Variant report

Variant	esv3433859
Chromosome Location	chr9:102589981-102592279
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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:102581880..102584384-chr9:102587876..102590490,2	MCF-7	breast:
2	chr9:102582180..102584065-chr9:102591748..102594566,2	MCF-7	breast:
3	chr9:102592088..102595529-chr9:102596867..102600515,3	K562	blood:
4	chr9:102587323..102589570-chr9:102589778..102591826,2	MCF-7	breast:
5	chr9:102590542..102592344-chr9:102611716..102613330,2	K562	blood:
6	chr9:102589376..102591940-chr9:102594219..102596621,2	MCF-7	breast:
7	chr9:102584717..102589672-chr9:102590692..102593827,7	K562	blood:
8	chr9:102581904..102584388-chr9:102591286..102592818,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000119508	chromatin interactions
ENSG00000237461	chromatin interactions

Extended variants
information (count: 71 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:71 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545955202	chr9:102589993-102589994	Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs564374578	chr9:102589996-102589997	Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs531862737	chr9:102590063-102590064	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs35491020	chr9:102590123-102590124	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs530413886	chr9:102590222-102590223	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs543811833	chr9:102590281-102590282	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs201656934	chr9:102590344-102590345	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs184308000	chr9:102590366-102590367	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs546710870	chr9:102590378-102590379	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs376617366	chr9:102590396-102590397	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs369623121	chr9:102590402-102590403	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs375331559	chr9:102590412-102590413	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs200361772	chr9:102590436-102590437	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs143302255	chr9:102590472-102590473	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs529538777	chr9:102590482-102590483	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs150301488	chr9:102590503-102590504	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs549690634	chr9:102590508-102590509	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs573092297	chr9:102590525-102590526	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs569581433	chr9:102590564-102590565	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs538195489	chr9:102590565-102590566	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs137876606	chr9:102590573-102590574	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs558205063	chr9:102590587-102590588	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs149486371	chr9:102590591-102590592	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs143974118	chr9:102590593-102590594	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs148637005	chr9:102590620-102590621	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs199797073	chr9:102590627-102590628	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs554268298	chr9:102590644-102590645	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs141775492	chr9:102590693-102590694	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs201875863	chr9:102590708-102590709	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs572946695	chr9:102590722-102590723	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs201109859	chr9:102590746-102590747	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs372573982	chr9:102590755-102590756	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs146237875	chr9:102590766-102590767	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs368591388	chr9:102590768-102590769	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs377757850	chr9:102590787-102590788	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs369896512	chr9:102590795-102590796	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs201802808	chr9:102590845-102590846	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs140220595	chr9:102590927-102590928	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs575180948	chr9:102590990-102590991	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs12344570	chr9:102591042-102591043	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs563913405	chr9:102591089-102591090	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs112002668	chr9:102591097-102591098	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs577596679	chr9:102591140-102591141	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs56313530	chr9:102591211-102591212	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs377613134	chr9:102591298-102591299	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs560235039	chr9:102591353-102591354	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs115180962	chr9:102591385-102591386	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs371273879	chr9:102591511-102591512	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs563148441	chr9:102591518-102591519	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs532059256	chr9:102591522-102591523	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Nicotine dependence	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:156 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:102585200-102590200	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
2	chr9:102586800-102609200	Weak transcription	Aorta	Aorta
3	chr9:102587000-102613800	Weak transcription	Hela-S3	cervix
4	chr9:102587200-102590200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr9:102587400-102590200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr9:102587400-102608200	Weak transcription	Psoas Muscle	Psoas
7	chr9:102587600-102590200	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr9:102587600-102590800	Weak transcription	Pancreas	Pancrea
9	chr9:102587800-102590400	Weak transcription	NHLF	lung
10	chr9:102587800-102590800	Bivalent Enhancer	Fetal Brain Male	brain
11	chr9:102588000-102590000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr9:102588200-102590200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr9:102588200-102590400	Weak transcription	Gastric	stomach
14	chr9:102588200-102590400	Weak transcription	Right Ventricle	heart
15	chr9:102588200-102590400	Weak transcription	Spleen	Spleen
16	chr9:102588200-102591400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
17	chr9:102588200-102595400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr9:102589200-102591200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr9:102589200-102592600	Strong transcription	Left Ventricle	heart
20	chr9:102589800-102590000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
21	chr9:102589800-102590000	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
22	chr9:102589800-102590400	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
23	chr9:102589800-102591200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr9:102589800-102592600	Strong transcription	Stomach Smooth Muscle	stomach
25	chr9:102590000-102590200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
26	chr9:102590000-102592600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr9:102590200-102590400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
28	chr9:102590200-102590400	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
29	chr9:102590200-102590600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
30	chr9:102590200-102590600	Genic enhancers	Primary T helper cells PMA-I stimulated	--
31	chr9:102590200-102591400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
32	chr9:102590200-102591400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
33	chr9:102590200-102591400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
34	chr9:102590200-102591400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
35	chr9:102590200-102591600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
36	chr9:102590200-102592200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr9:102590200-102592400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr9:102590200-102592400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr9:102590200-102592600	Strong transcription	Skeletal Muscle Male	skeletal muscle
40	chr9:102590400-102590600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
41	chr9:102590400-102590600	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr9:102590400-102590600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr9:102590400-102590600	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
44	chr9:102590400-102590600	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr9:102590400-102590600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr9:102590400-102590600	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
47	chr9:102590400-102590600	Genic enhancers	Right Ventricle	heart
48	chr9:102590400-102590800	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr9:102590400-102590800	Bivalent Enhancer	Fetal Brain Female	brain
50	chr9:102590400-102590800	Enhancers	Gastric	stomach

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