Variant report

Variant	esv1849780
Chromosome Location	chr1:114577463-114663164
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:169)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:169 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr1:114591094..114593001-chr1:114597614..114600452,2	K562	blood:
2	chr1:114621189..114624161-chr1:114624603..114627561,2	MCF-7	breast:
3	chr1:114590926..114593498-chr1:114625359..114627730,2	MCF-7	breast:
4	chr1:114636244..114636762-chr1:114828230..114828909,2	MCF-7	breast:
5	chr1:114644709..114646503-chr1:114655020..114657132,2	MCF-7	breast:
6	chr1:114615333..114617366-chr1:114618572..114622103,3	MCF-7	breast:
7	chr1:114648677..114650215-chr1:115123817..115125650,2	MCF-7	breast:
8	chr1:114628179..114629979-chr1:114633594..114635388,2	K562	blood:
9	chr1:114595497..114597013-chr1:114615849..114618370,2	MCF-7	breast:
10	chr1:114595324..114597061-chr1:114598670..114600429,2	K562	blood:
11	chr1:114647802..114648660-chr16:67189250..67189815,2	MCF-7	breast:
12	chr1:114647200..114648760-chr1:114757392..114758723,8	MCF-7	breast:
13	chr1:114622978..114624850-chr1:114631816..114634562,2	K562	blood:
14	chr1:114619893..114621772-chr1:114628579..114631100,2	K562	blood:
15	chr1:114629056..114630964-chr22:38054441..38056208,2	MCF-7	breast:
16	chr1:114635795..114636351-chr16:67189024..67189884,2	MCF-7	breast:
17	chr1:114635893..114636419-chr1:114761811..114762721,2	MCF-7	breast:
18	chr1:114621187..114625954-chr1:114630932..114635442,7	MCF-7	breast:
19	chr1:114596275..114599885-chr1:114602118..114604793,4	MCF-7	breast:
20	chr1:114587184..114588685-chr1:114594720..114597075,2	MCF-7	breast:
21	chr1:114635753..114636625-chr1:114758689..114759431,2	MCF-7	breast:
22	chr1:114520498..114523229-chr1:114575695..114578071,3	MCF-7	breast:
23	chr1:114623967..114627228-chr1:114653926..114657100,3	K562	blood:
24	chr1:114543887..114546791-chr1:114577396..114579805,2	MCF-7	breast:
25	chr1:114577897..114580371-chr1:114581560..114584344,2	MCF-7	breast:
26	chr1:114623682..114625448-chr1:114629138..114631604,2	K562	blood:
27	chr1:114596275..114599885-chr1:114602118..114604793,4	MCF-7	breast:
28	chr1:114653590..114655647-chr1:114659608..114662763,3	MCF-7	breast:
29	chr1:114574403..114579108-chr1:114596233..114599527,4	MCF-7	breast:
30	chr1:114650119..114651429-chr1:114825151..114826103,7	MCF-7	breast:
31	chr1:114614196..114617663-chr1:114624428..114628635,5	MCF-7	breast:
32	chr1:114633144..114634920-chr1:114648218..114649973,2	MCF-7	breast:
33	chr1:114621189..114624161-chr1:114624603..114627561,2	MCF-7	breast:
34	chr1:114635981..114636840-chr1:114825182..114826118,4	MCF-7	breast:
35	chr1:114657028..114661761-chr1:114663955..114667421,5	MCF-7	breast:
36	chr1:114653542..114655254-chr1:114680664..114683283,2	K562	blood:
37	chr1:114621614..114625641-chr1:114627637..114630642,5	MCF-7	breast:
38	chr1:114642020..114643527-chr1:114656565..114659133,2	MCF-7	breast:
39	chr1:114623758..114625854-chr1:114633416..114636156,2	MCF-7	breast:
40	chr1:114577056..114579380-chr1:114582977..114584723,3	MCF-7	breast:
41	chr1:114521456..114522097-chr1:114635919..114636683,3	MCF-7	breast:
42	chr1:114609946..114612096-chr1:114617825..114619412,2	MCF-7	breast:
43	chr1:114657401..114660243-chr1:114668370..114670843,2	MCF-7	breast:
44	chr1:114565136..114566738-chr1:114579035..114581815,2	MCF-7	breast:
45	chr1:114534979..114536505-chr1:114575410..114577560,2	MCF-7	breast:
46	chr1:114632835..114634373-chr1:114642093..114644648,2	MCF-7	breast:
47	chr1:114594344..114596530-chr1:114631234..114632774,2	MCF-7	breast:
48	chr1:114647297..114648035-chr1:114824902..114825987,5	MCF-7	breast:
49	chr1:114614196..114617663-chr1:114624428..114628635,5	MCF-7	breast:
50	chr1:114585530..114588046-chr1:114622243..114625192,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OLFML3-3	chr1:114606351-114606423	NONHSAT005349
2	lnc-OLFML3-2	chr1:114577818-114578381	NONHSAT005352

