Variant report

Variant	nsv887821
Chromosome Location	chr7:19381523-19448729
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	ATF3	chr7:19444493-19444867	A549	lung:	n/a	n/a
2	ATF3	chr7:19401699-19402094	HCT-116	colon:	n/a	n/a
3	ATF3	chr7:19444572-19445053	A549	lung:	n/a	n/a
4	BCL3	chr7:19444394-19444990	A549	lung:	n/a	chr7:19444641-19444650
5	BHLHE40	chr7:19437440-19437816	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:19422585-19422633	GM12878	blood:	n/a	n/a
7	CBX3	chr7:19444505-19444941	HCT-116	colon:	n/a	n/a
8	CEBPB	chr7:19406922-19407130	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr7:19444429-19445027	HCT-116	colon:	n/a	n/a
10	CEBPB	chr7:19444511-19445576	Hela-S3	cervix:	n/a	chr7:19445336-19445347
11	CEBPB	chr7:19431952-19432321	IMR90	lung:	n/a	n/a
12	CEBPB	chr7:19401785-19402098	IMR90	lung:	n/a	n/a
13	CEBPB	chr7:19445213-19445455	HepG2	liver:	n/a	chr7:19445336-19445347
14	CEBPB	chr7:19444492-19445539	IMR90	lung:	n/a	chr7:19445336-19445347
15	CEBPB	chr7:19444404-19445628	A549	lung:	n/a	chr7:19445336-19445347
16	CEBPB	chr7:19444478-19444920	A549	lung:	n/a	n/a
17	CEBPB	chr7:19446082-19446303	A549	lung:	n/a	n/a
18	CEBPB	chr7:19445197-19445390	K562	blood:	n/a	chr7:19445336-19445347
19	CEBPB	chr7:19445196-19445500	A549	lung:	n/a	chr7:19445336-19445347
20	CEBPB	chr7:19401780-19402111	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr7:19444604-19444999	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr7:19417480-19417630	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr7:19414707-19414785	ProgFib	skin:	n/a	n/a
24	CTCF	chr7:19424104-19424180	Gliobla	brain:	n/a	n/a
25	CTCF	chr7:19420200-19420350	GM12871	blood:	n/a	n/a
26	CTCF	chr7:19438560-19438710	SK-N-SH_RA	brain:	n/a	n/a
27	CUX1	chr7:19437572-19437772	GM12878	blood:	n/a	n/a
28	E2F4	chr7:19426135-19426335	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr7:19401473-19402035	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr7:19400767-19401001	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr7:19444475-19444985	MCF10A-Er-Src	breast:	n/a	n/a
32	EBF1	chr7:19437513-19437833	GM12878	blood:	n/a	n/a
33	EGR1	chr7:19444335-19444860	HCT-116	colon:	n/a	chr7:19444572-19444583 chr7:19444570-19444585
34	EGR1	chr7:19444360-19444973	HCT-116	colon:	n/a	chr7:19444572-19444583 chr7:19444570-19444585
35	ELK1	chr7:19447125-19447233	GM12878	blood:	n/a	n/a
36	EP300	chr7:19406047-19406052	GM12878	blood:	n/a	n/a
37	EP300	chr7:19444537-19444987	Hela-S3	cervix:	n/a	chr7:19444641-19444650
38	EP300	chr7:19444509-19444813	SK-N-SH_RA	brain:	n/a	chr7:19444641-19444650
39	EP300	chr7:19445189-19445513	Hela-S3	cervix:	n/a	n/a
40	EP300	chr7:19444357-19445176	A549	lung:	n/a	chr7:19444641-19444650
41	EP300	chr7:19444530-19444846	SK-N-SH_RA	brain:	n/a	chr7:19444641-19444650
42	EP300	chr7:19444376-19445548	SK-N-SH	brain:	n/a	chr7:19444641-19444650
43	EP300	chr7:19447044-19447155	GM12878	blood:	n/a	n/a
44	EP300	chr7:19444309-19445094	A549	lung:	n/a	chr7:19444641-19444650
45	FOS	chr7:19392969-19393039	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr7:19431890-19432300	HUVEC	blood vessel:	n/a	chr7:19432104-19432116
47	FOS	chr7:19431984-19432249	MCF10A-Er-Src	breast:	n/a	chr7:19432104-19432116
48	FOS	chr7:19445195-19445524	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr7:19401717-19402113	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr7:19417254-19417376	MCF10A-Er-Src	breast:	n/a	chr7:19417310-19417319 chr7:19417327-19417335 chr7:19417326-19417336 chr7:19417328-19417335 chr7:19417327-19417335 chr7:19417326-19417336 chr7:19417311-19417320 chr7:19417326-19417336 chr7:19417326-19417336 chr7:19417312-19417321 chr7:19417325-19417337

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:19417585-19417635	SK-N-SH_RA	brain:	n/a
2	chr7:19417585-19417635	HRPEpiC	eye:	n/a
3	chr7:19408343-19408393	AG10803	skin:	n/a
4	chr7:19443825-19443875	MCF-7	breast:	n/a
5	chr7:19417585-19417635	PANC-1	pancreas:	n/a
6	chr7:19443825-19443875	Hepatocyte	liver:	n/a
7	chr7:19443825-19443875	A549	lung:	n/a
8	chr7:19443825-19443875	SK-N-SH	brain:	n/a
9	chr7:19443825-19443875	HIPEpiC	eye:	n/a
10	chr7:19408343-19408393	Hepatocyte	liver:	n/a
11	chr7:19443825-19443875	HCF	heart:	n/a
12	chr7:19417585-19417635	GM12892	blood:	n/a
13	chr7:19408343-19408393	PANC-1	pancreas:	n/a
14	chr7:19417585-19417635	ProgFib	skin:	n/a
15	chr7:19417585-19417635	Hepatocyte	liver:	n/a
16	chr7:19417585-19417635	PFSK-1	brain:	n/a
17	chr7:19408343-19408393	HRPEpiC	eye:	n/a
18	chr7:19408343-19408393	HRE	kidney:	n/a
19	chr7:19443825-19443875	HRPEpiC	eye:	n/a
20	chr7:19417585-19417635	MCF-7	breast:	n/a
21	chr7:19443825-19443875	HCPEpiC	choroid plexus:	n/a
22	chr7:19443825-19443875	GM12892	blood:	n/a
23	chr7:19408343-19408393	U87	brain:	n/a
24	chr7:19417585-19417635	K562	blood:	n/a
25	chr7:19408343-19408393	MCF10A-Er-Src	breast:	n/a
26	chr7:19443825-19443875	SK-N-SH_RA	brain:	n/a
27	chr7:19443825-19443875	HCT-116	colon:	n/a
