Variant report

Variant	esv992888
Chromosome Location	chr11:64624637-64626194
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	BCLAF1	chr11:64626107-64626729	GM12878	blood:	n/a	n/a
2	BHLHE40	chr11:64626178-64626607	GM12878	blood:	n/a	n/a
3	CEBPB	chr11:64623934-64624696	A549	lung:	n/a	n/a
4	CEBPB	chr11:64623832-64624780	HCT-116	colon:	n/a	n/a
5	CTCF	chr11:64626120-64626270	GM12872	blood:	n/a	chr11:64626215-64626228 chr11:64626219-64626228
6	EBF1	chr11:64625950-64627591	GM12878	blood:	n/a	n/a
7	ELF1	chr11:64625854-64626778	GM12878	blood:	n/a	n/a
8	ELF1	chr11:64624864-64625504	GM12878	blood:	n/a	n/a
9	EP300	chr11:64625991-64626525	GM12878	blood:	n/a	n/a
10	FOS	chr11:64626114-64626169	MCF10A-Er-Src	breast:	n/a	n/a
11	GATA3	chr11:64623866-64624647	A549	lung:	n/a	n/a
12	GTF2F1	chr11:64625147-64625240	Hela-S3	cervix:	n/a	n/a
13	IRF3	chr11:64625297-64625304	GM12878	blood:	n/a	n/a
14	JUND	chr11:64623755-64624670	HCT-116	colon:	n/a	chr11:64624318-64624328 chr11:64624320-64624331 chr11:64624318-64624328 chr11:64624317-64624328 chr11:64624319-64624327 chr11:64624318-64624328 chr11:64624318-64624328
15	MAX	chr11:64623584-64624782	HCT-116	colon:	n/a	n/a
16	MAX	chr11:64623678-64624641	HCT-116	colon:	n/a	n/a
17	MAX	chr11:64626059-64626194	Hela-S3	cervix:	n/a	n/a
18	MAX	chr11:64623681-64624703	A549	lung:	n/a	n/a
19	MAX	chr11:64623520-64624717	A549	lung:	n/a	n/a
20	MAZ	chr11:64621773-64624673	IMR90	lung:	n/a	chr11:64622332-64622342
21	MTA3	chr11:64623486-64624710	GM12878	blood:	n/a	n/a
22	MTA3	chr11:64624929-64625679	GM12878	blood:	n/a	n/a
23	MTA3	chr11:64625827-64627988	GM12878	blood:	n/a	n/a
24	MTA3	chr11:64625974-64626658	GM12878	blood:	n/a	n/a
25	MXI1	chr11:64623859-64624708	IMR90	lung:	n/a	n/a
26	NFATC1	chr11:64625931-64626723	GM12878	blood:	n/a	n/a
27	NR2F2	chr11:64625902-64626193	K562	blood:	n/a	n/a
28	NR3C1	chr11:64624137-64624683	A549	lung:	n/a	chr11:64624319-64624328 chr11:64624318-64624327
29	NR3C1	chr11:64623975-64624751	A549	lung:	n/a	chr11:64624319-64624328 chr11:64624318-64624327
30	PAX5	chr11:64625895-64627521	GM12878	blood:	n/a	n/a
31	PBX3	chr11:64626014-64626183	GM12878	blood:	n/a	chr11:64626118-64626127
32	PBX3	chr11:64625983-64626232	GM12878	blood:	n/a	chr11:64626118-64626127
33	PML	chr11:64625805-64627653	GM12878	blood:	n/a	n/a
34	PML	chr11:64623652-64624677	GM12878	blood:	n/a	chr11:64624543-64624551 chr11:64624317-64624326
35	POLR2A	chr11:64625769-64628340	GM12892	blood:	n/a	n/a
36	POLR2A	chr11:64625891-64626663	GM12891	blood:	n/a	n/a
37	POLR2A	chr11:64624930-64625464	GM12891	blood:	n/a	n/a
38	POLR2A	chr11:64615602-64624722	GM12892	blood:	n/a	n/a
39	POLR2A	chr11:64626076-64626265	HUVEC	blood vessel:	n/a	n/a
40	POLR2A	chr11:64618326-64624803	U87	brain:	n/a	n/a
41	POLR2A	chr11:64625809-64628309	GM12878	blood:	n/a	n/a
42	POLR2A	chr11:64624910-64625452	Hela-S3	cervix:	n/a	n/a
43	POLR2A	chr11:64624911-64625473	GM12878	blood:	n/a	n/a
44	POLR2A	chr11:64624913-64625488	GM12892	blood:	n/a	n/a
45	POLR2A	chr11:64626067-64626867	GM12878	blood:	n/a	n/a
46	POLR2A	chr11:64621078-64624649	GM12891	blood:	n/a	n/a
47	POLR2A	chr11:64625833-64626782	GM12891	blood:	n/a	n/a
48	POLR2A	chr11:64625368-64625390	GM12878	blood:	n/a	n/a
49	POLR2A	chr11:64625883-64626449	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr11:64615614-64641325	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:64544849..64546824-chr11:64622424..64625371,2	K562	blood:
2	chr11:64544849..64546983-chr11:64621402..64625371,3	K562	blood:
3	11:64620201-64626490..11:64658316-64660295	Hela-S3	cervix:

Variant related genes	Relation type
EHD1	TF binding region
ENSG00000269038	chromatin interactions
ENSG00000229719	chromatin interactions
ENSG00000168066	chromatin interactions
ENSG00000207648	chromatin interactions
ENSG00000267804	chromatin interactions

