Variant report

Variant	nsv981589
Chromosome Location	chr7:138163846-138177455
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:77)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:77 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:138168342-138168533	HepG2	liver:	n/a	n/a
2	CEBPB	chr7:138176122-138176217	HepG2	liver:	n/a	chr7:138176172-138176183
3	CEBPB	chr7:138165025-138165139	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr7:138176042-138176294	Hela-S3	cervix:	n/a	chr7:138176172-138176183
5	CTCF	chr7:138167669-138167709	GM10248	blood:	n/a	n/a
6	CTCF	chr7:138171453-138171494	Kidney_OC	kidney:	n/a	n/a
7	CTCF	chr7:138170158-138170255	GM13976	blood:	n/a	n/a
8	EP300	chr7:138166733-138166789	HepG2	liver:	n/a	n/a
9	EP300	chr7:138166750-138166848	K562	blood:	n/a	n/a
10	FOXA1	chr7:138168326-138168691	HepG2	liver:	n/a	n/a
11	FOXA1	chr7:138168218-138168834	HepG2	liver:	n/a	n/a
12	FOXA2	chr7:138168294-138168633	HepG2	liver:	n/a	n/a
13	GATA2	chr7:138176789-138177044	SH-SY5Y	brain:	n/a	n/a
14	GATA3	chr7:138168097-138168280	SH-SY5Y	brain:	n/a	n/a
15	HNF4G	chr7:138168515-138168865	HepG2	liver:	n/a	chr7:138168711-138168726
16	IRF1	chr7:138166512-138166848	K562	blood:	n/a	chr7:138166796-138166806
17	IRF1	chr7:138166479-138166864	K562	blood:	n/a	chr7:138166796-138166806
18	NFYA	chr7:138176522-138176693	GM12878	blood:	n/a	n/a
19	NRF1	chr7:138166769-138166927	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr7:138177396-138177592	HepG2	liver:	n/a	n/a
21	POLR2A	chr7:138164092-138164357	HepG2	liver:	n/a	n/a
22	POLR2A	chr7:138166270-138166581	HepG2	liver:	n/a	n/a
23	POLR2A	chr7:138175711-138176554	HepG2	liver:	n/a	n/a
24	POLR2A	chr7:138164096-138164413	HepG2	liver:	n/a	n/a
25	POLR2A	chr7:138177103-138177375	HepG2	liver:	n/a	n/a
26	POLR2A	chr7:138163186-138164117	HepG2	liver:	n/a	n/a
27	POLR2A	chr7:138169221-138169622	HepG2	liver:	n/a	n/a
28	POLR2A	chr7:138162801-138164379	HepG2	liver:	n/a	n/a
29	POLR2A	chr7:138164138-138164386	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr7:138165357-138165524	HepG2	liver:	n/a	n/a
31	POLR2A	chr7:138166235-138166266	HepG2	liver:	n/a	n/a
32	POLR2A	chr7:138167722-138167770	A549	lung:	n/a	n/a
33	POLR2A	chr7:138177077-138177094	HepG2	liver:	n/a	n/a
34	POLR2A	chr7:138177412-138177600	HepG2	liver:	n/a	n/a
35	POLR2A	chr7:138177037-138177073	HepG2	liver:	n/a	n/a
36	POLR2A	chr7:138168000-138168862	HepG2	liver:	n/a	n/a
37	POLR2A	chr7:138164183-138164264	GM12878	blood:	n/a	n/a
38	POLR2A	chr7:138165005-138165435	HepG2	liver:	n/a	n/a
39	POLR2A	chr7:138165800-138166161	HepG2	liver:	n/a	n/a
40	POLR2A	chr7:138170141-138170410	HepG2	liver:	n/a	n/a
41	POLR2A	chr7:138165875-138168933	HepG2	liver:	n/a	n/a
42	POLR2A	chr7:138177346-138177747	K562	blood:	n/a	n/a
43	POLR2A	chr7:138164220-138164355	A549	lung:	n/a	n/a
44	POLR2A	chr7:138168039-138168715	K562	blood:	n/a	n/a
45	POLR2A	chr7:138165301-138165619	K562	blood:	n/a	n/a
46	POLR2A	chr7:138163796-138164488	HepG2	liver:	n/a	n/a
47	POLR2A	chr7:138166601-138167770	HepG2	liver:	n/a	n/a
48	POLR2A	chr7:138166472-138166490	MCF-7	breast:	n/a	n/a
49	POLR2A	chr7:138164766-138165694	HepG2	liver:	n/a	n/a
50	POLR2A	chr7:138176367-138176518	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:138176808-138176858	PFSK-1	brain:	n/a
2	chr7:138176808-138176858	GM19239	blood:	n/a
3	chr7:138176808-138176858	SK-N-MC	brain:	n/a
4	chr7:138176808-138176858	GM12892	blood:	n/a
5	chr7:138176808-138176858	BJ	skin:	n/a
6	chr7:138176808-138176858	AG10803	skin:	n/a
7	chr7:138176808-138176858	NT2-D1	testis:	n/a
8	chr7:138176808-138176858	HRPEpiC	eye:	n/a
9	chr7:138176808-138176858	Jurkat	blood:	n/a
10	chr7:138176808-138176858	HUVEC	blood vessel:	n/a
11	chr7:138176808-138176858	A549	lung:	n/a
12	chr7:138176808-138176858	Hela-S3	cervix:	n/a
13	chr7:138176808-138176858	LNCaP	prostate:	n/a
14	chr7:138176808-138176858	NHBE	bronchial:	n/a
15	chr7:138176808-138176858	HCT-116	colon:	n/a
16	chr7:138176808-138176858	Caco-2	colon:	n/a
17	chr7:138176808-138176858	HL-60	blood:	n/a
18	chr7:138176808-138176858	HCF	heart:	n/a
19	chr7:138176808-138176858	Hepatocyte	liver:	n/a
20	chr7:138176808-138176858	HNPCEpiC	eye:	n/a
21	chr7:138176808-138176858	HPAEpiC	pulmonary alveolar:	n/a
22	chr7:138176808-138176858	SK-N-SH_RA	brain:	n/a
23	chr7:138176808-138176858	HMEC	breast:	n/a
24	chr7:138176808-138176858	PANC-1	pancreas:	n/a
25	chr7:138176808-138176858	HCM	heart:	n/a
26	chr7:138176808-138176858	IMR90	lung:	fetal
27	chr7:138176808-138176858	NH-A	brain:	n/a
28	chr7:138176808-138176858	AG04449	skin:	fetal
29	chr7:138176808-138176858	HepG2	liver:	n/a
30	chr7:138176808-138176858	AG04450	lung:	fetal
31	chr7:138176808-138176858	RPTEC	kidney:	n/a
32	chr7:138176808-138176858	SK-N-SH	brain:	n/a
33	chr7:138176808-138176858	SAEC	small airway:	n/a
34	chr7:138176808-138176858	HRCEpiC	kidney:	n/a
35	chr7:138176808-138176858	AG09319	gingival:	n/a
36	chr7:138176808-138176858	AG09309	skin:	n/a
