Variant report

Variant	nsv916098
Chromosome Location	chr5:68824208-68902841
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:724)
CpG islands
(count:614)
Chromatin interactive
region (count:5)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:724 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:68856265-68856477	GM12878	blood:	n/a	n/a
2	BATF	chr5:68856954-68857395	GM12878	blood:	n/a	n/a
3	BATF	chr5:68857142-68857346	GM12878	blood:	n/a	n/a
4	BATF	chr5:68897794-68898185	GM12878	blood:	n/a	n/a
5	BATF	chr5:68897780-68898118	GM12878	blood:	n/a	n/a
6	BATF	chr5:68855769-68856236	GM12878	blood:	n/a	n/a
7	BATF	chr5:68855731-68856077	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:68897862-68898148	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:68857029-68857406	GM12878	blood:	n/a	n/a
10	BCL11A	chr5:68897742-68898263	GM12878	blood:	n/a	n/a
11	BCL11A	chr5:68855639-68856223	GM12878	blood:	n/a	chr5:68855979-68855988
12	BCL11A	chr5:68855749-68856242	GM12878	blood:	n/a	chr5:68855979-68855988
13	BCLAF1	chr5:68855724-68856116	K562	blood:	n/a	chr5:68855979-68855988
14	BCLAF1	chr5:68855724-68856135	GM12878	blood:	n/a	chr5:68855979-68855988
15	BCLAF1	chr5:68855724-68856111	K562	blood:	n/a	chr5:68855979-68855988
16	BCLAF1	chr5:68855732-68856164	GM12878	blood:	n/a	chr5:68855979-68855988
17	BHLHE40	chr5:68855820-68856132	HepG2	liver:	n/a	chr5:68855927-68855943 chr5:68855911-68855927
18	BRCA1	chr5:68855848-68856045	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr5:68855601-68856119	K562	blood:	n/a	n/a
20	CBX3	chr5:68855493-68856354	K562	blood:	n/a	n/a
21	CEBPB	chr5:68834691-68834785	HepG2	liver:	n/a	n/a
22	CEBPB	chr5:68834723-68834923	HepG2	liver:	n/a	n/a
23	CEBPB	chr5:68857201-68857397	K562	blood:	n/a	n/a
24	CEBPB	chr5:68855845-68856045	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr5:68857055-68857464	K562	blood:	n/a	n/a
26	CEBPD	chr5:68855760-68856284	K562	blood:	n/a	n/a
27	CHD2	chr5:68855844-68855949	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr5:68855923-68856048	GM12878	blood:	n/a	n/a
29	CHD2	chr5:68855853-68856047	Hela-S3	cervix:	n/a	n/a
30	CREB1	chr5:68855831-68856118	A549	lung:	n/a	n/a
31	CTCF	chr5:68855720-68855870	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr5:68855980-68856130	AG10803	skin:	n/a	n/a
33	CTCF	chr5:68855747-68855896	HepG2	liver:	n/a	n/a
34	CTCF	chr5:68855681-68856283	K562	blood:	n/a	n/a
35	CTCF	chr5:68855720-68855870	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr5:68855720-68855870	BJ	skin:	n/a	n/a
37	CTCF	chr5:68856000-68856150	RPTEC	kidney:	n/a	n/a
38	CTCF	chr5:68870569-68870638	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr5:68855980-68856130	Caco-2	colon:	n/a	n/a
40	CTCF	chr5:68855720-68855870	HAc	cerebellar:	n/a	n/a
41	CTCF	chr5:68855720-68855870	BE2_C	brain:	n/a	n/a
42	CTCF	chr5:68855980-68856130	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr5:68855720-68855870	HepG2	liver:	n/a	n/a
44	CTCF	chr5:68883919-68883967	Medullo	brain:	n/a	n/a
45	CTCF	chr5:68855958-68856060	HepG2	liver:	n/a	n/a
46	CTCF	chr5:68855783-68856107	GM10266	blood:	n/a	n/a
47	CTCF	chr5:68855720-68855870	RPTEC	kidney:	n/a	n/a
48	CTCF	chr5:68855980-68856130	GM12873	blood:	n/a	n/a
49	CTCF	chr5:68833712-68833856	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr5:68855846-68856040	GM19238	blood:	n/a	n/a

