Variant report

Variant	esv988068
Chromosome Location	chr8:96228317-96235618
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:45)
CpG islands
(count:0)
Chromatin interactive
region (count:21)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:45 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr8:96229221-96229625	GM12878	blood:	n/a	n/a
2	CHD2	chr8:96233732-96233773	Hela-S3	cervix:	n/a	n/a
3	CHD2	chr8:96231359-96231390	HepG2	liver:	n/a	n/a
4	CTCF	chr8:96231340-96231490	HPAF	blood vessel:	n/a	n/a
5	CTCF	chr8:96231340-96231490	HUVEC	blood vessel:	n/a	n/a
6	CTCF	chr8:96231363-96231455	K562	blood:	n/a	n/a
7	CTCF	chr8:96231360-96231510	HepG2	liver:	n/a	n/a
8	CTCF	chr8:96231300-96231450	HBMEC	blood vessel:	n/a	n/a
9	CTCF	chr8:96234140-96234290	GM12864	blood:	n/a	n/a
10	EP300	chr8:96234687-96234887	K562	blood:	n/a	n/a
11	EP300	chr8:96230151-96230915	ECC-1	luminal epithelium:	n/a	n/a
12	EP300	chr8:96230515-96230520	HepG2	liver:	n/a	n/a
13	FOSL1	chr8:96235571-96235935	K562	blood:	n/a	chr8:96235846-96235857
14	FOSL2	chr8:96235532-96236411	SK-N-SH	brain:	n/a	n/a
15	FOXA1	chr8:96229945-96230272	HepG2	liver:	n/a	n/a
16	FOXA1	chr8:96229957-96230329	HepG2	liver:	n/a	n/a
17	FOXA1	chr8:96233983-96234250	T-47D	breast:	n/a	n/a
18	FOXA1	chr8:96234004-96234298	HepG2	liver:	n/a	n/a
19	FOXA2	chr8:96229921-96230242	HepG2	liver:	n/a	n/a
20	FOXA2	chr8:96234017-96234215	HepG2	liver:	n/a	n/a
21	FOXP2	chr8:96231339-96231509	PFSK-1	brain:	n/a	n/a
22	IRF1	chr8:96234572-96234890	K562	blood:	n/a	n/a
23	JUN	chr8:96235279-96236488	K562	blood:	n/a	n/a
24	JUND	chr8:96235152-96235331	K562	blood:	n/a	n/a
25	JUND	chr8:96234547-96234920	K562	blood:	n/a	n/a
26	JUND	chr8:96235482-96236348	SK-N-SH	brain:	n/a	chr8:96235846-96235857
27	JUND	chr8:96235599-96236434	K562	blood:	n/a	chr8:96235846-96235857
28	JUND	chr8:96235531-96236464	SK-N-SH	brain:	n/a	chr8:96235846-96235857
29	MAZ	chr8:96235551-96236576	Hela-S3	cervix:	n/a	n/a
30	MAZ	chr8:96234657-96234908	K562	blood:	n/a	n/a
31	MEF2A	chr8:96230373-96230822	GM12878	blood:	n/a	chr8:96230660-96230674
32	MTA3	chr8:96230420-96230924	GM12878	blood:	n/a	n/a
33	MYC	chr8:96232847-96232855	K562	blood:	n/a	n/a
34	PBX3	chr8:96229287-96229511	GM12878	blood:	n/a	n/a
35	POLR2A	chr8:96232115-96232646	K562	blood:	n/a	n/a
36	RCOR1	chr8:96234620-96235210	K562	blood:	n/a	n/a
37	RCOR1	chr8:96228060-96228351	K562	blood:	n/a	n/a
38	RCOR1	chr8:96234747-96234805	K562	blood:	n/a	n/a
39	RUNX3	chr8:96230287-96230721	GM12878	blood:	n/a	n/a
40	SMC3	chr8:96230534-96230628	GM12878	blood:	n/a	n/a
41	UBTF	chr8:96231313-96231427	K562	blood:	n/a	n/a
42	USF2	chr8:96231406-96231508	H1-hESC	embryonic stem cell:	n/a	n/a
43	ZC3H11A	chr8:96232064-96232151	K562	blood:	n/a	n/a
44	ZNF143	chr8:96234498-96234503	K562	blood:	n/a	n/a
45	ZNF143	chr8:96231260-96231465	H1-hESC	embryonic stem cell:	n/a	chr8:96231354-96231373

