Variant report

Variant	nsv438037
Chromosome Location	chr1:152079989-152084039
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:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type
1	chr1:152014593..152017230-chr1:152082456..152084502,3	MCF-7	breast:
2	chr1:152078746..152081209-chr1:152082799..152085441,3	K562	blood:
3	chr1:152039144..152040996-chr1:152081393..152082940,2	MCF-7	breast:
4	chr1:152020825..152023230-chr1:152081998..152084966,2	MCF-7	breast:
5	chr1:152042308..152047029-chr1:152081777..152083465,4	MCF-7	breast:
6	chr1:152019653..152021946-chr1:152081458..152082982,2	MCF-7	breast:
7	chr1:152007161..152009536-chr1:152080414..152082026,2	MCF-7	breast:
8	chr1:152078746..152081209-chr1:152082799..152085441,3	K562	blood:
9	chr1:152083017..152085583-chr1:152100837..152102979,2	MCF-7	breast:
10	chr1:152058557..152062058-chr1:152082903..152085603,4	MCF-7	breast:
11	chr1:152083046..152085813-chr1:152103196..152106111,3	MCF-7	breast:
12	chr1:152073757..152075757-chr1:152077578..152080436,2	K562	blood:
13	chr1:152008020..152010755-chr1:152080954..152084659,4	MCF-7	breast:
14	chr1:152054917..152058416-chr1:152081485..152084438,3	MCF-7	breast:
15	chr1:152082126..152084401-chr1:152135416..152137252,2	MCF-7	breast:
16	chr1:152082811..152085581-chr1:152092472..152094632,2	MCF-7	breast:
17	chr1:152018511..152020691-chr1:152081107..152083275,2	MCF-7	breast:
18	chr1:152064256..152066626-chr1:152081752..152084495,3	MCF-7	breast:
19	chr1:152025430..152028089-chr1:152082094..152084802,2	MCF-7	breast:
20	chr1:152023393..152025689-chr1:152081392..152083739,7	MCF-7	breast:
21	chr1:152081901..152084932-chr1:152421607..152423575,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000182898	chromatin interactions
ENSG00000163191	chromatin interactions

Extended variants
information (count: 384 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:384 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1131471	chr1:152079989-152079990	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs200484504	chr1:152080007-152080008	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532342360	chr1:152080008-152080009	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs146665414	chr1:152080012-152080013	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs374186199	chr1:152080026-152080027	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs201952511	chr1:152080033-152080034	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs140720320	chr1:152080066-152080067	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs534079109	chr1:152080073-152080074	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs558816246	chr1:152080075-152080076	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577108204	chr1:152080096-152080097	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs201552909	chr1:152080105-152080106	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528411502	chr1:152080116-152080117	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs367821937	chr1:152080117-152080118	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs371303479	chr1:152080121-152080122	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs199722465	chr1:152080123-152080124	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs144466953	chr1:152080129-152080130	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536655370	chr1:152080139-152080140	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535325232	chr1:152080155-152080156	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs201647177	chr1:152080160-152080161	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368495817	chr1:152080166-152080167	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200261270	chr1:152080173-152080174	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs375634775	chr1:152080175-152080176	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs369730040	chr1:152080179-152080180	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs371824808	chr1:152080206-152080207	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs550260117	chr1:152080228-152080229	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376831805	chr1:152080241-152080242	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs368815102	chr1:152080247-152080248	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570255654	chr1:152080255-152080256	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs2496248	chr1:152080257-152080258	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs201148604	chr1:152080271-152080272	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs202089738	chr1:152080283-152080284	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs373052740	chr1:152080295-152080296	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs377741532	chr1:152080301-152080302	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs369831201	chr1:152080321-152080322	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559135114	chr1:152080326-152080327	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs2515667	chr1:152080347-152080348	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs2496249	chr1:152080348-152080349	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs199599922	chr1:152080354-152080355	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs373841793	chr1:152080360-152080361	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs71625146	chr1:152080372-152080373	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs71585885	chr1:152080383-152080384	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs371137520	chr1:152080387-152080388	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs372988346	chr1:152080406-152080407	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs71585886	chr1:152080414-152080415	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs572574767	chr1:152080422-152080423	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs201312296	chr1:152080426-152080427	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs370174946	chr1:152080441-152080442	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs535291908	chr1:152080509-152080510	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs146612508	chr1:152080512-152080513	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs368704617	chr1:152080533-152080534	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:123)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:521 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:152079600-152080200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
2	chr1:152079800-152080000	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:152079800-152080000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:152079800-152080000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr1:152079800-152080000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr1:152079800-152080000	Enhancers	Pancreas	Pancrea
7	chr1:152079800-152080000	Flanking Bivalent TSS/Enh	A549	lung
8	chr1:152079800-152080000	Bivalent Enhancer	HMEC	breast
9	chr1:152079800-152080000	Bivalent Enhancer	NHDF-Ad	bronchial
10	chr1:152079800-152080200	Bivalent/Poised TSS	Muscle Satellite Cultured Cells	--
11	chr1:152079800-152080200	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
12	chr1:152079800-152080200	Flanking Bivalent TSS/Enh	NHEK	skin
13	chr1:152079800-152080400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
14	chr1:152079800-152080400	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
15	chr1:152079800-152080400	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
16	chr1:152079800-152080400	Flanking Bivalent TSS/Enh	Placenta	Placenta
17	chr1:152079800-152080600	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
18	chr1:152079800-152080800	Enhancers	Gastric	stomach
19	chr1:152079800-152081200	Flanking Bivalent TSS/Enh	HUVEC	blood vessel
20	chr1:152079800-152081400	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr1:152079800-152081600	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr1:152079800-152081800	ZNF genes & repeats	Aorta	Aorta
23	chr1:152079800-152082000	Bivalent/Poised TSS	Brain Substantia Nigra	brain
24	chr1:152079800-152082200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
25	chr1:152079800-152082800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr1:152079800-152083000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
27	chr1:152079800-152083200	ZNF genes & repeats	Lung	lung
28	chr1:152079800-152084400	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr1:152079800-152085400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr1:152079800-152085400	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
31	chr1:152080000-152080200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
32	chr1:152080000-152080200	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr1:152080000-152080200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
34	chr1:152080000-152080200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr1:152080000-152080200	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr1:152080000-152080200	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
37	chr1:152080000-152080200	Bivalent Enhancer	Spleen	Spleen
38	chr1:152080000-152080400	Flanking Bivalent TSS/Enh	Esophagus	oesophagus
39	chr1:152080000-152080400	Bivalent Enhancer	Left Ventricle	heart
40	chr1:152080000-152081000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr1:152080000-152081000	Bivalent/Poised TSS	A549	lung
42	chr1:152080000-152081200	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr1:152080000-152081200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
44	chr1:152080000-152081200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
45	chr1:152080000-152081200	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr1:152080000-152081400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
47	chr1:152080000-152081400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr1:152080000-152081400	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
49	chr1:152080000-152081600	ZNF genes & repeats	Pancreas	Pancrea
50	chr1:152080000-152081600	ZNF genes & repeats	Right Atrium	heart

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