Variant report

Variant	nsv615644
Chromosome Location	chr9:136527226-136534391
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	CTBP2	chr9:136534359-136535043	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr9:136529911-136530055	NHEK	skin:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
3	CTCF	chr9:136529920-136530070	GM12871	blood:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
4	CTCF	chr9:136529755-136530185	MCF-7	breast:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
5	CTCF	chr9:136529880-136530030	HVMF	connective:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
6	CTCF	chr9:136529877-136530077	GM12891	blood:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
7	CTCF	chr9:136529881-136530076	GM19240	blood:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
8	CTCF	chr9:136529860-136530010	AG09319	gingival:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
9	CTCF	chr9:136529880-136530081	GM12892	blood:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
10	CTCF	chr9:136529872-136530089	MCF-7	breast:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
11	CTCF	chr9:136529920-136530070	HA-sp	spinal cord:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
12	CTCF	chr9:136529940-136530090	GM12872	blood:	n/a	chr9:136529963-136529976
13	CTCF	chr9:136529940-136530090	HCT-116	colon:	n/a	chr9:136529963-136529976
14	CTCF	chr9:136529931-136530026	A549	lung:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
15	CTCF	chr9:136529900-136530050	WERI-Rb-1	eye:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
16	CTCF	chr9:136529920-136530070	MCF-7	breast:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
17	CTCF	chr9:136529888-136530053	GM19238	blood:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
18	CTCF	chr9:136529959-136530025	Lung_OC	lung:	n/a	chr9:136529963-136529976
19	CTCF	chr9:136529860-136530010	MCF-7	breast:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
20	CTCF	chr9:136531216-136531309	H1-hESC	embryonic stem cell:	n/a	chr9:136531248-136531261
21	CTCF	chr9:136529880-136530030	HBMEC	blood vessel:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
22	CTCF	chr9:136529860-136530010	HEK293	kidney:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
23	CTCF	chr9:136529820-136529970	HRPEpiC	eye:	n/a	chr9:136529939-136529947
24	CTCF	chr9:136529983-136529984	GM12878	blood:	n/a	n/a
25	CTCF	chr9:136529860-136530010	RPTEC	kidney:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
26	CTCF	chr9:136529900-136530050	GM06990	blood:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
27	CTCF	chr9:136529834-136530032	HepG2	liver:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
28	CTCF	chr9:136529882-136530092	MCF-7	breast:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
29	CTCF	chr9:136529880-136530030	HEK293	kidney:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
30	CTCF	chr9:136529920-136530070	SAEC	small airway:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
31	CTCF	chr9:136529945-136529976	HUVEC	blood vessel:	n/a	chr9:136529963-136529976
32	CTCF	chr9:136529900-136530050	HBMEC	blood vessel:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
33	CTCF	chr9:136529860-136530010	AG09309	skin:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
34	CTCF	chr9:136529900-136530050	Hela-S3	cervix:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
35	CTCF	chr9:136529881-136530027	GM12878	blood:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
36	CTCF	chr9:136529900-136530050	Caco-2	colon:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
37	CTCF	chr9:136529894-136530071	Gliobla	brain:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
38	CTCF	chr9:136529863-136530100	MCF-7	breast:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
39	CTCF	chr9:136529889-136530006	SK-N-SH_RA	brain:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
40	CTCF	chr9:136529900-136530050	HCPEpiC	choroid plexus:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
41	CTCF	chr9:136529899-136530058	GM10248	blood:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
42	CTCF	chr9:136529840-136530130	GM12866	blood:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
43	CTCF	chr9:136529954-136530070	GM10266	blood:	n/a	chr9:136529963-136529976
44	CTCF	chr9:136529900-136530050	HepG2	liver:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
45	CTCF	chr9:136529880-136530030	HRPEpiC	eye:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
46	CTCF	chr9:136529820-136529970	HUVEC	blood vessel:	n/a	chr9:136529939-136529947
47	CTCF	chr9:136529880-136530030	BE2_C	brain:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
48	CTCF	chr9:136529902-136530040	Hela-S3	cervix:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
49	CTCF	chr9:136529872-136530099	MCF-7	breast:	n/a	chr9:136529963-136529976 chr9:136529939-136529947
50	CTCF	chr9:136529891-136529925	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:136523144..136526065-chr9:136527921..136530216,2	MCF-7	breast:
2	chr9:136533491..136538951-chr9:136540367..136544630,5	MCF-7	breast:
3	chr9:136528562..136531390-chr9:136533335..136537164,3	K562	blood:
4	chr9:136528592..136530737-chr9:136533318..136534835,2	K562	blood:
5	chr9:136397976..136398826-chr9:136528405..136529390,2	MCF-7	breast:
6	chr9:136528592..136530737-chr9:136533318..136534835,2	K562	blood:
7	chr9:136524956..136527895-chr9:136529322..136531931,3	MCF-7	breast:
8	chr9:136528532..136530062-chr9:136535645..136537164,2	K562	blood:
9	chr9:136528562..136531390-chr9:136533335..136537164,3	K562	blood:
10	chr9:136524956..136527895-chr9:136529322..136531931,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM163B-2	chr9:136531857-136532245	NONHSAT135335
2	lnc-FAM163B-2	chr9:136529094-136529136	NONHSAT135335

Variant related genes	Relation type
DBH-AS1	TF binding region
SARDH	TF binding region

Extended variants
information (count: 409 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:409 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs129885	chr9:136527226-136527227	Genic enhancers Bivalent Enhancer Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182988709	chr9:136527248-136527249	Genic enhancers Bivalent Enhancer Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs544351551	chr9:136527264-136527265	Genic enhancers Bivalent Enhancer Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs368548531	chr9:136527295-136527296	Genic enhancers Bivalent Enhancer Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs556267309	chr9:136527308-136527309	Genic enhancers Bivalent Enhancer Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs536415229	chr9:136527315-136527316	Genic enhancers Bivalent Enhancer Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs3025437	chr9:136527318-136527319	Genic enhancers Bivalent Enhancer Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs3025438	chr9:136527344-136527345	Genic enhancers Bivalent Enhancer Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs560844935	chr9:136527345-136527346	Genic enhancers Bivalent Enhancer Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs572699418	chr9:136527349-136527350	Genic enhancers Bivalent Enhancer Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs187459822	chr9:136527350-136527351	Genic enhancers Bivalent Enhancer Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs564372346	chr9:136527390-136527391	Genic enhancers Bivalent Enhancer Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs372102347	chr9:136527396-136527397	Genic enhancers Bivalent Enhancer Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs3025439	chr9:136527417-136527418	Genic enhancers Weak transcription Bivalent Enhancer Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs549882373	chr9:136527432-136527433	Genic enhancers Weak transcription Bivalent Enhancer Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs561811395	chr9:136527462-136527463	Genic enhancers Weak transcription Bivalent Enhancer Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529259802	chr9:136527469-136527470	Genic enhancers Weak transcription Bivalent Enhancer Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35843704	chr9:136527510-136527511	Genic enhancers Weak transcription Bivalent Enhancer Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs547425754	chr9:136527580-136527581	Genic enhancers Weak transcription Bivalent Enhancer Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs3025440	chr9:136527604-136527605	Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs207470636	chr9:136527617-136527618	Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs150024007	chr9:136527634-136527635	Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs370785921	chr9:136527635-136527636	Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs3025441	chr9:136527661-136527662	Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs572459700	chr9:136527672-136527673	Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs528663420	chr9:136527734-136527735	Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552427557	chr9:136527754-136527755	Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs145412726	chr9:136527774-136527775	Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs373883703	chr9:136527790-136527791	Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556306053	chr9:136527843-136527844	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574540409	chr9:136527868-136527869	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs535534197	chr9:136527870-136527871	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541165544	chr9:136527875-136527876	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553529181	chr9:136527900-136527901	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571989043	chr9:136527954-136527955	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191447761	chr9:136527978-136527979	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564408575	chr9:136527981-136527982	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576242016	chr9:136527982-136527983	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543569111	chr9:136528003-136528004	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs561848129	