No data

Variant related genes	Relation type
ENSG00000116774	chromatin interactions
ENSG00000102871	chromatin interactions
ENSG00000135722	chromatin interactions
ENSG00000101040	chromatin interactions
ENSG00000241360	chromatin interactions
ENSG00000116752	chromatin interactions
ENSG00000134262	chromatin interactions
ENSG00000270780	chromatin interactions
ENSG00000134207	chromatin interactions

Extended variants
information (count: 3481 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:3481 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115777704	chr1:114577480-114577481	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs185716289	chr1:114577496-114577497	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs566221487	chr1:114577498-114577499	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs534918908	chr1:114577501-114577502	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs576056300	chr1:114577509-114577510	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs578162446	chr1:114577510-114577511	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs537437421	chr1:114577538-114577539	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs557430485	chr1:114577558-114577559	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs2938340	chr1:114577595-114577596	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs191801425	chr1:114577601-114577602	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs17032146	chr1:114577608-114577609	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs183626701	chr1:114577614-114577615	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs4839003	chr1:114577615-114577616	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs564616819	chr1:114577635-114577636	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs374952756	chr1:114577662-114577663	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs540273101	chr1:114577663-114577664	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs142876873	chr1:114577740-114577741	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs373873869	chr1:114577761-114577762	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs564836825	chr1:114577771-114577772	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs188181914	chr1:114577781-114577782	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs547535103	chr1:114577801-114577802	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs12740538	chr1:114577829-114577830	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs75776714	chr1:114577917-114577918	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs192774950	chr1:114577972-114577973	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs79228094	chr1:114578009-114578010	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs146100149	chr1:114578065-114578066	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs138859652	chr1:114578066-114578067	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs552048182	chr1:114578072-114578073	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs182700472	chr1:114578076-114578077	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs78624024	chr1:114578092-114578093	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs545835866	chr1:114578121-114578122	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs371901920	chr1:114578127-114578128	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs17466149	chr1:114578153-114578154	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs573950001	chr1:114578167-114578168	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs186801261	chr1:114578243-114578244	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs376577846	chr1:114578252-114578253	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs553216758	chr1:114578287-114578288	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs573083782	chr1:114578310-114578311	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs544800807	chr1:114578326-114578327	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs555914697	chr1:114578338-114578339	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs150877924	chr1:114578346-114578347	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs571213381	chr1:114578369-114578370	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs115203007	chr1:114578370-114578371	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs560673454	chr1:114578411-114578412	Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs60727700	chr1:114578412-114578413	Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs368244805	chr1:114578436-114578437	Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs575886067	chr1:114578619-114578620	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs75650075	chr1:114578650-114578651	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs559990863	chr1:114578656-114578657	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs10494165	chr1:114578735-114578736	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Asthma	20841430	CNVD
Aetanephric adenomas	20802469	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	21956041	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	16573809	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Breast cancer	17899364	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Melanoma	19671679	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1010 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:114575000-114577600	Enhancers	HMEC	breast
2	chr1:114575000-114577800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
3	chr1:114575000-114578000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
4	chr1:114575000-114578400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
5	chr1:114575000-114578400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr1:114575200-114578400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
7	chr1:114575400-114577600	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr1:114575800-114577800	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr1:114576000-114577600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr1:114576000-114577800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:114576000-114579400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:114576000-114580200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr1:114576000-114582800	Weak transcription	HSMMtube	muscle
14	chr1:114576000-114583400	Weak transcription	Lung	lung
15	chr1:114576400-114577600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr1:114576400-114579000	Weak transcription	Fetal Muscle Leg	muscle
17	chr1:114576600-114580400	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr1:114576600-114582800	Weak transcription	Fetal Intestine Large	intestine
19	chr1:114576800-114578400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
20	chr1:114576800-114578800	Weak transcription	Fetal Intestine Small	intestine
21	chr1:114577000-114578200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
22	chr1:114577000-114580800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr1:114577200-114577600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr1:114577200-114578000	Flanking Active TSS	H1 Cell Line	embryonic stem cell
25	chr1:114577200-114580600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr1:114577200-114583200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr1:114577400-114577600	Flanking Active TSS	H9 Cell Line	embryonic stem cell
28	chr1:114577400-114577800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr1:114577400-114578800	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr1:114577400-114580800	Weak transcription	NHEK	skin
31	chr1:114577400-114582000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr1:114577600-114577800	Active TSS	H9 Cell Line	embryonic stem cell
33	chr1:114577600-114578000	Flanking Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr1:114577600-114578000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr1:114577600-114579000	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr1:114577600-114580200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr1:114577600-114580800	Weak transcription	HMEC	breast
38	chr1:114577800-114578200	Flanking Active TSS	H9 Cell Line	embryonic stem cell
39	chr1:114577800-114578200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr1:114577800-114578600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
41	chr1:114577800-114583000	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr1:114578000-114578200	Enhancers	H1 Cell Line	embryonic stem cell
43	chr1:114578000-114579000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr1:114578000-114580200	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr1:114578000-114582200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr1:114578200-114578600	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr1:114578200-114578600	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr1:114578200-114579000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr1:114578200-114583000	Enhancers	H9 Cell Line	embryonic stem cell
50	chr1:114578400-114579400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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