Variant report

Variant	nsv966879
Chromosome Location	chr7:121037613-121041162
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:180)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:180 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:121037989-121038599	HepG2	liver:	n/a	n/a
2	BHLHE40	chr7:121038236-121038664	HepG2	liver:	n/a	n/a
3	BHLHE40	chr7:121037507-121037646	K562	blood:	n/a	n/a
4	BHLHE40	chr7:121038319-121038590	K562	blood:	n/a	n/a
5	CTCF	chr7:121038440-121038590	GM12873	blood:	n/a	n/a
6	CTCF	chr7:121038480-121038630	A549	lung:	n/a	n/a
7	CTCF	chr7:121038500-121038650	SAEC	small airway:	n/a	n/a
8	CTCF	chr7:121038277-121038747	SK-N-SH	brain:	n/a	n/a
9	CTCF	chr7:121038460-121038610	GM12864	blood:	n/a	n/a
10	CTCF	chr7:121038507-121038628	K562	blood:	n/a	n/a
11	CTCF	chr7:121038534-121038663	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr7:121038520-121038670	GM12875	blood:	n/a	n/a
13	CTCF	chr7:121038470-121038687	MCF-7	breast:	n/a	n/a
14	CTCF	chr7:121038411-121038679	A549	lung:	n/a	n/a
15	CTCF	chr7:121038397-121038650	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr7:121038359-121038787	MCF-7	breast:	n/a	n/a
17	CTCF	chr7:121038460-121038610	HepG2	liver:	n/a	n/a
18	CTCF	chr7:121038500-121038650	GM12872	blood:	n/a	n/a
19	CTCF	chr7:121038520-121038670	GM12873	blood:	n/a	n/a
20	CTCF	chr7:121038400-121038550	HFF	foreskin:	n/a	n/a
21	CTCF	chr7:121038525-121038634	GM13976	blood:	n/a	n/a
22	CTCF	chr7:121038520-121038670	RPTEC	kidney:	n/a	n/a
23	CTCF	chr7:121038462-121038648	Pancreas_OC	pancreas:	n/a	n/a
24	CTCF	chr7:121038501-121038648	GM19239	blood:	n/a	n/a
25	CTCF	chr7:121038451-121038687	MCF-7	breast:	n/a	n/a
26	CTCF	chr7:121038518-121038622	GM10266	blood:	n/a	n/a
27	CTCF	chr7:121038480-121038630	HAc	cerebellar:	n/a	n/a
28	CTCF	chr7:121038500-121038650	HMF	breast:	n/a	n/a
29	CTCF	chr7:121038500-121038650	Caco-2	colon:	n/a	n/a
30	CTCF	chr7:121038391-121038727	GM12878	blood:	n/a	n/a
31	CTCF	chr7:121038500-121038650	MCF-7	breast:	n/a	n/a
32	CTCF	chr7:121038520-121038670	AG09319	gingival:	n/a	n/a
33	CTCF	chr7:121038511-121038664	MCF-7	breast:	n/a	n/a
34	CTCF	chr7:121038500-121038650	HRE	kidney:	n/a	n/a
35	CTCF	chr7:121038520-121038670	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr7:121038498-121038680	MCF-7	breast:	n/a	n/a
37	CTCF	chr7:121038420-121038570	GM12867	blood:	n/a	n/a
38	CTCF	chr7:121038520-121038670	HCT-116	colon:	n/a	n/a
39	CTCF	chr7:121038520-121038670	AG04450	lung:	n/a	n/a
40	CTCF	chr7:121038420-121038570	HFF-Myc	foreskin:	n/a	n/a
41	CTCF	chr7:121038648-121038649	GM10248	blood:	n/a	n/a
42	CTCF	chr7:121038480-121038630	HMF	breast:	n/a	n/a
43	CTCF	chr7:121038514-121038643	GM10248	blood:	n/a	n/a
44	CTCF	chr7:121038540-121038690	BE2_C	brain:	n/a	n/a
45	CTCF	chr7:121038500-121038650	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr7:121038540-121038690	HVMF	connective:	n/a	n/a
47	CTCF	chr7:121038539-121038646	GM12891	blood:	n/a	n/a
48	CTCF	chr7:121038485-121038678	A549	lung:	n/a	n/a
49	CTCF	chr7:121038464-121038623	Medullo	brain:	n/a	n/a