No data

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:96228952..96231247-chr8:96237951..96240683,3	MCF-7	breast:
2	chr8:96143360..96148175-chr8:96235522..96240876,10	MCF-7	breast:
3	chr8:96111749..96114066-chr8:96234612..96236782,2	K562	blood:
4	chr8:96230420..96235229-chr8:96280327..96282960,4	MCF-7	breast:
5	chr8:96229120..96231629-chr8:96232251..96235212,3	MCF-7	breast:
6	chr8:96077808..96080245-chr8:96234205..96235808,2	MCF-7	breast:
7	chr8:96232323..96234888-chr8:96235835..96240054,4	MCF-7	breast:
8	chr8:96214009..96217041-chr8:96227079..96229399,3	K562	blood:
9	chr8:96222030..96225621-chr8:96235538..96238037,4	MCF-7	breast:
10	chr8:96231573..96233965-chr8:96249378..96252236,2	K562	blood:
11	chr8:96233041..96235359-chr8:96238288..96241007,3	K562	blood:
12	chr8:96145268..96146858-chr8:96230035..96232960,2	MCF-7	breast:
13	chr8:96229389..96231464-chr8:96247771..96249721,2	K562	blood:
14	chr8:96148421..96149927-chr8:96235607..96238590,2	K562	blood:
15	chr8:96234981..96237972-chr8:97273758..97275615,2	MCF-7	breast:
16	chr8:96229120..96231629-chr8:96232251..96235212,3	MCF-7	breast:
17	chr8:96204685..96206421-chr8:96234538..96236078,2	MCF-7	breast:
18	chr8:96222002..96228732-chr8:96228964..96237755,16	MCF-7	breast:
19	chr8:96147448..96150087-chr8:96233164..96235373,2	MCF-7	breast:
20	chr8:96232022..96234358-chr8:96242400..96245249,2	K562	blood:
21	chr8:96234462..96239842-chr8:96279058..96283088,6	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf37-1	chr8:96228546-96228743	NONHSAT127827
2	lnc-C8orf37-1	chr8:96228546-96228602	ENSG00000253351

No data

Variant related genes	Relation type
ENSG00000253351	TF binding region
ENSG00000156469	chromatin interactions
ENSG00000156471	chromatin interactions
ENSG00000175895	chromatin interactions
ENSG00000253351	chromatin interactions
ENSG00000253773	chromatin interactions
ENSG00000156172	chromatin interactions
ENSG00000156170	chromatin interactions

Extended variants
information (count: 291 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:291 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374906846	chr8:96228322-96228323	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs186765946	chr8:96228354-96228355	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs576609922	chr8:96228367-96228368	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs13261934	chr8:96228372-96228373	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs115523396	chr8:96228385-96228386	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs192637635	chr8:96228388-96228389	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs565622188	chr8:96228393-96228394	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs527674265	chr8:96228436-96228437	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs185633046	chr8:96228454-96228455	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs139044079	chr8:96228459-96228460	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs553071524	chr8:96228471-96228472	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs530154274	chr8:96228472-96228473	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs550286086	chr8:96228476-96228477	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs386727922	chr8:96228479-96228480	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs77528915	chr8:96228481-96228482	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs190495296	chr8:96228491-96228492	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs150948809	chr8:96228533-96228534	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs554213597	chr8:96228567-96228568	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs372828587	chr8:96228601-96228602	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs533500091	chr8:96228611-96228612	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs140848675	chr8:96228635-96228636	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs573645413	chr8:96228649-96228650	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs149713639	chr8:96228655-96228656	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs556251590	chr8:96228670-96228671	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs576558087	chr8:96228696-96228697	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs540552324	chr8:96228795-96228796	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs571973149	chr8:96228800-96228801	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs112864309	chr8:96228823-96228824	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs377645036	chr8:96228889-96228890	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs541024706	chr8:96228908-96228909	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs181748177	chr8:96228977-96228978	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs376018000	chr8:96229125-96229126	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs78063021	chr8:96229163-96229164	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs561112217	chr8:96229164-96229165	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs62522650	chr8:96229165-96229166	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs145674269	chr8:96229177-96229178	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs550005760	chr8:96229232-96229233	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs28377810	chr8:96229270-96229271	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs531363589	chr8:96229300-96229301	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs60018559	chr8:96229325-96229326	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs199926979	chr8:96229370-96229371	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs372047996	chr8:96229374-96229375	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs369273794	chr8:96229388-96229389	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs28673830	chr8:96229436-96229437	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs200373871	chr8:96229494-96229495	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs547321583	chr8:96229522-96229523	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs532888113	chr8:96229564-96229565	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs536291898	chr8:96229570-96229571	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs184357476	chr8:96229575-96229576	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs569739070	chr8:96229587-96229588	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:110)