37	chr7:138176808-138176858	GM12891	blood:	n/a
38	chr7:138176808-138176858	U87	brain:	n/a
39	chr7:138176808-138176858	AoSMC	blood vessel:	n/a
40	chr7:138176808-138176858	BE2_C	brain:	n/a
41	chr7:138176808-138176858	T-47D	breast:	n/a
42	chr7:138176808-138176858	MCF-7	breast:	n/a
43	chr7:138176808-138176858	GM06990	blood:	n/a
44	chr7:138176808-138176858	HIPEpiC	eye:	n/a
45	chr7:138176808-138176858	ECC-1	luminal epithelium:	n/a
46	chr7:138176808-138176858	HCPEpiC	choroid plexus:	n/a
47	chr7:138176808-138176858	HRE	kidney:	n/a
48	chr7:138176808-138176858	GM12878	blood:	n/a
49	chr7:138176808-138176858	ProgFib	skin:	n/a
50	chr7:138176808-138176858	PrEC	prostate:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:138064132..138065748-chr7:138161608..138163867,2	K562	blood:
2	chr7:138143601..138146619-chr7:138166848..138169714,4	K562	blood:
3	chr7:138156609..138159156-chr7:138163880..138167258,3	K562	blood:
4	chr7:138163657..138165356-chr7:138165416..138167827,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000239123	TF binding region
ENSG00000234995	TF binding region
ENSG00000239123	CpG island
ENSG00000234995	CpG island
ENSG00000239123	chromatin interactions
ENSG00000122779	chromatin interactions

Extended variants
information (count: 510 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:510 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563395647	chr7:138163852-138163853	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs532466172	chr7:138163906-138163907	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs75776820	chr7:138163924-138163925	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs557905506	chr7:138164020-138164021	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs559681676	chr7:138164048-138164049	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs543457358	chr7:138164075-138164076	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs528504006	chr7:138164087-138164088	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs545334031	chr7:138164109-138164110	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs183413701	chr7:138164114-138164115	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs566570769	chr7:138164117-138164118	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs568381499	chr7:138164141-138164142	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs530685712	chr7:138164147-138164148	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs373662799	chr7:138164171-138164172	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs550801164	chr7:138164198-138164199	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs570708470	chr7:138164205-138164206	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs539510277	chr7:138164232-138164233	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs552827394	chr7:138164254-138164255	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs544139539	chr7:138164257-138164258	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs112280060	chr7:138164300-138164301	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs566442779	chr7:138164307-138164308	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs535127903	chr7:138164334-138164335	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs187390272	chr7:138164378-138164379	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs34573655	chr7:138164382-138164383	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs190263893	chr7:138164410-138164411	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs574793443	chr7:138164413-138164414	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs112859747	chr7:138164457-138164458	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs12707387	chr7:138164472-138164473	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs542528008	chr7:138164480-138164481	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs186862801	chr7:138164481-138164482	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs62487616	chr7:138164532-138164533	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs559612048	chr7:138164533-138164534	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs573158624	chr7:138164542-138164543	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs111530832	chr7:138164543-138164544	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs561920469	chr7:138164546-138164547	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs185798887	chr7:138164606-138164607	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs147310873	chr7:138164618-138164619	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs564258086	chr7:138164626-138164627	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs533008461	chr7:138164641-138164642	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs6970145	chr7:138164712-138164713	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs115876002	chr7:138164713-138164714	