Variant report

Variant	nsv892698
Chromosome Location	chr9:18830444-18905289
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	BATF	chr9:18890372-18890733	GM12878	blood:	n/a	chr9:18890552-18890563
2	BATF	chr9:18834825-18835133	GM12878	blood:	n/a	n/a
3	BATF	chr9:18890434-18890714	GM12878	blood:	n/a	chr9:18890552-18890563
4	BATF	chr9:18834786-18835105	GM12878	blood:	n/a	n/a
5	BCL3	chr9:18887844-18888106	GM12878	blood:	n/a	n/a
6	BCL3	chr9:18887784-18888212	GM12878	blood:	n/a	n/a
7	BHLHE40	chr9:18834809-18835097	GM12878	blood:	n/a	n/a
8	BHLHE40	chr9:18847612-18847839	HepG2	liver:	n/a	n/a
9	CEBPB	chr9:18857887-18858057	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr9:18896552-18896779	K562	blood:	n/a	chr9:18896668-18896679
11	CEBPB	chr9:18895575-18895907	HepG2	liver:	n/a	chr9:18895741-18895752
12	CEBPB	chr9:18857976-18858073	A549	lung:	n/a	n/a
13	CEBPB	chr9:18896530-18896830	A549	lung:	n/a	chr9:18896668-18896679
14	CEBPB	chr9:18896500-18896851	HepG2	liver:	n/a	chr9:18896668-18896679
15	CEBPB	chr9:18895594-18895916	IMR90	lung:	n/a	chr9:18895741-18895752
16	CEBPB	chr9:18857833-18858300	IMR90	lung:	n/a	n/a
17	CEBPB	chr9:18859391-18859475	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr9:18896508-18896835	IMR90	lung:	n/a	chr9:18896668-18896679
19	CEBPB	chr9:18868802-18868991	HepG2	liver:	n/a	n/a
20	CEBPB	chr9:18890460-18890693	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr9:18896572-18896814	Hela-S3	cervix:	n/a	chr9:18896668-18896679
22	CTCF	chr9:18863000-18863150	HEK293	kidney:	n/a	chr9:18863040-18863058
23	CTCF	chr9:18862880-18863030	GM12865	blood:	n/a	n/a
24	CTCF	chr9:18863036-18863078	Kidney_OC	kidney:	n/a	chr9:18863040-18863058
25	CTCF	chr9:18861980-18862130	HCM	heart:	n/a	chr9:18862062-18862075
26	CTCF	chr9:18861960-18862110	AoAF	blood vessel:	n/a	chr9:18862062-18862075
27	CTCF	chr9:18863000-18863150	HA-sp	spinal cord:	n/a	chr9:18863040-18863058
28	CTCF	chr9:18861960-18862110	HRPEpiC	eye:	n/a	chr9:18862062-18862075
29	CTCF	chr9:18862940-18863090	NB4	blood:	n/a	chr9:18863040-18863058
30	CTCF	chr9:18862000-18862150	AG09319	gingival:	n/a	chr9:18862062-18862075
31	CTCF	chr9:18862980-18863130	BE2_C	brain:	n/a	chr9:18863040-18863058
32	CTCF	chr9:18862020-18862170	AG04450	lung:	n/a	chr9:18862062-18862075
33	CTCF	chr9:18865840-18865990	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr9:18863031-18863111	GM12878	blood:	n/a	chr9:18863040-18863058
35	CTCF	chr9:18862940-18863090	AG04450	lung:	n/a	chr9:18863040-18863058
36	CTCF	chr9:18866257-18866344	LNCaP	prostate:	n/a	n/a
37	CTCF	chr9:18862940-18863090	HRPEpiC	eye:	n/a	chr9:18863040-18863058
38	CTCF	chr9:18863014-18863144	ProgFib	skin:	n/a	chr9:18863040-18863058
39	CTCF	chr9:18862980-18863130	HPF	lung:	n/a	chr9:18863040-18863058
40	CTCF	chr9:18862920-18863070	HepG2	liver:	n/a	chr9:18863040-18863058
41	CTCF	chr9:18862020-18862170	HPF	lung:	n/a	chr9:18862062-18862075
42	CTCF	chr9:18889300-18889450	AG04449	skin:	n/a	n/a
43	CTCF	chr9:18866311-18866319	LNCaP	prostate:	n/a	n/a
44	CTCF	chr9:18850280-18850430	SK-N-SH_RA	brain:	n/a	chr9:18850386-18850407 chr9:18850392-18850408 chr9:18850391-18850409
45	CTCF	chr9:18863002-18863102	MCF-7	breast:	n/a	chr9:18863040-18863058
46	CTCF	chr9:18862023-18862118	H1-hESC	embryonic stem cell:	n/a	chr9:18862062-18862075
47	CTCF	chr9:18861903-18862196	IMR90	lung:	n/a	chr9:18862062-18862075
48	CTCF	chr9:18862080-18862230	HAc	cerebellar:	n/a	n/a
49	CTCF	chr9:18862840-18862990	GM06990	blood:	n/a	n/a
50	CTCF	chr9:18863060-18863210	HVMF	connective:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:18862115-18862165	PFSK-1	brain:	n/a
2	chr9:18862115-18862165	HPAEpiC	pulmonary alveolar:	n/a
3	chr9:18862115-18862165	HEEpiC	esophagus:	n/a
4	chr9:18862115-18862165	HUVEC	blood vessel:	n/a
5	chr9:18862115-18862165	GM12891	blood:	n/a
6	chr9:18862115-18862165	A549	lung:	n/a
7	chr9:18862115-18862165	SK-N-MC	brain:	n/a
8	chr9:18862115-18862165	HMEC	breast:	n/a
9	chr9:18862115-18862165	NB4	blood:	n/a
10	chr9:18862115-18862165	K562	blood:	n/a
11	chr9:18862115-18862165	AG09319	gingival:	n/a
12	chr9:18862115-18862165	MCF10A-Er-Src	breast:	n/a
13	chr9:18862115-18862165	AG04450	lung:	fetal
14	chr9:18862115-18862165	NHBE	bronchial:	n/a
15	chr9:18862115-18862165	HRPEpiC	eye:	n/a
16	chr9:18862115-18862165	SKMC	muscle:	n/a
17	chr9:18862115-18862165	T-47D	breast:	n/a
18	chr9:18862115-18862165	HNPCEpiC	eye:	n/a
19	chr9:18862115-18862165	ProgFib	skin:	n/a
20	chr9:18862115-18862165	HCPEpiC	choroid plexus:	n/a
21	chr9:18862115-18862165	BJ	skin:	n/a
22	chr9:18862115-18862165	HepG2	liver:	n/a
23	chr9:18862115-18862165	H1-hESC	embryonic stem cell:	embryo
24	chr9:18862115-18862165	AG04449	skin:	fetal
25	chr9:18862115-18862165	LNCaP	prostate:	n/a