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
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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96214400-96233400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr8:96219400-96229600	Enhancers	Fetal Thymus	thymus
3	chr8:96219800-96251800	Enhancers	Primary B cells from peripheral blood	blood
4	chr8:96220600-96229400	Enhancers	Primary hematopoietic stem cells	blood
5	chr8:96220800-96229600	Enhancers	Primary B cells from cord blood	blood
6	chr8:96221000-96228400	Enhancers	Primary T cells fromperipheralblood	blood
7	chr8:96221200-96228800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr8:96222000-96228400	Enhancers	Primary T cells from cord blood	blood
9	chr8:96223200-96228600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr8:96223600-96237200	Weak transcription	Fetal Intestine Small	intestine
11	chr8:96223800-96228800	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr8:96223800-96229200	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr8:96224000-96228800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr8:96224200-96230000	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr8:96224600-96228400	Enhancers	Spleen	Spleen
16	chr8:96225200-96229800	Weak transcription	Stomach Mucosa	stomach
17	chr8:96225400-96228800	Weak transcription	HepG2	liver
18	chr8:96225400-96232800	Weak transcription	Esophagus	oesophagus
19	chr8:96225600-96236200	Weak transcription	Gastric	stomach
20	chr8:96226000-96228800	Enhancers	Fetal Muscle Leg	muscle
21	chr8:96226400-96228800	Enhancers	Left Ventricle	heart
22	chr8:96226400-96229400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr8:96226600-96231800	Enhancers	K562	blood
24	chr8:96226800-96230000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr8:96227000-96231200	Weak transcription	Psoas Muscle	Psoas
26	chr8:96227000-96232400	Weak transcription	Pancreas	Pancrea
27	chr8:96227200-96230200	Weak transcription	Fetal Heart	heart
28	chr8:96227400-96228600	Weak transcription	Liver	Liver
29	chr8:96227400-96229000	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr8:96227400-96230400	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr8:96227400-96232800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr8:96227400-96233600	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr8:96227600-96228400	Enhancers	Brain Hippocampus Middle	brain
34	chr8:96227600-96229000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr8:96227600-96229600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr8:96227600-96230200	Weak transcription	GM12878-XiMat	blood
37	chr8:96227600-96231200	Weak transcription	Adipose Nuclei	Adipose
38	chr8:96227600-96231200	Weak transcription	Right Ventricle	heart
39	chr8:96227600-96231600	Weak transcription	Right Atrium	heart
40	chr8:96227600-96232800	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr8:96227800-96230400	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr8:96227800-96233000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr8:96228000-96229800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr8:96228000-96238800	Weak transcription	Thymus	Thymus
45	chr8:96228200-96228800	Enhancers	Placenta	Placenta
46	chr8:96228200-96229000	Enhancers	Aorta	Aorta
47	chr8:96228400-96230200	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr8:96228400-96231200	Weak transcription	Spleen	Spleen
49	chr8:96228400-96232200	Weak transcription	Primary T cells from cord blood	blood
50	chr8:96228600-96228800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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