Variant report

Variant	nsv518282
Chromosome Location	chr4:8611176-8620464
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:77)
CpG islands
(count:427)
Chromatin interactive
region (count:2)
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	BCL3	chr4:8612532-8612922	GM12878	blood:	n/a	n/a
2	EBF1	chr4:8611309-8611598	GM12878	blood:	n/a	chr4:8611440-8611450 chr4:8611439-8611450
3	FOS	chr4:8612303-8612533	MCF10A-Er-Src	breast:	n/a	n/a
4	FOS	chr4:8612302-8612525	MCF10A-Er-Src	breast:	n/a	n/a
5	GATA2	chr4:8617634-8618325	SH-SY5Y	brain:	n/a	chr4:8617915-8617927
6	GATA3	chr4:8617667-8618175	SH-SY5Y	brain:	n/a	chr4:8617915-8617927
7	HMGN3	chr4:8618868-8618870	K562	blood:	n/a	n/a
8	HMGN3	chr4:8615965-8616094	K562	blood:	n/a	n/a
9	HMGN3	chr4:8615509-8615520	K562	blood:	n/a	n/a
10	NFATC1	chr4:8612550-8612964	GM12878	blood:	n/a	n/a
11	PBX3	chr4:8612627-8612860	GM12878	blood:	n/a	n/a
12	POLR2A	chr4:8611479-8612417	H1-hESC	embryonic stem cell:	n/a	n/a
13	POLR2A	chr4:8614457-8614635	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr4:8612044-8612227	MCF-7	breast:	n/a	n/a
15	POLR2A	chr4:8616241-8616451	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr4:8609210-8612749	PFSK-1	brain:	n/a	n/a
17	POLR2A	chr4:8612760-8612766	MCF-7	breast:	n/a	n/a
18	POLR2A	chr4:8619958-8620173	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr4:8609192-8612704	HEK293	kidney:	n/a	n/a
20	POLR2A	chr4:8617165-8617336	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr4:8617102-8622051	K562	blood:	n/a	n/a
22	POLR2A	chr4:8618729-8618753	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr4:8617489-8617528	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr4:8618361-8618654	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr4:8611388-8612452	Hela-S3	cervix:	n/a	n/a
26	POLR2A	chr4:8615153-8615313	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr4:8612808-8613143	HCT-116	colon:	n/a	n/a
28	POLR2A	chr4:8611427-8611724	HCT-116	colon:	n/a	n/a
29	POLR2A	chr4:8613070-8613073	MCF-7	breast:	n/a	n/a
30	POLR2A	chr4:8611259-8614817	K562	blood:	n/a	n/a
31	POLR2A	chr4:8612532-8613323	PFSK-1	brain:	n/a	n/a
32	POLR2A	chr4:8612391-8612614	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr4:8612399-8612715	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr4:8612765-8613102	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr4:8613442-8613689	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr4:8613303-8613523	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr4:8613055-8613237	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr4:8616295-8616342	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr4:8611916-8612278	HCT-116	colon:	n/a	n/a
40	POLR2A	chr4:8614367-8614678	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr4:8612857-8613401	PFSK-1	brain:	n/a	n/a
