Variant report

Variant	esv2762516
Chromosome Location	chr5:36599385-36613201
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:36606645-36607176	GM12878	blood:	n/a	n/a
2	BRCA1	chr5:36606267-36607563	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr5:36608205-36608500	HepG2	liver:	n/a	chr5:36608334-36608347 chr5:36608334-36608345 chr5:36608334-36608347 chr5:36608335-36608346
4	CEBPB	chr5:36608137-36608601	ECC-1	luminal epithelium:	n/a	chr5:36608334-36608347 chr5:36608334-36608345 chr5:36608334-36608347 chr5:36608335-36608346
5	CEBPB	chr5:36607203-36607469	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr5:36608115-36608572	MCF-7	breast:	n/a	chr5:36608334-36608347 chr5:36608334-36608345 chr5:36608334-36608347 chr5:36608335-36608346
7	CEBPB	chr5:36606309-36607740	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr5:36611876-36612146	Hela-S3	cervix:	n/a	chr5:36611990-36611999 chr5:36611880-36611892 chr5:36611990-36611999 chr5:36611988-36612001 chr5:36611990-36611999 chr5:36611990-36611999 chr5:36611990-36612001
9	CEBPB	chr5:36607944-36608821	Hela-S3	cervix:	n/a	chr5:36608334-36608347 chr5:36608334-36608345 chr5:36608334-36608347 chr5:36608335-36608346
10	CEBPB	chr5:36608176-36608437	IMR90	lung:	n/a	chr5:36608334-36608347 chr5:36608334-36608345 chr5:36608334-36608347 chr5:36608335-36608346
11	CEBPB	chr5:36608167-36608523	ECC-1	luminal epithelium:	n/a	chr5:36608334-36608347 chr5:36608334-36608345 chr5:36608334-36608347 chr5:36608335-36608346
12	CEBPB	chr5:36608055-36608520	H1-hESC	embryonic stem cell:	n/a	chr5:36608334-36608347 chr5:36608334-36608345 chr5:36608334-36608347 chr5:36608335-36608346
13	CEBPB	chr5:36608320-36608452	K562	blood:	n/a	chr5:36608334-36608347 chr5:36608334-36608345 chr5:36608334-36608347 chr5:36608335-36608346
14	CEBPB	chr5:36611883-36612134	K562	blood:	n/a	chr5:36611990-36611999 chr5:36611990-36611999 chr5:36611988-36612001 chr5:36611990-36611999 chr5:36611990-36611999 chr5:36611990-36612001
15	CHD1	chr5:36606705-36607462	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD1	chr5:36608026-36608090	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr5:36606508-36607088	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr5:36608191-36608482	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr5:36606467-36607538	Hela-S3	cervix:	n/a	n/a
20	CREB1	chr5:36607258-36607511	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr5:36608320-36608470	HCPEpiC	choroid plexus:	n/a	chr5:36608388-36608397
22	CTCF	chr5:36602767-36603223	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr5:36602920-36603070	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr5:36602860-36603010	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr5:36602940-36603090	GM12878	blood:	n/a	n/a
26	CTCF	chr5:36602871-36603164	K562	blood:	n/a	n/a
27	CTCF	chr5:36602836-36603198	GM12878	blood:	n/a	n/a
28	CTCF	chr5:36603100-36603250	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr5:36602900-36603050	AG04449	skin:	n/a	n/a
30	CTCF	chr5:36602900-36603050	RPTEC	kidney:	n/a	n/a
31	CTCF	chr5:36603080-36603230	GM12864	blood:	n/a	n/a
32	CTCF	chr5:36602910-36603097	GM12892	blood:	n/a	n/a
33	CTCF	chr5:36602969-36603063	Lung_OC	lung:	n/a	n/a
34	CTCF	chr5:36602900-36603050	GM12871	blood:	n/a	n/a
35	CTCF	chr5:36608200-36608350	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr5:36602893-36603103	GM10266	blood:	n/a	n/a
37	CTCF	chr5:36602920-36603070	Caco-2	colon:	n/a	n/a
38	CTCF	chr5:36602920-36603070	BJ	skin:	n/a	n/a
39	CTCF	chr5:36603000-36603150	HCT-116	colon:	n/a	n/a
40	CTCF	chr5:36602875-36603123	GM19238	blood:	n/a	n/a
41	CTCF	chr5:36602880-36603030	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr5:36606718-36606771	MCF-7	breast:	n/a	n/a
43	CTCF	chr5:36602880-36603030	GM12869	blood:	n/a	n/a
44	CTCF	chr5:36602900-36603115	MCF-7	breast:	n/a	n/a
45	CTCF	chr5:36602920-36603070	GM12865	blood:	n/a	n/a
46	CTCF	chr5:36602920-36603070	HPF	lung:	n/a	n/a
47	CTCF	chr5:36602894-36603071	HepG2	liver:	n/a	n/a
48	CTCF	chr5:36602940-36603090	GM12873	blood:	n/a	n/a