(count:614 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:68856065-68856115	HCF	heart:	n/a
2	chr5:68868293-68868343	HL-60	blood:	n/a
3	chr5:68855810-68855860	Caco-2	colon:	n/a
4	chr5:68855810-68855860	HMEC	breast:	n/a
5	chr5:68856065-68856115	HCF	heart:	n/a
6	chr5:68868293-68868343	HL-60	blood:	n/a
7	chr5:68855810-68855860	Caco-2	colon:	n/a
8	chr5:68855810-68855860	HMEC	breast:	n/a
9	chr5:68852996-68853046	HNPCEpiC	eye:	n/a
10	chr5:68856062-68856112	LNCaP	prostate:	n/a
11	chr5:68868293-68868343	GM19239	blood:	n/a
12	chr5:68857760-68857810	HEEpiC	esophagus:	n/a
13	chr5:68859882-68859932	BE2_C	brain:	n/a
14	chr5:68856062-68856112	NB4	blood:	n/a
15	chr5:68857760-68857810	Caco-2	colon:	n/a
16	chr5:68859882-68859932	GM06990	blood:	n/a
17	chr5:68856065-68856115	HUVEC	blood vessel:	n/a
18	chr5:68852996-68853046	BE2_C	brain:	n/a
19	chr5:68855873-68855923	MCF-7	breast:	n/a
20	chr5:68855560-68855610	Hepatocyte	liver:	n/a
21	chr5:68856077-68856127	SK-N-MC	brain:	n/a
22	chr5:68856062-68856112	Jurkat	blood:	n/a
23	chr5:68852996-68853046	Hela-S3	cervix:	n/a
24	chr5:68857760-68857810	SK-N-MC	brain:	n/a
25	chr5:68857760-68857810	MCF10A-Er-Src	breast:	n/a
26	chr5:68856065-68856115	CMK	blood:	n/a
27	chr5:68857760-68857810	ovcar-3	ovarian:	n/a
28	chr5:68857760-68857810	HRE	kidney:	n/a
29	chr5:68859882-68859932	BJ	skin:	n/a
30	chr5:68868293-68868343	AoSMC	blood vessel:	n/a
31	chr5:68855873-68855923	T-47D	breast:	n/a
32	chr5:68857760-68857810	HL-60	blood:	n/a
33	chr5:68856077-68856127	PFSK-1	brain:	n/a
34	chr5:68855560-68855610	LNCaP	prostate:	n/a
35	chr5:68856065-68856115	RPTEC	kidney:	n/a
36	chr5:68856077-68856127	K562	blood:	n/a
37	chr5:68856077-68856127	HCPEpiC	choroid plexus:	n/a
38	chr5:68855810-68855860	AG04449	skin:	fetal
39	chr5:68855560-68855610	PrEC	prostate:	n/a
40	chr5:68855873-68855923	GM06990	blood:	n/a
41	chr5:68856065-68856115	HCPEpiC	choroid plexus:	n/a
42	chr5:68855810-68855860	HCM	heart:	n/a
43	chr5:68868293-68868343	Caco-2	colon:	n/a
44	chr5:68859882-68859932	HAEpiC	amniotic membrane:	n/a
45	chr5:68856062-68856112	AG10803	skin:	n/a
46	chr5:68856077-68856127	Jurkat	blood:	n/a
47	chr5:68868293-68868343	AG10803	skin:	n/a
48	chr5:68856065-68856115	HIPEpiC	eye:	n/a
49	chr5:68856065-68856115	LNCaP	prostate:	n/a
50	chr5:68855810-68855860	NT2-D1	testis:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:68786843..68790127-chr5:68821932..68828319,7	MCF-7	breast:
2	chr5:68811437..68815245-chr5:68822688..68826346,4	MCF-7	breast:
3	chr5:68791729..68794377-chr5:68827769..68829901,2	MCF-7	breast:
4	chr5:68787211..68792044-chr5:68819088..68825852,9	MCF-7	breast:
5	chr5:68711082..68712894-chr5:68825364..68828331,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OCLN-1	chr5:68860927-68860960	NONHSAT101929
2	lnc-GTF2H2C-1	chr5:68889300-68889532	NONHSAT101931
3	lnc-GTF2H2C-1	chr5:68890071-68890550	NONHSAT101931
4	lnc-OCLN-1	chr5:68858500-68858597	NONHSAT101929
5	lnc-OCLN-1	chr5:68856086-68856428	NONHSAT101929

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GTF2H2D	hsa-miR-30a-5p	chr5:68888221-68888242

Variant related genes	Relation type
ENSG00000238740	TF binding region
OCLN	TF binding region
ENSG00000248477	TF binding region
GTF2H2C	TF binding region
RNU6-724P	TF binding region
ENSG00000238740	CpG island
OCLN	CpG island
ENSG00000248477	CpG island
GTF2H2C	CpG island
RNU6-724P	CpG island
ENSG00000197822	chromatin interactions
ENSG00000152939	chromatin interactions