28	chr7:19408343-19408393	AoSMC	blood vessel:	n/a
29	chr7:19417585-19417635	NHBE	bronchial:	n/a
30	chr7:19417585-19417635	A549	lung:	n/a
31	chr7:19408343-19408393	HEK293	kidney:	embryo
32	chr7:19417585-19417635	MCF10A-Er-Src	breast:	n/a
33	chr7:19443825-19443875	HUVEC	blood vessel:	n/a
34	chr7:19417585-19417635	LNCaP	prostate:	n/a
35	chr7:19408343-19408393	HIPEpiC	eye:	n/a
36	chr7:19408343-19408393	HPAEpiC	pulmonary alveolar:	n/a
37	chr7:19443825-19443875	HEEpiC	esophagus:	n/a
38	chr7:19417585-19417635	RPTEC	kidney:	n/a
39	chr7:19417585-19417635	Hela-S3	cervix:	n/a
40	chr7:19408343-19408393	NHDF-neo	bronchial:	n/a
41	chr7:19417585-19417635	GM06990	blood:	n/a
42	chr7:19443825-19443875	BJ	skin:	n/a
43	chr7:19443825-19443875	GM06990	blood:	n/a
44	chr7:19408343-19408393	SAEC	small airway:	n/a
45	chr7:19408343-19408393	HAEpiC	amniotic membrane:	n/a
46	chr7:19417585-19417635	HAEpiC	amniotic membrane:	n/a
47	chr7:19443825-19443875	MCF10A-Er-Src	breast:	n/a
48	chr7:19443825-19443875	NHDF-neo	bronchial:	n/a
49	chr7:19443825-19443875	CMK	blood:	n/a
50	chr7:19443825-19443875	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:19400460..19402875-chr7:19412134..19413923,2	K562	blood:
2	chr7:19400460..19402875-chr7:19412134..19413923,2	K562	blood:
3	chr7:19429082..19431210-chr7:19440295..19442664,2	K562	blood:
4	chr7:19429082..19431210-chr7:19440295..19442664,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HDAC9-5	chr7:19444955-19444993	ENSG00000223838
2	lnc-HDAC9-12	chr7:19411480-19411518	NONHSAT119386
3	lnc-HDAC9-5	chr7:19394363-19394508	ENSG00000223838
4	lnc-HDAC9-5	chr7:19443324-19443386	ENSG00000223838
5	lnc-HDAC9-5	chr7:19393157-19393264	ENSG00000223838
6	lnc-HDAC9-12	chr7:19409849-19409911	NONHSAT119386

Variant related genes	Relation type
ENSG00000223838	TF binding region
ENSG00000223838	CpG island

Extended variants
information (count: 1764 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1764 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs887635	chr7:19388535-19388536	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs202207194	chr7:19388567-19388568	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs561151391	chr7:19388587-19388588	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs531787317	chr7:19388603-19388604	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs111925552	chr7:19388621-19388622	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs112985063	chr7:19389172-19389173	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs564830956	chr7:19389177-19389178	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs147029070	chr7:19389185-19389186	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs79766033	chr7:19389189-19389190	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs548191191	chr7:19389212-19389213	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs79897812	chr7:19389215-19389216	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs185601383	chr7:19389216-19389217	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs552128533	chr7:19389232-19389233	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs547003818	chr7:19391019-19391020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557103554	chr7:19391070-19391071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529798564	chr7:19391073-19391074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535774121	chr7:19391112-19391113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs6461424	chr7:19391129-19391130	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs575468303	chr7:19391158-19391159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs570270828	chr7:19391172-19391173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs201415329	chr7:19391193-19391194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs370401199	chr7:19391195-19391196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs528587643	chr7:19391204-19391205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs74870859	chr7:19391233-19391234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189233317	chr7:19391239-19391240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs139628489	chr7:19391266-19391267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181276650	chr7:19391326-19391327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149707488	chr7:19391334-19391335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538840895	chr7:19391337-19391338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186364908	chr7:19391360-19391361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs543093279	chr7:19391367-19391368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs6955993	chr7:19391368-19391369	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs544138148	chr7:19391369-19391370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs565293577	chr7:19391375-19391376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556327153	