Variant report

Variant	esv3340872
Chromosome Location	chr7:149461044-149463892
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:149459407..149462884-chr7:149469034..149471281,3	MCF-7	breast:
2	chr7:149441362..149443055-chr7:149460241..149462423,2	MCF-7	breast:
3	chr7:149455232..149457688-chr7:149462668..149464925,2	MCF-7	breast:
4	chr7:149459369..149463521-chr7:149463788..149469028,7	MCF-7	breast:
5	chr7:149459369..149463521-chr7:149463788..149469028,7	MCF-7	breast:
6	chr7:149438735..149440917-chr7:149459618..149461528,2	K562	blood:
7	chr7:149448586..149450426-chr7:149459263..149461454,2	K562	blood:

Variant related genes	Relation type
ENSG00000181444	chromatin interactions

Extended variants
information (count: 144 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:144 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190080622	chr7:149461047-149461048	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs376573568	chr7:149461099-149461100	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs567765897	chr7:149461107-149461108	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs182211189	chr7:149461115-149461116	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs553307541	chr7:149461125-149461126	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs567125247	chr7:149461126-149461127	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs185593718	chr7:149461140-149461141	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs530325785	chr7:149461170-149461171	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs577210498	chr7:149461173-149461174	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs558117536	chr7:149461188-149461189	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs189484186	chr7:149461255-149461256	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs543901749	chr7:149461335-149461336	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs373244323	chr7:149461344-149461345	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs180763629	chr7:149461368-149461369	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs117383860	chr7:149461399-149461400	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs73168052	chr7:149461428-149461429	Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs73168053	chr7:149461487-149461488	Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs185205901	chr7:149461504-149461505	Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs199797137	chr7:149461506-149461507	Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs375127100	chr7:149461520-149461521	Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs371444717	chr7:149461536-149461537	Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs371111104	chr7:149461585-149461586	Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs855666	chr7:149461593-149461594	Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs565268761	chr7:149461645-149461646	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs374829113	chr7:149461657-149461658	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs530972659	chr7:149461672-149461673	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs531754070	chr7:149461694-149461695	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs10215169	chr7:149461704-149461705	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs188408041	chr7:149461732-149461733	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs199642677	chr7:149461761-149461762	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs112370637	chr7:149461774-149461775	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs566991532	chr7:149461778-149461779	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs539312457	chr7:149461833-149461834	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs558872346	chr7:149461834-149461835	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs569213675	chr7:149461835-149461836	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs371275436	chr7:149461868-149461869	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs376354036	chr7:149461869-149461870	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs376967203	chr7:149461872-149461873	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs575548240	chr7:149461873-149461874	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs554157424	chr7:149461875-149461876	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs201535763	chr7:149461895-149461896	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs574444064	chr7:149461901-149461902	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs374634951	chr7:149461912-149461913	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs368121549	chr7:149461931-149461932	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs375619721	chr7:149461941-149461942	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs201422718	chr7:149461974-149461975	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs371817253	chr7:149461975-149461976	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs374306354	chr7:149461986-149461987	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs11548976	chr7:149461987-149461988	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs11548975	chr7:149461993-149461994	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:149451000-149462400	Weak transcription	Pancreas	Pancrea
2	chr7:149451000-149462600	Weak transcription	Liver	Liver
3	chr7:149451200-149468400	Weak transcription	Right Atrium	heart
4	chr7:149451400-149461400	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr7:149452600-149463200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr7:149453000-149461600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr7:149458600-149461600	Weak transcription	Right Ventricle	heart
8	chr7:149459200-149461800	Weak transcription	Gastric	stomach
9	chr7:149459200-149462400	Weak transcription	Stomach Smooth Muscle	stomach
10	chr7:149459400-149462600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr7:149460000-149465000	Weak transcription	K562	blood
12	chr7:149460400-149462000	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr7:149460400-149463200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
14	chr7:149460400-149465400	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr7:149460600-149463200	Weak transcription	Adipose Nuclei	Adipose
16	chr7:149460600-149468200	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr7:149460800-149461200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr7:149460800-149467600	Weak transcription	Primary hematopoietic stem cells	blood
19	chr7:149460800-149467800	Strong transcription	Primary T cells from cord blood	blood
20	chr7:149461000-149461200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr7:149461000-149462400	Strong transcription	Spleen	Spleen
22	chr7:149461000-149462600	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr7:149461000-149463200	Enhancers	Esophagus	oesophagus
24	chr7:149461000-149464400	ZNF genes & repeats	Fetal Stomach	stomach
25	chr7:149461000-149467000	Strong transcription	Lung	lung
26	chr7:149461000-149467200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr7:149461000-149467800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
28	chr7:149461200-149461600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr7:149461400-149461600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
30	chr7:149461400-149461600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr7:149461400-149461600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
32	chr7:149461400-149461800	Bivalent Enhancer	Fetal Heart	heart
33	chr7:149461400-149462800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
34	chr7:149461400-149463200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
35	chr7:149461400-149463200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
36	chr7:149461400-149464200	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
37	chr7:149461600-149461800	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr7:149461600-149461800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
39	chr7:149461600-149461800	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr7:149461600-149461800	Bivalent Enhancer	Ovary	ovary
41	chr7:149461600-149462000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
42	chr7:149461600-149462000	Bivalent Enhancer	Fetal Muscle Leg	muscle
43	chr7:149461600-149462200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
44	chr7:149461600-149462200	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
45	chr7:149461600-149462400	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr7:149461600-149462400	Flanking Active TSS	Right Ventricle	heart
47	chr7:149461600-149462800	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr7:149461600-149462800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr7:149461600-149463000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
50	chr7:149461600-149463200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell

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