chr9:136528004-136528005	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377368713	chr9:136528029-136528030	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577651396	chr9:136528046-136528047	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543430009	chr9:136528050-136528051	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559517419	chr9:136528061-136528062	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533331563	chr9:136528065-136528066	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552516532	chr9:136528118-136528119	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370672110	chr9:136528124-136528125	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538045034	chr9:136528146-136528147	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149209275	chr9:136528149-136528150	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34763434	chr9:136528159-136528160	Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Melanoma	18172304	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Kleefstra Syndrome	21538692	CNVD
Disorders of sex development	22290220	CNVD
Cancer	21183584	CNVD
Chronic myelomonocytic leukemia	16760666	CNVD
Abnormal phenotypes	18644119	CNVD
Ovarian cancer	21720365	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21364760	CNVD
Cancer	20581869	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Hepatocellular carcinoma	22174799	CNVD
Bladder cancer	21909424	CNVD
Cancer	17160897	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20932292	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:136524400-136527800	Weak transcription	Ovary	ovary
2	chr9:136524400-136541200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr9:136524600-136528800	Weak transcription	Spleen	Spleen
4	chr9:136524600-136530800	Weak transcription	Lung	lung
5	chr9:136524800-136535600	Weak transcription	HepG2	liver
6	chr9:136524800-136537000	Weak transcription	Fetal Lung	lung
7	chr9:136524800-136542800	Weak transcription	Right Atrium	heart
8	chr9:136524800-136555600	Weak transcription	HSMM	muscle
9	chr9:136525000-136527800	Weak transcription	Pancreas	Pancrea
10	chr9:136525000-136530800	Weak transcription	Brain Germinal Matrix	brain
11	chr9:136525000-136556800	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr9:136525200-136527800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr9:136525200-136531000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr9:136525200-136534000	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr9:136525200-136534600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr9:136525400-136528600	Weak transcription	Primary T cells from cord blood	blood
17	chr9:136525400-136534600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr9:136525800-136536200	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr9:136526000-136534400	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr9:136526000-136534800	Weak transcription	Fetal Intestine Small	intestine
21	chr9:136526200-136529800	Weak transcription	Thymus	Thymus
22	chr9:136526600-136527400	Weak transcription	Liver	Liver
23	chr9:136527000-136528000	Enhancers	Fetal Thymus	thymus
24	chr9:136527000-136528200	Enhancers	Fetal Muscle Leg	muscle
25	chr9:136527000-136528400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
26	chr9:136527000-136529800	Strong transcription	Fetal Stomach	stomach
27	chr9:136527200-136527400	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr9:136527200-136527400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr9:136527200-136528200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr9:136527400-136527600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr9:136527400-136527600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
32	chr9:136527400-136527800	Strong transcription	Liver	Liver
33	chr9:136527800-136528200	Enhancers	Pancreas	Pancrea
34	chr9:136527800-136528600	Strong transcription	Ovary	ovary
35	chr9:136527800-136529000	Genic enhancers	Liver	Liver
36	chr9:136528000-136528200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
37	chr9:136528000-136528800	Weak transcription	Fetal Thymus	thymus
38	chr9:136528000-136529000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
39	chr9:136528200-136529000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr9:136528200-136529000	Weak transcription	Pancreas	Pancrea
41	chr9:136528200-136529200	Weak transcription	Fetal Muscle Leg	muscle
42	chr9:136528400-136528800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr9:136528400-136540800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr9:136528600-136530800	Strong transcription	Primary T cells from cord blood	blood
45	chr9:136528600-136544200	Weak transcription	Ovary	ovary
46	chr9:136528800-136529400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr9:136528800-136530400	Enhancers	Spleen	Spleen
48	chr9:136528800-136530600	Enhancers	Fetal Thymus	thymus
49	chr9:136529000-136529400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr9:136529000-136529400	Strong transcription	Pancreas	Pancrea

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