chr7:19391398-19391399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577736438	chr7:19391452-19391453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546335838	chr7:19391464-19391465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551268268	chr7:19391476-19391477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs147410793	chr7:19391530-19391531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs528577656	chr7:19391534-19391535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550974668	chr7:19391538-19391539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540680005	chr7:19391562-19391563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10246680	chr7:19391586-19391587	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs535378127	chr7:19391588-19391589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs529590882	chr7:19391597-19391598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558666025	chr7:19391625-19391626	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs569447251	chr7:19391627-19391628	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs549172043	chr7:19391646-19391647	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs533381678	chr7:19391767-19391768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551536916	chr7:19391799-19391800	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:327 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:19391000-19393400	Enhancers	NHDF-Ad	bronchial
2	chr7:19391200-19391800	Enhancers	Dnd41	blood
3	chr7:19391400-19392200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr7:19391600-19392000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr7:19391600-19392800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr7:19391600-19393200	Enhancers	HSMM	muscle
7	chr7:19391600-19393600	Enhancers	Osteobl	bone
8	chr7:19391800-19393200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr7:19391800-19393400	Enhancers	Muscle Satellite Cultured Cells	--
10	chr7:19392000-19393000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr7:19392200-19393400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr7:19393000-19393800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr7:19393400-19394800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr7:19394000-19394400	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr7:19394000-19394800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr7:19401000-19403200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr7:19401600-19402200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr7:19401600-19402400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr7:19401600-19402400	Enhancers	NHDF-Ad	bronchial
20	chr7:19401800-19402200	Enhancers	Muscle Satellite Cultured Cells	--
21	chr7:19401800-19402400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr7:19401800-19402400	Enhancers	Brain Hippocampus Middle	brain
23	chr7:19402000-19402400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr7:19402000-19402600	Enhancers	Brain Cingulate Gyrus	brain
25	chr7:19402000-19402600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr7:19402400-19402800	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr7:19402400-19407600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr7:19402400-19407600	Weak transcription	NHDF-Ad	bronchial
29	chr7:19402600-19406000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr7:19404000-19406000	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr7:19404200-19404400	Enhancers	H9 Cell Line	embryonic stem cell
32	chr7:19404200-19404800	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr7:19404200-19404800	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr7:19404200-19405200	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr7:19404200-19406000	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr7:19404200-19406200	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr7:19404400-19404800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr7:19404400-19405000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr7:19404400-19405000	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr7:19404400-19408200	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr7:19404800-19405200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
42	chr7:19404800-19407800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr7:19404800-19408400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:19405000-19405200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr7:19405000-19408000	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr7:19405200-19406400	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr7:19405200-19408000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr7:19405200-19408400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr7:19406000-19406400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr7:19406000-19408200	Weak transcription	iPS-15b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links