047	chr8:90737483-90737484	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs144734315	chr8:90737500-90737501	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs554743490	chr8:90737615-90737616	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs542478916	chr8:90737647-90737648	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs11292881	chr8:90737654-90737655	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs539724329	chr8:90737721-90737722	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs369950414	chr8:90737745-90737746	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs377523554	chr8:90737803-90737804	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
25	rs55919857	chr8:90737815-90737816	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
26	rs181282000	chr8:90737898-90737899	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs534080370	chr8:90737904-90737905	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs555833679	chr8:90737905-90737906	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs3080897	chr8:90737907-90737908	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs34790922	chr8:90737910-90737911	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs199939348	chr8:90737912-90737913	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs2338846	chr8:90737913-90737914	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs2338847	chr8:90737914-90737915	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs2338848	chr8:90737915-90737916	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs574143984	chr8:90737946-90737947	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs538258938	chr8:90737948-90737949	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs116392181	chr8:90738054-90738055	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs575643041	chr8:90738055-90738056	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs550312510	chr8:90738091-90738092	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs148546209	chr8:90738140-90738141	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs11988552	chr8:90738200-90738201	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs116942927	chr8:90738206-90738207	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs561459915	chr8:90738283-90738284	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs142917723	chr8:90738284-90738285	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs547782746	chr8:90738320-90738321	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs146133661	chr8:90738372-90738373	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs140169479	chr8:90738477-90738478	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs552050971	chr8:90738496-90738497	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs567006693	chr8:90738615-90738616	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs143920986	chr8:90738707-90738708	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Autism	22495311	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
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	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
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
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:243 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90713200-90741200	Weak transcription	Left Ventricle	heart
2	chr8:90713400-90738000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr8:90713600-90756200	Weak transcription	Pancreas	Pancrea
4	chr8:90714200-90741400	Weak transcription	Right Ventricle	heart
5	chr8:90714400-90741000	Weak transcription	Gastric	stomach
6	chr8:90715400-90741200	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr8:90716800-90738000	Weak transcription	Brain Hippocampus Middle	brain
8	chr8:90717200-90741000	Weak transcription	Stomach Smooth Muscle	stomach
9	chr8:90717400-90738000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr8:90717800-90737800	Weak transcription	NHEK	skin
11	chr8:90717800-90738000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr8:90717800-90738000	Weak transcription	NH-A	brain
13	chr8:90717800-90747800	Weak transcription	Ovary	ovary
14	chr8:90720800-90742400	Weak transcription	Fetal Lung	lung
15	chr8:90721000-90740000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr8:90721400-90740400	Weak transcription	Fetal Intestine Large	intestine
17	chr8:90721800-90738400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr8:90725200-90740400	Weak transcription	Small Intestine	intestine
19	chr8:90726600-90741400	Weak transcription	Esophagus	oesophagus
20	chr8:90726800-90738200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr8:90728400-90738000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr8:90729200-90737800	Weak transcription	Fetal Heart	heart
23	chr8:90730200-90737800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr8:90731000-90738200	Weak transcription	K562	blood
25	chr8:90731000-90738400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr8:90731800-90737000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr8:90731800-90738000	Weak transcription	NHLF	lung
28	chr8:90731800-90738600	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr8:90732000-90737800	Weak transcription	Primary B cells from peripheral blood	blood
30	chr8:90732000-90737800	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr8:90732000-90737800	Weak transcription	NHDF-Ad	bronchial
32	chr8:90732000-90738200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr8:90732200-90738200	Weak transcription	HSMMtube	muscle
34	chr8:90732200-90738400	Weak transcription	HSMM	muscle
35	chr8:90733200-90738000	Weak transcription	Rectal Smooth Muscle	rectum
36	chr8:90733600-90737600	Weak transcription	A549	lung
37	chr8:90733600-90737800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr8:90733600-90737800	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr8:90733600-90737800	Weak transcription	Osteobl	bone
40	chr8:90733600-90741200	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr8:90733800-90738000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr8:90733800-90738000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr8:90734000-90737600	Weak transcription	Primary hematopoietic stem cells	blood
44	chr8:90734000-90738000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
45	chr8:90734000-90741200	Weak transcription	Liver	Liver
46	chr8:90734200-90737600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr8:90734200-90737800	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr8:90734200-90738200	Weak transcription	Aorta	Aorta
49	chr8:90734200-90738200	Weak transcription	Brain Anterior Caudate	brain
50	chr8:90734200-90739800	Weak transcription	Fetal Stomach	stomach

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