Extended variants
information (count: 61 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:61 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535334214	chr11:64624644-64624645	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs549147832	chr11:64624694-64624695	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs183230124	chr11:64624714-64624715	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs568489567	chr11:64624763-64624764	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs376568032	chr11:64624769-64624770	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs537515562	chr11:64624832-64624833	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs557408134	chr11:64624840-64624841	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs577269728	chr11:64624852-64624853	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs541262008	chr11:64624855-64624856	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs188002134	chr11:64624879-64624880	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs144730780	chr11:64624944-64624945	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs7926812	chr11:64624953-64624954	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs573467131	chr11:64624962-64624963	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs542085590	chr11:64624966-64624967	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs138684288	chr11:64624981-64624982	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs577835300	chr11:64624992-64624993	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs78876565	chr11:64624999-64625000	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs376151841	chr11:64625009-64625010	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs543102638	chr11:64625094-64625095	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs543862263	chr11:64625098-64625099	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs563740247	chr11:64625102-64625103	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs369611070	chr11:64625188-64625189	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs7952567	chr11:64625282-64625283	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs546567668	chr11:64625285-64625286	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs560225482	chr11:64625331-64625332	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs529166764	chr11:64625361-64625362	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs374965531	chr11:64625371-64625372	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs548928708	chr11:64625450-64625451	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs528923036	chr11:64625455-64625456	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs79034234	chr11:64625485-64625486	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs551048234	chr11:64625490-64625491	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs544679835	chr11:64625499-64625500	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs11327531	chr11:64625510-64625511	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs570947060	chr11:64625532-64625533	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs35570847	chr11:64625535-64625536	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs539482492	chr11:64625558-64625559	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs369089907	chr11:64625634-64625635	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs112938802	chr11:64625639-64625640	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs56333212	chr11:64625662-64625663	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs35845027	chr11:64625667-64625668	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs398016403	chr11:64625671-64625672	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs7927560	chr11:64625709-64625710	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs191129524	chr11:64625733-64625734	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs555688533	chr11:64625756-64625757	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs376055345	chr11:64625789-64625790	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs564339246	chr11:64625794-64625795	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs544396783	chr11:64625811-64625812	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs377752923	chr11:64625814-64625815	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs563880860	chr11:64625819-64625820	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs35723149	chr11:64625854-64625855	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Prostate cancer	18779856	CNVD
Cancer	17160897	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:204 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64612600-64639000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr11:64613000-64629800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:64613000-64630600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr11:64617200-64627600	Genic enhancers	Fetal Intestine Small	intestine
5	chr11:64617200-64627600	Genic enhancers	NHLF	lung
6	chr11:64617600-64629600	Weak transcription	Fetal Brain Male	brain
7	chr11:64618600-64626200	Genic enhancers	Primary T cells fromperipheralblood	blood
8	chr11:64618600-64626200	Genic enhancers	Thymus	Thymus
9	chr11:64618600-64628000	Genic enhancers	Fetal Intestine Large	intestine
10	chr11:64618800-64627800	Strong transcription	Brain Germinal Matrix	brain
11	chr11:64618800-64627800	Strong transcription	Fetal Brain Female	brain
12	chr11:64618800-64627800	Genic enhancers	Fetal Muscle Leg	muscle
13	chr11:64619000-64625400	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr11:64619000-64626600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr11:64619000-64627800	Genic enhancers	Sigmoid Colon	Sigmoid Colon
16	chr11:64619000-64628200	Genic enhancers	Fetal Muscle Trunk	muscle
17	chr11:64619200-64626200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr11:64619200-64626400	Genic enhancers	Fetal Thymus	thymus
19	chr11:64619200-64626400	Genic enhancers	Gastric	stomach
20	chr11:64619200-64627800	Genic enhancers	Adipose Nuclei	Adipose
21	chr11:64619200-64628000	Strong transcription	Cortex derived primary cultured neurospheres	brain
22	chr11:64619200-64628000	Genic enhancers	Spleen	Spleen
23	chr11:64619200-64630200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr11:64619400-64626600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr11:64619400-64626600	Genic enhancers	HMEC	breast
26	chr11:64619600-64626200	Genic enhancers	Liver	Liver
27	chr11:64619800-64626400	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
28	chr11:64619800-64628000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr11:64619800-64628000	Genic enhancers	Right Ventricle	heart
30	chr11:64619800-64632400	Genic enhancers	Primary B cells from peripheral blood	blood
31	chr11:64620000-64625200	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr11:64620400-64625400	Enhancers	Psoas Muscle	Psoas
33	chr11:64620800-64625200	Enhancers	HUVEC	blood vessel
34	chr11:64620800-64626400	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr11:64620800-64627800	Genic enhancers	Esophagus	oesophagus
36	chr11:64620800-64628200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr11:64620800-64630200	Weak transcription	Fetal Kidney	kidney
38	chr11:64621400-64625200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr11:64621400-64625800	Genic enhancers	Primary T helper cells fromperipheralblood	blood
40	chr11:64621600-64625200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr11:64621600-64625400	Genic enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr11:64621600-64626200	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr11:64621800-64625400	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr11:64621800-64626000	Genic enhancers	GM12878-XiMat	blood
45	chr11:64621800-64627600	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr11:64621800-64627800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr11:64621800-64628000	Enhancers	Right Atrium	heart
48	chr11:64622000-64624800	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr11:64622000-64626400	Enhancers	Small Intestine	intestine
50	chr11:64622200-64625000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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