42	POLR2A	chr4:8616006-8616274	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr4:8616866-8617114	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr4:8613163-8613164	MCF-7	breast:	n/a	n/a
45	POLR2A	chr4:8611276-8611298	ProgFib	skin:	n/a	n/a
46	POLR2A	chr4:8617538-8617573	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr4:8620063-8620430	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr4:8618597-8618951	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr4:8619363-8619768	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr4:8613104-8613130	MCF-7	breast:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8620162-8620212	Jurkat	blood:	n/a
2	chr4:8620162-8620212	RPTEC	kidney:	n/a
3	chr4:8619939-8619989	HRPEpiC	eye:	n/a
4	chr4:8617738-8617788	BJ	skin:	n/a
5	chr4:8620162-8620212	AG09309	skin:	n/a
6	chr4:8615996-8616046	HUVEC	blood vessel:	n/a
7	chr4:8616045-8616095	SK-N-SH	brain:	n/a
8	chr4:8619939-8619989	AG09309	skin:	n/a
9	chr4:8619939-8619989	GM12891	blood:	n/a
10	chr4:8617839-8617889	LNCaP	prostate:	n/a
11	chr4:8617839-8617889	AG04449	skin:	fetal
12	chr4:8619939-8619989	ovcar-3	ovarian:	n/a
13	chr4:8617910-8617960	AG09309	skin:	n/a
14	chr4:8617738-8617788	AG10803	skin:	n/a
15	chr4:8615996-8616046	HAEpiC	amniotic membrane:	n/a
16	chr4:8617738-8617788	AoSMC	blood vessel:	n/a
17	chr4:8616045-8616095	U87	brain:	n/a
18	chr4:8619939-8619989	GM12878	blood:	n/a
19	chr4:8619939-8619989	SK-N-MC	brain:	n/a
20	chr4:8617738-8617788	HCM	heart:	n/a
21	chr4:8620162-8620212	AoSMC	blood vessel:	n/a
22	chr4:8615996-8616046	T-47D	breast:	n/a
23	chr4:8617839-8617889	A549	lung:	n/a
24	chr4:8617910-8617960	HRE	kidney:	n/a
25	chr4:8615996-8616046	HIPEpiC	eye:	n/a
26	chr4:8615996-8616046	AG04449	skin:	fetal
27	chr4:8617839-8617889	H1-hESC	embryonic stem cell:	embryo
28	chr4:8617839-8617889	NHDF-neo	bronchial:	n/a
29	chr4:8616045-8616095	SK-N-MC	brain:	n/a
30	chr4:8616045-8616095	IMR90	lung:	fetal
31	chr4:8617910-8617960	NHDF-neo	bronchial:	n/a
32	chr4:8617738-8617788	HEK293	kidney:	embryo
33	chr4:8616045-8616095	HNPCEpiC	eye:	n/a
34	chr4:8617839-8617889	Hela-S3	cervix:	n/a
35	chr4:8617839-8617889	MCF10A-Er-Src	breast:	n/a
36	chr4:8619939-8619989	BJ	skin:	n/a
37	chr4:8619939-8619989	H1-hESC	embryonic stem cell:	embryo
38	chr4:8619939-8619989	NHDF-neo	bronchial:	n/a
39	chr4:8617738-8617788	GM19239	blood:	n/a
40	chr4:8619939-8619989	HCT-116	colon:	n/a
41	chr4:8617910-8617960	MCF-7	breast:	n/a
42	chr4:8616045-8616095	MCF10A-Er-Src	breast:	n/a
43	chr4:8619939-8619989	MCF10A-Er-Src	breast:	n/a
44	chr4:8619939-8619989	RPTEC	kidney:	n/a
45	chr4:8619939-8619989	LNCaP	prostate:	n/a
46	chr4:8616045-8616095	ovcar-3	ovarian:	n/a
47	chr4:8617738-8617788	HRPEpiC	eye:	n/a
48	chr4:8615996-8616046	HEEpiC	esophagus:	n/a
49	chr4:8620162-8620212	NHBE	bronchial:	n/a
50	chr4:8615996-8616046	SK-N-SH_RA	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:8607464..8609784-chr4:8610863..8613633,2	MCF-7	breast:
2	chr4:8617932..8619527-chr4:8918338..8920672,2	MCF-7	breast:

No data

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

Extended variants
information (count: 941 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:941 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4696715	chr4:8611176-8611177	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs7692629	chr4:8611197-8611198	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs532897787	chr4:8611210-8611211	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs35322306	chr4:8611243-8611244	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs111905918	chr4:8611244-8611245	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556955283	chr4:8611258-8611259	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs146230210	chr4:8611259-8611260	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190351053	chr4:8611260-8611261	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs139299195	chr4:8611276-8611277	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs182039164	chr4:8611301-8611302	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184267359	chr4:8611328-8611329	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538504768	chr4:8611335-8611336	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556301230	chr4:8611339-8611340	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189079057	chr4:8611343-8611344	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545548316	chr4:8611349-8611350	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs554305663	chr4:8611350-8611351	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573116333	chr4:8611353-8611354	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs112090009	chr4:8611366-8611367	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs139542035	chr4:8611371-8611372	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529189062	chr4:8611377-8611378	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs544478816	chr4:8611380-8611381	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562170662	chr4:8611383-8611384	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532762251	chr4:8611394-8611395	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551098860	chr4:8611398-8611399	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541799049	chr4:8611403-8611404	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs532961926	chr4:8611405-8611406	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs7674757	chr4:8611409-8611410	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs527335347	chr4:8611412-8611413	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs572976524	chr4:8611419-8611420	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs149975934	chr4:8611424-8611425	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs567815979	chr4:8611439-8611440	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs112044489	chr4:8611440-8611441	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs148785945	chr4:8611443-8611444	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs571717692	chr4:8611448-8611449	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs539027131	chr4:8611451-8611452	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs542891946	chr4:8611466-8611467	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs554168938	chr4:8611488-8611489	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs370958953	chr4:8611490-8611491	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs560140215	chr4:8611518-8611519	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs11736030	chr4:8611528-8611529	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs536724127	chr4:8611530-8611531	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs555306837	chr4:8611531-8611532	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs573757958	chr4:8611535-8611536	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs531937290	chr4:8611561-8611562	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs181089264	chr4:8611577-8611578	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs371582102	chr4:8611583-8611584	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs3796733	chr4:8611600-8611601	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs3796732	chr4:8611645-8611646	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs375427547	chr4:8611663-8611664	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs3796731	chr4:8611664-8611665	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Melanoma	20688739	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8596000-8622800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:8596000-8623200	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr4:8597600-8618400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr4:8599600-8616000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr4:8601200-8611400	Weak transcription	Spleen	Spleen
6	chr4:8601400-8616000	Weak transcription	HSMMtube	muscle
7	chr4:8601600-8620200	Weak transcription	NHDF-Ad	bronchial
8	chr4:8601800-8617000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr4:8601800-8622000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr4:8603200-8615400	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr4:8605800-8612000	Weak transcription	Gastric	stomach
12	chr4:8606800-8615400	Weak transcription	Osteobl	bone
13	chr4:8607800-8616000	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr4:8608000-8613000	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr4:8608400-8614200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr4:8609600-8612000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr4:8609800-8611200	Weak transcription	Adipose Nuclei	Adipose
18	chr4:8609800-8615200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr4:8610200-8611800	Strong transcription	H1 Cell Line	embryonic stem cell
20	chr4:8610400-8611600	Weak transcription	GM12878-XiMat	blood
21	chr4:8610400-8618800	Strong transcription	Ovary	ovary
22	chr4:8610400-8620400	Weak transcription	Right Atrium	heart
23	chr4:8610400-8622000	Strong transcription	Placenta	Placenta
24	chr4:8610600-8611400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr4:8611200-8613400	Enhancers	Adipose Nuclei	Adipose
26	chr4:8611400-8611800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
27	chr4:8611400-8611800	ZNF genes & repeats	Spleen	Spleen
28	chr4:8611400-8613000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr4:8611600-8612000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
30	chr4:8611600-8612200	Enhancers	GM12878-XiMat	blood
31	chr4:8611600-8613000	Enhancers	Esophagus	oesophagus
32	chr4:8611800-8614200	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr4:8611800-8620400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr4:8611800-8622000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr4:8611800-8622800	Weak transcription	Spleen	Spleen
36	chr4:8612000-8612200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr4:8612000-8612600	Active TSS	Gastric	stomach
38	chr4:8612000-8614800	Enhancers	Left Ventricle	heart
39	chr4:8612200-8612800	Enhancers	Right Ventricle	heart
40	chr4:8612200-8613600	Enhancers	Skeletal Muscle Male	skeletal muscle
41	chr4:8612800-8613000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
42	chr4:8612800-8613600	Weak transcription	Right Ventricle	heart
43	chr4:8613000-8613200	Bivalent Enhancer	Fetal Stomach	stomach
44	chr4:8613000-8613800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
45	chr4:8613000-8613800	Enhancers	Lung	lung
46	chr4:8613000-8614400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr4:8613000-8617200	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr4:8613000-8617600	Strong transcription	Placenta Amnion	Placenta Amnion
49	chr4:8613000-8623000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr4:8613400-8613600	Enhancers	Rectal Mucosa Donor 31	rectum

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