Variant report

Variant	esv3362121
Chromosome Location	chr7:4817576-4820124
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:11)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:11 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAFK	chr7:4818007-4818073	HepG2	liver:	n/a	n/a
2	POLR2A	chr7:4819968-4820099	H1-hESC	embryonic stem cell:	n/a	n/a
3	POLR2A	chr7:4817434-4818240	K562	blood:	n/a	n/a
4	POLR2A	chr7:4817650-4818268	GM12878	blood:	n/a	n/a
5	POLR2A	chr7:4817415-4817676	GM12878	blood:	n/a	n/a
6	POLR2A	chr7:4819958-4820087	H1-hESC	embryonic stem cell:	n/a	n/a
7	POLR2A	chr7:4817861-4818236	HepG2	liver:	n/a	n/a
8	POLR2A	chr7:4814016-4818332	IMR90	lung:	n/a	n/a
9	POLR2A	chr7:4818011-4818112	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr7:4817668-4817962	GM12891	blood:	n/a	n/a
11	POLR2A	chr7:4818054-4818252	HUVEC	blood vessel:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4817726-4817776	CMK	blood:	n/a
2	chr7:4817726-4817776	NHBE	bronchial:	n/a
3	chr7:4817726-4817776	HCF	heart:	n/a
4	chr7:4817726-4817776	HRPEpiC	eye:	n/a
5	chr7:4817726-4817776	HL-60	blood:	n/a
6	chr7:4817726-4817776	NT2-D1	testis:	n/a
7	chr7:4817726-4817776	NH-A	brain:	n/a
8	chr7:4817726-4817776	SAEC	small airway:	n/a
9	chr7:4817726-4817776	ProgFib	skin:	n/a
10	chr7:4817726-4817776	HRCEpiC	kidney:	n/a
11	chr7:4817726-4817776	Jurkat	blood:	n/a
12	chr7:4817726-4817776	HMEC	breast:	n/a
13	chr7:4817726-4817776	SK-N-SH_RA	brain:	n/a
14	chr7:4817726-4817776	K562	blood:	n/a
15	chr7:4817726-4817776	BE2_C	brain:	n/a
16	chr7:4817726-4817776	RPTEC	kidney:	n/a
17	chr7:4817726-4817776	HAEpiC	amniotic membrane:	n/a
18	chr7:4817726-4817776	GM06990	blood:	n/a
19	chr7:4817726-4817776	Caco-2	colon:	n/a
20	chr7:4817726-4817776	LNCaP	prostate:	n/a
21	chr7:4817726-4817776	MCF10A-Er-Src	breast:	n/a
22	chr7:4817726-4817776	PANC-1	pancreas:	n/a
23	chr7:4817726-4817776	AG04449	skin:	fetal
24	chr7:4817726-4817776	PrEC	prostate:	n/a
25	chr7:4817726-4817776	HPAEpiC	pulmonary alveolar:	n/a
26	chr7:4817726-4817776	U87	brain:	n/a
27	chr7:4817726-4817776	MCF-7	breast:	n/a
28	chr7:4817726-4817776	AG09319	gingival:	n/a
29	chr7:4817726-4817776	HNPCEpiC	eye:	n/a
30	chr7:4817726-4817776	HCM	heart:	n/a
31	chr7:4817726-4817776	HCT-116	colon:	n/a
32	chr7:4817726-4817776	GM12892	blood:	n/a
33	chr7:4817726-4817776	AG09309	skin:	n/a
34	chr7:4817726-4817776	Hela-S3	cervix:	n/a
35	chr7:4817726-4817776	AoSMC	blood vessel:	n/a
36	chr7:4817726-4817776	PFSK-1	brain:	n/a
37	chr7:4817726-4817776	HepG2	liver:	n/a
38	chr7:4817726-4817776	A549	lung:	n/a
39	chr7:4817726-4817776	GM12891	blood:	n/a
40	chr7:4817726-4817776	IMR90	lung:	fetal
41	chr7:4817726-4817776	AG10803	skin:	n/a
42	chr7:4817726-4817776	NB4	blood:	n/a
43	chr7:4817726-4817776	ECC-1	luminal epithelium:	n/a
44	chr7:4817726-4817776	HEK293	kidney:	embryo
45	chr7:4817726-4817776	ovcar-3	ovarian:	n/a
46	chr7:4817726-4817776	HIPEpiC	eye:	n/a
47	chr7:4817726-4817776	HEEpiC	esophagus:	n/a
48	chr7:4817726-4817776	GM19239	blood:	n/a
49	chr7:4817726-4817776	SK-N-SH	brain:	n/a
50	chr7:4817726-4817776	HRE	kidney:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:4815353..4817520-chr7:4819712..4821919,3	K562	blood:
2	chr7:4813279..4817996-chr7:4818432..4827499,15	MCF-7	breast:
3	chr7:4815181..4818417-chr7:4818963..4822652,6	K562	blood:
4	chr7:4803747..4806445-chr7:4817693..4820028,2	K562	blood:
5	chr7:4813279..4817996-chr7:4818432..4827499,15	MCF-7	breast:
6	chr7:4813801..4815751-chr7:4816573..4818278,2	MCF-7	breast:
7	chr7:4818366..4820585-chr7:4824717..4826372,2	K562	blood:

No data

Variant related genes	Relation type
AP5Z1	TF binding region
AP5Z1	CpG island
ENSG00000242802	chromatin interactions

Extended variants
information (count: 134 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:134 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535152143	chr7:4817588-4817589	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs553821216	chr7:4817599-4817600	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs572179835	chr7:4817616-4817617	Weak transcription Genic enhancers Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs544493750	chr7:4817645-4817646	Weak transcription Genic enhancers Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs10278732	chr7:4817648-4817649	Weak transcription Genic enhancers Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs545995034	chr7:4817670-4817671	Weak transcription Genic enhancers Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs189672561	chr7:4817678-4817679	Weak transcription Genic enhancers Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs576340368	chr7:4817713-4817714	Weak transcription Genic enhancers Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs543681251	chr7:4817786-4817787	Weak transcription Genic enhancers Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs183267342	chr7:4817797-4817798	Weak transcription Genic enhancers Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs144887536	chr7:4817800-4817801	Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs201407809	chr7:4817824-4817825	Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs559376308	chr7:4817830-4817831	Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs186064772	chr7:4817853-4817854	Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs551522873	chr7:4817872-4817873	Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs569897591	chr7:4817876-4817877	Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs75146842	chr7:4817881-4817882	Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs547068592	chr7:4817913-4817914	Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs191660212	chr7:4817916-4817917	Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs549648435	chr7:4817920-4817921	Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs374245724	chr7:4817931-4817932	Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs183811959	chr7:4817932-4817933	Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs17135113	chr7:4817952-4817953	Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs553805221	chr7:4817981-4817982	Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs535183829	chr7:4818032-4818033	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs188297363	chr7:4818044-4818045	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs571729191	chr7:4818067-4818068	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs6975325	chr7:4818086-4818087	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs576301170	chr7:4818105-4818106	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs149041852	chr7:4818124-4818125	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs376012089	chr7:4818140-4818141	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs144649394	chr7:4818175-4818176	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs373863149	chr7:4818179-4818180	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs377223659	chr7:4818200-4818201	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs541390419	chr7:4818253-4818254	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs564351793	chr7:4818258-4818259	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs559336360	chr7:4818271-4818272	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs6979798	chr7:4818291-4818292	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs6955055	chr7:4818296-4818297	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs193009902	chr7:4818344-4818345	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200959987	chr7:4818391-4818392	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs60900888	chr7:4818396-4818397	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs182652252	chr7:4818470-4818471	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs549320668	chr7:4818588-4818589	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs419710	chr7:4818622-4818623	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs567901601	chr7:4818674-4818675	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs564736030	chr7:4818675-4818676	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs535023803	chr7:4818677-4818678	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs117420294	chr7:4818678-4818679	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs565658935	chr7:4818688-4818689	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	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
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Glioblastoma multiforme	21525872	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:228 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4816000-4820600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:4816000-4820600	Weak transcription	Small Intestine	intestine
3	chr7:4816000-4820800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr7:4816000-4820800	Weak transcription	Aorta	Aorta
5	chr7:4816000-4832000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr7:4816200-4817800	Weak transcription	Pancreas	Pancrea
7	chr7:4816200-4818200	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr7:4816200-4818200	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr7:4816200-4818200	Enhancers	Esophagus	oesophagus
10	chr7:4816200-4818200	Enhancers	Spleen	Spleen
11	chr7:4816200-4820400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr7:4816200-4820600	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr7:4816200-4820600	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr7:4816200-4820600	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr7:4816200-4820600	Weak transcription	HSMMtube	muscle
16	chr7:4816200-4820800	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr7:4816200-4820800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr7:4816200-4820800	Weak transcription	Fetal Lung	lung
19	chr7:4816200-4820800	Weak transcription	A549	lung
20	chr7:4816200-4821200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr7:4816200-4832000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr7:4816200-4834400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr7:4816400-4820400	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr7:4816400-4820800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr7:4816600-4817600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr7:4816600-4817600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr7:4816600-4817600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr7:4816600-4817600	Strong transcription	Fetal Muscle Trunk	muscle
29	chr7:4816600-4817600	Weak transcription	Right Ventricle	heart
30	chr7:4816600-4817800	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr7:4816600-4818000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr7:4816600-4818000	Weak transcription	Fetal Brain Male	brain
33	chr7:4816600-4818200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr7:4816600-4818200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr7:4816600-4818200	Enhancers	Adipose Nuclei	Adipose
36	chr7:4816600-4818200	Enhancers	Gastric	stomach
37	chr7:4816600-4818200	Enhancers	Lung	lung
38	chr7:4816600-4819400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr7:4816600-4820400	Weak transcription	Brain Germinal Matrix	brain
40	chr7:4816600-4820400	Weak transcription	Brain Hippocampus Middle	brain
41	chr7:4816600-4820600	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr7:4816600-4820600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr7:4816600-4820600	Weak transcription	Ovary	ovary
44	chr7:4816600-4820600	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr7:4816600-4820800	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr7:4816600-4822200	Weak transcription	Fetal Kidney	kidney
47	chr7:4816600-4830600	Weak transcription	Psoas Muscle	Psoas
48	chr7:4816600-4834800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr7:4816800-4817600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr7:4816800-4817800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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