26	chr9:18862115-18862165	AG10803	skin:	n/a
27	chr9:18862115-18862165	HCF	heart:	n/a
28	chr9:18862115-18862165	Caco-2	colon:	n/a
29	chr9:18862115-18862165	AoSMC	blood vessel:	n/a
30	chr9:18862115-18862165	GM12892	blood:	n/a
31	chr9:18862115-18862165	HRCEpiC	kidney:	n/a
32	chr9:18862115-18862165	GM19239	blood:	n/a
33	chr9:18862115-18862165	Jurkat	blood:	n/a
34	chr9:18862115-18862165	NH-A	brain:	n/a
35	chr9:18862115-18862165	HRE	kidney:	n/a
36	chr9:18862115-18862165	HIPEpiC	eye:	n/a
37	chr9:18862115-18862165	HCM	heart:	n/a
38	chr9:18862115-18862165	NHDF-neo	bronchial:	n/a
39	chr9:18862115-18862165	SAEC	small airway:	n/a
40	chr9:18862115-18862165	GM12878	blood:	n/a
41	chr9:18862115-18862165	Hepatocyte	liver:	n/a
42	chr9:18862115-18862165	HEK293	kidney:	embryo
43	chr9:18862115-18862165	PrEC	prostate:	n/a
44	chr9:18862115-18862165	HAEpiC	amniotic membrane:	n/a
45	chr9:18862115-18862165	NT2-D1	testis:	n/a
46	chr9:18862115-18862165	GM06990	blood:	n/a
47	chr9:18862115-18862165	AG09309	skin:	n/a
48	chr9:18862115-18862165	BE2_C	brain:	n/a
49	chr9:18862115-18862165	HCT-116	colon:	n/a
50	chr9:18862115-18862165	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:18826203..18828034-chr9:18832223..18834749,2	MCF-7	breast:
2	chr17:59322960..59323509-chr9:18863651..18864333,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000223211	TF binding region
ADAMTSL1	TF binding region
ENSG00000223211	CpG island
ADAMTSL1	CpG island

Extended variants
information (count: 3631 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3631 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16937127	chr9:18830444-18830445	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs544164376	chr9:18830520-18830521	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562562220	chr9:18830527-18830528	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs117261958	chr9:18830533-18830534	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551836179	chr9:18830548-18830549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375311383	chr9:18830595-18830596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs16937129	chr9:18830618-18830619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541198729	chr9:18830624-18830625	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561115078	chr9:18830632-18830633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572339716	chr9:18830657-18830658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs538155928	chr9:18830674-18830675	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs549775631	chr9:18830682-18830683	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571241833	chr9:18830691-18830692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs77262631	chr9:18830728-18830729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138240416	chr9:18830730-18830731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369871305	chr9:18830731-18830732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536785472	chr9:18830762-18830763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553170575	chr9:18830772-18830773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555077220	chr9:18830785-18830786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs572094942	chr9:18830790-18830791	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534357851	chr9:18830798-18830799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576574258	chr9:18830814-18830815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544044160	chr9:18830881-18830882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs111635403	chr9:18830886-18830887	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555553769	chr9:18830890-18830891	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573965381	chr9:18830931-18830932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs142252763	chr9:18830955-18830956	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs35827024	chr9:18831004-18831005	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562875104	chr9:18831006-18831007	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373026623	chr9:18831009-18831010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs578024640	chr9:18831012-18831013	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7858256	chr9:18831022-18831023	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs376839607	chr9:18831030-18831031	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560585882	chr9:18831079-18831080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146023002	chr9:18831091-18831092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542810695	chr9:18831155-18831156	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561088901	chr9:18831173-18831174	