49	CTCF	chr5:36602820-36602970	NHEK	skin:	n/a	n/a
50	CTCF	chr5:36602920-36603070	GM12873	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:36607065-36607115	GM19239	blood:	n/a
2	chr5:36607065-36607115	GM19239	blood:	n/a
3	chr5:36606601-36606651	A549	lung:	n/a
4	chr5:36607024-36607074	HPAEpiC	pulmonary alveolar:	n/a
5	chr5:36606293-36606343	PANC-1	pancreas:	n/a
6	chr5:36606749-36606799	AG09319	gingival:	n/a
7	chr5:36608769-36608819	HCPEpiC	choroid plexus:	n/a
8	chr5:36606756-36606806	HepG2	liver:	n/a
9	chr5:36606520-36606570	HUVEC	blood vessel:	n/a
10	chr5:36606293-36606343	SK-N-SH_RA	brain:	n/a
11	chr5:36606981-36607031	AG09319	gingival:	n/a
12	chr5:36607377-36607427	HRPEpiC	eye:	n/a
13	chr5:36606795-36606845	HepG2	liver:	n/a
14	chr5:36606769-36606819	Hepatocyte	liver:	n/a
15	chr5:36608598-36608648	A549	lung:	n/a
16	chr5:36607390-36607440	AG09319	gingival:	n/a
17	chr5:36606446-36606496	AG09309	skin:	n/a
18	chr5:36607333-36607383	HEEpiC	esophagus:	n/a
19	chr5:36608598-36608648	ovcar-3	ovarian:	n/a
20	chr5:36606601-36606651	HPAEpiC	pulmonary alveolar:	n/a
21	chr5:36606894-36606944	Hepatocyte	liver:	n/a
22	chr5:36607024-36607074	HEK293	kidney:	embryo
23	chr5:36607417-36607467	NB4	blood:	n/a
24	chr5:36608769-36608819	K562	blood:	n/a
25	chr5:36607390-36607440	HEK293	kidney:	embryo
26	chr5:36606756-36606806	HL-60	blood:	n/a
27	chr5:36606894-36606944	GM12892	blood:	n/a
28	chr5:36606769-36606819	HRCEpiC	kidney:	n/a
29	chr5:36607333-36607383	CMK	blood:	n/a
30	chr5:36608598-36608648	HRE	kidney:	n/a
31	chr5:36606520-36606570	MCF-7	breast:	n/a
32	chr5:36606795-36606845	PrEC	prostate:	n/a
33	chr5:36606446-36606496	IMR90	lung:	fetal
34	chr5:36607390-36607440	HPAEpiC	pulmonary alveolar:	n/a
35	chr5:36608769-36608819	NT2-D1	testis:	n/a
36	chr5:36606102-36606152	AG10803	skin:	n/a
37	chr5:36606347-36606397	MCF-7	breast:	n/a
38	chr5:36608769-36608819	Caco-2	colon:	n/a
39	chr5:36606756-36606806	HEEpiC	esophagus:	n/a
40	chr5:36608598-36608648	AG10803	skin:	n/a
41	chr5:36606795-36606845	BE2_C	brain:	n/a
42	chr5:36606102-36606152	HepG2	liver:	n/a
43	chr5:36606756-36606806	HRCEpiC	kidney:	n/a
44	chr5:36606749-36606799	HCM	heart:	n/a
45	chr5:36607390-36607440	HepG2	liver:	n/a
46	chr5:36607333-36607383	HL-60	blood:	n/a
47	chr5:36607390-36607440	NT2-D1	testis:	n/a
48	chr5:36606981-36607031	HCF	heart:	n/a
49	chr5:36606795-36606845	GM12892	blood:	n/a
50	chr5:36607390-36607440	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:247170899..247171471-chr5:36606529..36607214,2	Hela-S3	cervix:
2	chr5:36607368..36609529-chr5:36613052..36615679,2	MCF-7	breast:
3	chr11:32851420..32852136-chr5:36606640..36607218,2	Hela-S3	cervix:
4	chr5:36598036..36602737-chr5:36604248..36607271,4	K562	blood:
5	chr17:75136212..75137144-chr5:36606465..36607208,2	Hela-S3	cervix:
6	chr17:74733057..74733878-chr5:36606716..36607710,2	Hela-S3	cervix:
7	chr15:73925518..73926026-chr5:36606661..36607602,2	Hela-S3	cervix:
8	chr15:50716373..50717091-chr5:36606437..36607181,2	Hela-S3	cervix:
9	chr5:36602958..36603570-chr5:36688895..36689448,2	MCF-7	breast:
10	chr5:36602536..36603410-chr5:36692728..36693815,5	MCF-7	breast:
11	chr5:36607368..36609529-chr5:36613052..36615679,2	MCF-7	breast:
12	chr5:36602570..36603716-chr5:36690159..36691138,5	MCF-7	breast:
13	chr5:36602557..36603415-chr5:36695863..36696651,3	MCF-7	breast:
14	chr16:14726780..14727283-chr5:36606489..36607214,2	Hela-S3	cervix:
15	chr1:210547064..210548029-chr5:36606437..36607100,2	Hela-S3	cervix:

Variant related genes	Relation type
SLC1A3	TF binding region
SLC1A3	CpG island
ENSG00000129657	chromatin interactions
ENSG00000092931	chromatin interactions
ENSG00000103429	chromatin interactions
ENSG00000156642	chromatin interactions
ENSG00000197472	chromatin interactions
ENSG00000200972	chromatin interactions
ENSG00000161547	chromatin interactions
ENSG00000138592	chromatin interactions
ENSG00000079215	chromatin interactions
ENSG00000135378	chromatin interactions

Extended variants