Extended variants
information (count: 766 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:766 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541756685	chr5:68824212-68824213	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs144449146	chr5:68824230-68824231	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs202202842	chr5:68824238-68824239	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs200486327	chr5:68824239-68824240	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs201233073	chr5:68824240-68824241	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs28562181	chr5:68824310-68824311	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs572280536	chr5:68824321-68824322	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs545974778	chr5:68824398-68824399	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs191432040	chr5:68824447-68824448	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs184683383	chr5:68824463-68824464	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs569099850	chr5:68824602-68824603	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs536546744	chr5:68824607-68824608	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs77441195	chr5:68824650-68824651	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs78039662	chr5:68824670-68824671	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs560633719	chr5:68824717-68824718	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs529630640	chr5:68824731-68824732	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs547782723	chr5:68824753-68824754	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs565983629	chr5:68824777-68824778	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs200207586	chr5:68824864-68824865	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs79890525	chr5:68824865-68824866	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs35628909	chr5:68824886-68824887	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs35591695	chr5:68824966-68824967	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs537128882	chr5:68825018-68825019	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs555780095	chr5:68825020-68825021	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs567544348	chr5:68825033-68825034	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs368715911	chr5:68825057-68825058	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs190747184	chr5:68825081-68825082	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs533891296	chr5:68825085-68825086	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs116619691	chr5:68825094-68825095	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs576991183	chr5:68825125-68825126	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs572342617	chr5:68825143-68825144	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs547768628	chr5:68825202-68825203	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs181674456	chr5:68825281-68825282	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs74738319	chr5:68825345-68825346	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs186833078	chr5:68825348-68825349	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs138094927	chr5:68825358-68825359	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs536292271	chr5:68825416-68825417	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs190070041	chr5:68825419-68825420	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs540990770	chr5:68825450-68825451	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs559632439	chr5:68825493-68825494	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs112124394	chr5:68825495-68825496	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs551590570	chr5:68825513-68825514	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs181121712	chr5:68825570-68825571	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs570081072	chr5:68825597-68825598	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs145957494	chr5:68825657-68825658	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs549220593	chr5:68825685-68825686	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs567706489	chr5:68825720-68825721	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs138877569	chr5:68825721-68825722	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs185862446	chr5:68825770-68825771	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs116382845	chr5:68825923-68825924	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:112)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ovarian cancer	21781307	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
abnormal development	18461090	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21045282	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelodysplastic syndrome	18663149	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Sezary syndrome	18413736	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21990379	CNVD
Hirschsprung''s Disease	21712996	CNVD
Apoptosis	19488400	CNVD
Breast cancer	22048815	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Acute monocytic leukemia	16498392	CNVD
Colorectal cancer	20459617	CNVD
Gastric adenocarcinoma	19115996	CNVD
Spinal muscular atrophy	17160897	CNVD
Spinal muscular atrophy	17668391	CNVD
Spinal muscular atrophy	17668395	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pseudo-TORCH syndrome	20727516	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD

Chromatin state (count:458 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68790200-68824600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:68805600-68826200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr5:68805600-68826600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr5:68806400-68826400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr5:68815400-68826600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr5:68815800-68831000	Weak transcription	HepG2	liver
7	chr5:68817200-68827200	Weak transcription	GM12878-XiMat	blood
8	chr5:68819800-68824600	Genic enhancers	Fetal Intestine Small	intestine
9	chr5:68821800-68830800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr5:68822200-68826800	Weak transcription	Lung	lung
11	chr5:68822400-68829400	Weak transcription	Fetal Stomach	stomach
12	chr5:68822600-68824400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:68822600-68826200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr5:68822800-68826400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr5:68822800-68826800	Weak transcription	Gastric	stomach
16	chr5:68822800-68828000	Weak transcription	Liver	Liver
17	chr5:68823000-68824400	Enhancers	Stomach Mucosa	stomach
18	chr5:68823200-68824800	Enhancers	Placenta	Placenta
19	chr5:68823400-68824400	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr5:68823400-68824400	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr5:68823600-68824400	Enhancers	NHEK	skin
22	chr5:68823600-68825200	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr5:68823600-68829200	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr5:68823800-68826600	Weak transcription	Pancreas	Pancrea
25	chr5:68824000-68826000	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr5:68824000-68827000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr5:68824000-68830600	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr5:68824000-68855400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr5:68824200-68824400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr5:68824200-68824600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr5:68824200-68824800	Genic enhancers	Fetal Intestine Large	intestine
32	chr5:68824200-68826600	Weak transcription	Duodenum Mucosa	Duodenum
33	chr5:68824200-68829600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr5:68824400-68824600	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr5:68824400-68824800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr5:68824400-68826000	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr5:68824400-68826200	Weak transcription	Stomach Mucosa	stomach
38	chr5:68824400-68832400	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr5:68824600-68824800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr5:68824600-68825000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr5:68824600-68825200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr5:68824600-68825800	Strong transcription	Fetal Intestine Small	intestine
43	chr5:68824800-68825600	Strong transcription	Fetal Intestine Large	intestine
44	chr5:68824800-68826600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr5:68824800-68827000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr5:68825000-68825200	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr5:68825200-68826400	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr5:68825200-68826800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr5:68825200-68827200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr5:68825600-68826000	Weak transcription	Fetal Intestine Large	intestine

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