50	CTCF	chr7:121038482-121038708	IMR90	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:121040311-121040361	Hela-S3	cervix:	n/a
2	chr7:121040311-121040361	HepG2	liver:	n/a
3	chr7:121040311-121040361	HCPEpiC	choroid plexus:	n/a
4	chr7:121040311-121040361	HNPCEpiC	eye:	n/a
5	chr7:121040311-121040361	NT2-D1	testis:	n/a
6	chr7:121040311-121040361	Jurkat	blood:	n/a
7	chr7:121040311-121040361	SK-N-SH_RA	brain:	n/a
8	chr7:121040311-121040361	PFSK-1	brain:	n/a
9	chr7:121040311-121040361	A549	lung:	n/a
10	chr7:121040311-121040361	GM12878	blood:	n/a
11	chr7:121040311-121040361	HEK293	kidney:	embryo
12	chr7:121040311-121040361	GM06990	blood:	n/a
13	chr7:121040311-121040361	Hepatocyte	liver:	n/a
14	chr7:121040311-121040361	PANC-1	pancreas:	n/a
15	chr7:121040311-121040361	HIPEpiC	eye:	n/a
16	chr7:121040311-121040361	HCF	heart:	n/a
17	chr7:121040311-121040361	HUVEC	blood vessel:	n/a
18	chr7:121040311-121040361	AoSMC	blood vessel:	n/a
19	chr7:121040311-121040361	GM19239	blood:	n/a
20	chr7:121040311-121040361	HCM	heart:	n/a
21	chr7:121040311-121040361	BE2_C	brain:	n/a
22	chr7:121040311-121040361	ovcar-3	ovarian:	n/a
23	chr7:121040311-121040361	BJ	skin:	n/a
24	chr7:121040311-121040361	AG09309	skin:	n/a
25	chr7:121040311-121040361	NHBE	bronchial:	n/a
26	chr7:121040311-121040361	GM12891	blood:	n/a
27	chr7:121040311-121040361	HMEC	breast:	n/a
28	chr7:121040311-121040361	ProgFib	skin:	n/a
29	chr7:121040311-121040361	SK-N-MC	brain:	n/a
30	chr7:121040311-121040361	NH-A	brain:	n/a
31	chr7:121040311-121040361	HPAEpiC	pulmonary alveolar:	n/a
32	chr7:121040311-121040361	K562	blood:	n/a
33	chr7:121040311-121040361	HAEpiC	amniotic membrane:	n/a
34	chr7:121040311-121040361	U87	brain:	n/a
35	chr7:121040311-121040361	SKMC	muscle:	n/a
36	chr7:121040311-121040361	MCF10A-Er-Src	breast:	n/a
37	chr7:121040311-121040361	MCF-7	breast:	n/a
38	chr7:121040311-121040361	GM12892	blood:	n/a
39	chr7:121040311-121040361	PrEC	prostate:	n/a
40	chr7:121040311-121040361	SK-N-SH	brain:	n/a
41	chr7:121040311-121040361	HRE	kidney:	n/a
42	chr7:121040311-121040361	NB4	blood:	n/a
43	chr7:121040311-121040361	NHDF-neo	bronchial:	n/a
44	chr7:121040311-121040361	AG10803	skin:	n/a
45	chr7:121040311-121040361	IMR90	lung:	fetal
46	chr7:121040311-121040361	Caco-2	colon:	n/a
47	chr7:121040311-121040361	LNCaP	prostate:	n/a
48	chr7:121040311-121040361	H1-hESC	embryonic stem cell:	embryo
49	chr7:121040311-121040361	HCT-116	colon:	n/a
50	chr7:121040311-121040361	ECC-1	luminal epithelium:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:121034886..121037643-chr7:121057416..121062764,7	MCF-7	breast:
2	chr7:121040208..121042510-chr7:121052068..121053591,2	K562	blood:
3	chr7:121041056..121042728-chr7:121042964..121044527,2	K562	blood:
4	chr7:121040420..121043103-chr7:121184130..121186484,2	MCF-7	breast:
5	chr7:121034329..121037845-chrX:23092301..23095324,3	K562	blood:
6	chr7:121034674..121038453-chr7:121040021..121045279,6	MCF-7	breast:
7	chr7:121040519..121042218-chr7:121046116..121048635,2	K562	blood:
8	chr7:121035574..121037845-chrX:23093806..23095324,2	K562	blood:
9	chr7:121038659..121042008-chr7:121051096..121053967,4	K562	blood:

No data

Variant related genes	Relation type
CYCSP19	TF binding region
FAM3C	TF binding region
CYCSP19	CpG island
FAM3C	CpG island
ENSG00000174028	chromatin interactions
ENSG00000196937	chromatin interactions
ENSG00000227371	chromatin interactions

Extended variants
information (count: 121 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:121 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553458473	chr7:121037618-121037619	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs73440268	chr7:121037641-121037642	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs569499814	chr7:121037661-121037662	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs2952582	chr7:121037697-121037698	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs548741285	chr7:121037706-121037707	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs71170252	chr7:121037823-121037824	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs568360221	chr7:121037868-121037869	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs534202900	chr7:121037913-121037914	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs552952285	chr7:121038073-121038074	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs572669429	chr7:121038122-121038123	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs13243981	chr7:121038123-121038124	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs2697187	chr7:121038155-121038156	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs369989577	chr7:121038166-121038167	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs575109173	chr7:121038168-121038169	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs372142723	chr7:121038192-121038193	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs150614187	chr7:121038193-121038194	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs574344367	chr7:121038252-121038253	Weak transcription Enhancers Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs376797343	chr7:121038325-121038326	Weak transcription Enhancers Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs556744296	chr7:121038392-121038393	Weak transcription Enhancers Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs76609163	chr7:121038410-121038411	Enhancers Weak transcription Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs368656397	chr7:121038426-121038427	Enhancers Weak transcription Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs546535872	chr7:121038440-121038441	Enhancers Weak transcription Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs191962039	chr7:121038486-121038487	Enhancers Weak transcription Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs149795073	chr7:121038500-121038501	Enhancers Weak transcription Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs55949719	chr7:121038515-121038516	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs144802620	chr7:121038613-121038614	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs55904653	chr7:121038619-121038620	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs568580399	chr7:121038621-121038622	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs116764220	chr7:121038665-121038666	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs139718234	chr7:121038727-121038728	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs184947596	chr7:121038759-121038760	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs190548289	chr7:121038819-121038820	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs538508237	chr7:121038832-121038833	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs558435456	chr7:121038861-121038862	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs117385106	chr7:121038885-121038886	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs537692376	chr7:121038917-121038918	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs554355056	chr7:121038937-121038938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs55816134	chr7:121038954-121038955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs193247492	chr7:121038959-121038960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539975952	chr7:121038970-121038971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs553694633	chr7:121038989-121038990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184450603	chr7:121039034-121039035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546472632	chr7:121039058-121039059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144357409	chr7:121039072-121039073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs576700585	chr7:121039080-121039081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs1819052	chr7:121039100-121039101	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs189385284	chr7:121039133-121039134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs527755375	chr7:121039281-121039282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547588845	chr7:121039314-121039315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs181244285	chr7:121039322-121039323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Autism	22495311	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
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	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
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	21115979	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Barrett''s adenocarcinoma	18663352	CNVD

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:121036600-121037800	Enhancers	Fetal Heart	heart
2	chr7:121036800-121038400	Weak transcription	Pancreas	Pancrea
3	chr7:121036800-121038800	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr7:121036800-121041400	Weak transcription	HSMM	muscle
5	chr7:121036800-121043800	Weak transcription	Ovary	ovary
6	chr7:121037000-121037800	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr7:121037000-121038200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr7:121037000-121038400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr7:121037000-121038400	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr7:121037000-121038600	Enhancers	Stomach Mucosa	stomach
11	chr7:121037000-121038800	Enhancers	Fetal Intestine Large	intestine
12	chr7:121037000-121039000	Enhancers	Fetal Intestine Small	intestine
13	chr7:121037000-121040600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr7:121037000-121041000	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr7:121037000-121041400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:121037000-121041400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr7:121037000-121041600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr7:121037000-121042000	Weak transcription	NHDF-Ad	bronchial
19	chr7:121037000-121042600	Weak transcription	Colon Smooth Muscle	Colon
20	chr7:121037200-121037800	Enhancers	A549	lung
21	chr7:121037200-121038400	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr7:121037200-121038400	Weak transcription	Brain Hippocampus Middle	brain
23	chr7:121037400-121038000	Flanking Active TSS	HepG2	liver
24	chr7:121037400-121038400	Weak transcription	Duodenum Mucosa	Duodenum
25	chr7:121037600-121037800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr7:121037600-121038000	Enhancers	Liver	Liver
27	chr7:121037600-121038200	Weak transcription	Fetal Kidney	kidney
28	chr7:121037800-121038400	Active TSS	Rectal Mucosa Donor 29	rectum
29	chr7:121037800-121038600	Active TSS	Pancreatic Islets	Pancreatic Islet
30	chr7:121038000-121038600	Active TSS	Liver	Liver
31	chr7:121038000-121038600	Active TSS	HepG2	liver
32	chr7:121038200-121038800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr7:121038200-121038800	Enhancers	Fetal Kidney	kidney
34	chr7:121038400-121038600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr7:121038400-121038600	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr7:121038400-121038600	Enhancers	Brain Substantia Nigra	brain
37	chr7:121038400-121038800	Enhancers	Duodenum Mucosa	Duodenum
38	chr7:121038400-121038800	Enhancers	Pancreas	Pancrea
39	chr7:121038600-121038800	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr7:121038600-121038800	Enhancers	Brain Hippocampus Middle	brain
41	chr7:121038600-121039000	Enhancers	Liver	Liver
42	chr7:121040400-121041600	Weak transcription	Osteobl	bone
43	chr7:121040600-121043400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr7:121041000-121043000	Enhancers	Muscle Satellite Cultured Cells	--

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