information (count: 553 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:553 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2562573	chr5:36599385-36599386	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs532711917	chr5:36599428-36599429	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs552712040	chr5:36599503-36599504	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs369636426	chr5:36599508-36599509	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs527425043	chr5:36599538-36599539	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs148746664	chr5:36599548-36599549	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs570655338	chr5:36599559-36599560	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs371999168	chr5:36599610-36599611	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs397997372	chr5:36599629-36599630	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs2731876	chr5:36599631-36599632	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs538112340	chr5:36599635-36599636	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs550116028	chr5:36599646-36599647	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs568425434	chr5:36599650-36599651	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs12173042	chr5:36599665-36599666	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs375063085	chr5:36599676-36599677	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs557801083	chr5:36599694-36599695	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs557421091	chr5:36599760-36599761	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs554184817	chr5:36599761-36599762	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs191964391	chr5:36599766-36599767	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs531795316	chr5:36599769-36599770	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs539956302	chr5:36599776-36599777	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs34065809	chr5:36599803-36599804	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs117192682	chr5:36599869-36599870	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs147017447	chr5:36599873-36599874	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs117426421	chr5:36599942-36599943	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs12173139	chr5:36599946-36599947	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs77725245	chr5:36599960-36599961	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs147646385	chr5:36599988-36599989	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs61274624	chr5:36600010-36600011	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs560130782	chr5:36600048-36600049	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs576067692	chr5:36600072-36600073	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs371621200	chr5:36600088-36600089	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs552274206	chr5:36600095-36600096	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs564093937	chr5:36600193-36600194	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs531547077	chr5:36600204-36600205	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs541988158	chr5:36600411-36600412	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs568361214	chr5:36600414-36600415	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs373383084	chr5:36600427-36600428	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs535789881	chr5:36600457-36600458	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs140810202	chr5:36600491-36600492	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs369571601	chr5:36600494-36600495	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs150142438	chr5:36600500-36600501	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs566092744	chr5:36600503-36600504	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs78143277	chr5:36600530-36600531	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs76591410	chr5:36600558-36600559	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs576186618	chr5:36600568-36600569	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs537247209	chr5:36600578-36600579	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs566725292	chr5:36600583-36600584	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs138416776	chr5:36600617-36600618	Genic enhancers Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs7730144	chr5:36600633-36600634	Genic enhancers Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:99)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	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