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531564749	chr9:18831186-18831187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35629493	chr9:18831188-18831189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369415686	chr9:18831207-18831208	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550085622	chr9:18831326-18831327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7858859	chr9:18831340-18831341	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs7858656	chr9:18831365-18831366	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs183923309	chr9:18831369-18831370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs16937134	chr9:18831423-18831424	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs7859001	chr9:18831444-18831445	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs16937136	chr9:18831482-18831483	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs374895271	chr9:18831500-18831501	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567502289	chr9:18831549-18831550	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76030825	chr9:18831562-18831563	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Myelofibrosis	22110671	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:653 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18818000-18845200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:18823000-18834400	Weak transcription	Rectal Smooth Muscle	rectum
3	chr9:18825400-18833000	Strong transcription	HSMM	muscle
4	chr9:18825400-18833400	Weak transcription	Right Ventricle	heart
5	chr9:18825400-18845200	Weak transcription	HSMMtube	muscle
6	chr9:18825400-18857200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr9:18825600-18833600	Strong transcription	NHDF-Ad	bronchial
8	chr9:18825600-18857400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr9:18826000-18832600	Strong transcription	Muscle Satellite Cultured Cells	--
10	chr9:18826200-18833600	Weak transcription	HUVEC	blood vessel
11	chr9:18826800-18830600	Weak transcription	Gastric	stomach
12	chr9:18826800-18834600	Weak transcription	Fetal Heart	heart
13	chr9:18827200-18861600	Weak transcription	Fetal Muscle Trunk	muscle
14	chr9:18829000-18832400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr9:18829600-18832400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr9:18829800-18830800	Strong transcription	Aorta	Aorta
17	chr9:18830000-18833600	Strong transcription	Osteobl	bone
18	chr9:18830200-18830800	Strong transcription	NHLF	lung
19	chr9:18830200-18845400	Weak transcription	Fetal Muscle Leg	muscle
20	chr9:18830400-18833000	Strong transcription	NH-A	brain
21	chr9:18830400-18833200	Strong transcription	Fetal Stomach	stomach
22	chr9:18830400-18835600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr9:18830800-18845200	Weak transcription	Aorta	Aorta
24	chr9:18830800-18857400	Weak transcription	NHLF	lung
25	chr9:18831600-18832200	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr9:18832400-18837600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr9:18832400-18837800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr9:18832600-18837800	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr9:18833000-18834600	Weak transcription	HSMM	muscle
30	chr9:18833000-18847000	Weak transcription	NH-A	brain
31	chr9:18833200-18845200	Weak transcription	Fetal Stomach	stomach
32	chr9:18833600-18845200	Weak transcription	Osteobl	bone
33	chr9:18833600-18848400	Weak transcription	NHDF-Ad	bronchial
34	chr9:18834600-18835400	Enhancers	GM12878-XiMat	blood
35	chr9:18834600-18835800	Strong transcription	HSMM	muscle
36	chr9:18835600-18835800	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr9:18835800-18837200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr9:18835800-18837400	Weak transcription	HSMM	muscle
39	chr9:18837200-18838800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr9:18837400-18838200	Strong transcription	HSMM	muscle
41	chr9:18837600-18839000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr9:18837800-18838200	Enhancers	Primary T cells from cord blood	blood
43	chr9:18837800-18838800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr9:18837800-18839000	Strong transcription	Muscle Satellite Cultured Cells	--
45	chr9:18838200-18845200	Weak transcription	HSMM	muscle
46	chr9:18838800-18845200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr9:18838800-18849200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr9:18839000-18845200	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr9:18839000-18845200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr9:18845200-18845400	ZNF genes & repeats	Fetal Stomach	stomach

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