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs116299942	chr7:138164724-138164725	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs201221166	chr7:138164744-138164745	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs188766827	chr7:138164755-138164756	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs547736338	chr7:138164760-138164761	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs537329890	chr7:138164834-138164835	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs557256916	chr7:138164859-138164860	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs74960805	chr7:138164870-138164871	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs398095418	chr7:138164871-138164872	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs577337990	chr7:138164886-138164887	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs539659373	chr7:138164893-138164894	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Neuroticism	17667963	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute myeloid leukemia	17237825	CNVD
Esophageal cancer	21851588	CNVD
Bladder cancer	21909424	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Low-grade astrocytoma	19016743	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:325 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:138147000-138165000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:138147200-138168400	Weak transcription	Fetal Muscle Leg	muscle
3	chr7:138147200-138183800	Weak transcription	Primary B cells from cord blood	blood
4	chr7:138147200-138189000	Weak transcription	Thymus	Thymus
5	chr7:138148200-138164200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr7:138149800-138188600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr7:138153800-138166200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr7:138153800-138184200	Weak transcription	Fetal Stomach	stomach
9	chr7:138154800-138167200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr7:138155200-138184200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr7:138156000-138165200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr7:138157000-138165200	Enhancers	Liver	Liver
13	chr7:138157600-138164200	Weak transcription	Pancreas	Pancrea
14	chr7:138157600-138191400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr7:138157800-138166800	Weak transcription	Right Atrium	heart
16	chr7:138159400-138165400	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr7:138160200-138175000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr7:138160600-138164200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr7:138160600-138164200	Weak transcription	Lung	lung
20	chr7:138160600-138168400	Weak transcription	Gastric	stomach
21	chr7:138160600-138182200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr7:138161200-138164200	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chr7:138161200-138165400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr7:138161400-138164000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
25	chr7:138161400-138164000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr7:138161400-138164200	Enhancers	Fetal Intestine Large	intestine
27	chr7:138161400-138164400	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr7:138161400-138164400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr7:138161600-138164200	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr7:138161800-138164000	Enhancers	Sigmoid Colon	Sigmoid Colon
31	chr7:138161800-138165000	Enhancers	Stomach Mucosa	stomach
32	chr7:138161800-138165000	Enhancers	HepG2	liver
33	chr7:138161800-138195800	Weak transcription	Fetal Brain Female	brain
34	chr7:138162000-138164000	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr7:138162000-138175200	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr7:138162200-138164000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr7:138162200-138164400	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr7:138162400-138164000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr7:138162400-138165400	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr7:138163000-138164200	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr7:138163000-138164200	Enhancers	Primary T cells from cord blood	blood
42	chr7:138163000-138164400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr7:138163200-138164000	Enhancers	Fetal Heart	heart
44	chr7:138163200-138164200	Enhancers	Primary hematopoietic stem cells	blood
45	chr7:138163200-138164200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr7:138163200-138164200	Enhancers	K562	blood
47	chr7:138163200-138164200	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr7:138163400-138164000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr7:138163400-138164200	Enhancers	H9 Cell Line	embryonic stem cell
50	chr7:138163400-138164200	Enhancers	Fetal Kidney	kidney

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