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:718 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36591200-36606200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:36597000-36600400	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr5:36597000-36603000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr5:36597000-36605600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr5:36597000-36606200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr5:36597200-36600400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr5:36597200-36600400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr5:36597200-36601000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr5:36597200-36605200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr5:36597800-36600000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr5:36598000-36600600	Weak transcription	Fetal Kidney	kidney
12	chr5:36598200-36600200	Weak transcription	Fetal Lung	lung
13	chr5:36598200-36603000	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr5:36598200-36603000	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr5:36598400-36600000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr5:36598400-36600000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr5:36598400-36600200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr5:36598400-36600600	Weak transcription	Adipose Nuclei	Adipose
19	chr5:36598400-36603000	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr5:36598400-36603200	Weak transcription	Fetal Muscle Leg	muscle
21	chr5:36598400-36604400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr5:36598600-36600000	Weak transcription	Brain Anterior Caudate	brain
23	chr5:36598600-36600200	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr5:36598600-36600200	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr5:36598800-36600000	Weak transcription	Brain Angular Gyrus	brain
26	chr5:36599000-36600200	Weak transcription	Brain Germinal Matrix	brain
27	chr5:36599000-36600200	Weak transcription	Brain Substantia Nigra	brain
28	chr5:36599200-36599400	Enhancers	Brain Hippocampus Middle	brain
29	chr5:36599200-36600600	Enhancers	Brain Cingulate Gyrus	brain
30	chr5:36599400-36600200	Weak transcription	Brain Hippocampus Middle	brain
31	chr5:36600000-36600200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr5:36600000-36600400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr5:36600000-36601000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr5:36600000-36601200	Enhancers	Osteobl	bone
35	chr5:36600000-36602200	Enhancers	Brain Anterior Caudate	brain
36	chr5:36600000-36604200	Enhancers	Brain Angular Gyrus	brain
37	chr5:36600000-36605600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr5:36600200-36600400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr5:36600200-36600600	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr5:36600200-36600600	Enhancers	NH-A	brain
41	chr5:36600200-36600800	Enhancers	Brain Hippocampus Middle	brain
42	chr5:36600200-36601000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr5:36600200-36601200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr5:36600200-36601200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr5:36600200-36601200	Enhancers	HMEC	breast
46	chr5:36600200-36601200	Enhancers	NHEK	skin
47	chr5:36600200-36601800	Enhancers	Fetal Lung	lung
48	chr5:36600200-36602200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
49	chr5:36600200-36602200	Enhancers	Fetal Brain Male	brain
50	chr5:36600200-36602600	Enhancers	Brain Germinal Matrix	brain

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