Variant report

Variant	nsv881383
Chromosome Location	chr5:37485316-37773877
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2669)
CpG islands
(count:428)
Chromatin interactive
region (count:109)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2669 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:37554224-37554305	K562	blood:	n/a	n/a
2	ARID3A	chr5:37561556-37561928	K562	blood:	n/a	n/a
3	ARID3A	chr5:37566412-37566482	K562	blood:	n/a	n/a
4	ARID3A	chr5:37576244-37577007	K562	blood:	n/a	chr5:37576689-37576705 chr5:37576688-37576704
5	ARID3A	chr5:37723608-37723756	K562	blood:	n/a	n/a
6	ARID3A	chr5:37758290-37758411	K562	blood:	n/a	n/a
7	ARID3A	chr5:37552742-37553918	K562	blood:	n/a	n/a
8	ARID3A	chr5:37717456-37718839	HepG2	liver:	n/a	chr5:37718035-37718051
9	ARID3A	chr5:37668578-37669026	HepG2	liver:	n/a	n/a
10	ARID3A	chr5:37723042-37723269	HepG2	liver:	n/a	n/a
11	ARID3A	chr5:37555087-37555396	K562	blood:	n/a	n/a
12	ARID3A	chr5:37723622-37723741	HepG2	liver:	n/a	n/a
13	ARID3A	chr5:37725466-37725597	HepG2	liver:	n/a	n/a
14	ATF1	chr5:37723031-37723344	K562	blood:	n/a	n/a
15	ATF1	chr5:37668620-37669142	K562	blood:	n/a	n/a
16	ATF1	chr5:37552974-37553744	K562	blood:	n/a	n/a
17	ATF1	chr5:37576224-37576625	K562	blood:	n/a	n/a
18	ATF1	chr5:37614336-37614416	K562	blood:	n/a	n/a
19	ATF1	chr5:37672268-37672700	K562	blood:	n/a	n/a
20	ATF2	chr5:37722807-37723371	GM12878	blood:	n/a	n/a
21	ATF2	chr5:37722812-37723380	GM12878	blood:	n/a	n/a
22	ATF2	chr5:37721531-37722125	GM12878	blood:	n/a	n/a
23	ATF2	chr5:37738072-37738628	GM12878	blood:	n/a	n/a
24	ATF2	chr5:37738148-37738641	GM12878	blood:	n/a	n/a
25	ATF2	chr5:37672199-37672626	GM12878	blood:	n/a	n/a
26	ATF3	chr5:37722947-37723383	K562	blood:	n/a	n/a
27	ATF3	chr5:37668562-37669111	HCT-116	colon:	n/a	n/a
28	ATF3	chr5:37668466-37669039	A549	lung:	n/a	n/a
29	ATF3	chr5:37668523-37668997	K562	blood:	n/a	n/a
30	ATF3	chr5:37668695-37668903	K562	blood:	n/a	n/a
31	ATF3	chr5:37668528-37669122	HCT-116	colon:	n/a	n/a
32	BACH1	chr5:37512136-37512171	K562	blood:	n/a	n/a
33	BACH1	chr5:37553100-37553687	K562	blood:	n/a	n/a
34	BACH1	chr5:37637658-37637891	H1-hESC	embryonic stem cell:	n/a	chr5:37637759-37637773
35	BATF	chr5:37738167-37738590	GM12878	blood:	n/a	n/a
36	BATF	chr5:37722967-37723392	GM12878	blood:	n/a	chr5:37723209-37723220
37	BATF	chr5:37721687-37721984	GM12878	blood:	n/a	chr5:37721867-37721878
38	BATF	chr5:37721677-37722017	GM12878	blood:	n/a	chr5:37721867-37721878
39	BATF	chr5:37711144-37711407	GM12878	blood:	n/a	chr5:37711278-37711289
40	BATF	chr5:37672308-37672700	GM12878	blood:	n/a	n/a
41	BATF	chr5:37672269-37672626	GM12878	blood:	n/a	n/a
42	BATF	chr5:37738147-37738489	GM12878	blood:	n/a	n/a
43	BATF	chr5:37723059-37723351	GM12878	blood:	n/a	chr5:37723209-37723220
44	BCL11A	chr5:37672314-37672635	GM12878	blood:	n/a	n/a
45	BCL11A	chr5:37722872-37723247	GM12878	blood:	n/a	n/a
46	BCL11A	chr5:37738167-37738447	GM12878	blood:	n/a	n/a
47	BCL11A	chr5:37738155-37738566	GM12878	blood:	n/a	n/a
48	BCL11A	chr5:37722940-37723281	GM12878	blood:	n/a	n/a
49	BCL3	chr5:37668388-37669097	A549	lung:	n/a	n/a
50	BCLAF1	chr5:37672321-37672667	GM12878	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37772265-37772315	HCF	heart:	n/a
2	chr5:37772265-37772315	HCF	heart:	n/a
3	chr5:37666865-37666915	HCT-116	colon:	n/a
4	chr5:37717768-37717818	Hepatocyte	liver:	n/a
5	chr5:37721782-37721832	HCM	heart:	n/a
6	chr5:37638144-37638194	HCF	heart:	n/a
7	chr5:37717768-37717818	ovcar-3	ovarian:	n/a
8	chr5:37723683-37723733	HEEpiC	esophagus:	n/a
9	chr5:37717768-37717818	PrEC	prostate:	n/a
10	chr5:37638144-37638194	SKMC	muscle:	n/a
11	chr5:37772265-37772315	Jurkat	blood:	n/a
12	chr5:37737626-37737676	MCF10A-Er-Src	breast:	n/a
13	chr5:37638144-37638194	BJ	skin:	n/a
14	chr5:37666865-37666915	HEEpiC	esophagus:	n/a
15	chr5:37723683-37723733	HMEC	breast:	n/a
16	chr5:37737626-37737676	Caco-2	colon:	n/a
17	chr5:37717768-37717818	AG09319	gingival:	n/a
18	chr5:37666865-37666915	Hela-S3	cervix:	n/a
19	chr5:37737626-37737676	MCF-7	breast:	n/a
20	chr5:37638144-37638194	HMEC	breast:	n/a
21	chr5:37717768-37717818	HRPEpiC	eye:	n/a
22	chr5:37737626-37737676	AG10803	skin:	n/a
23	chr5:37666865-37666915	HCM	heart:	n/a
24	chr5:37638144-37638194	HCT-116	colon:	n/a
25	chr5:37666865-37666915	HMEC	breast:	n/a
26	chr5:37772265-37772315	PANC-1	pancreas:	n/a
27	chr5:37721782-37721832	NHDF-neo	bronchial:	n/a
28	chr5:37721782-37721832	IMR90	lung:	fetal
29	chr5:37772265-37772315	SAEC	small airway:	n/a
30	chr5:37772265-37772315	NHBE	bronchial:	n/a
31	chr5:37717768-37717818	SKMC	muscle:	n/a
32	chr5:37721782-37721832	ProgFib	skin:	n/a
33	chr5:37717768-37717818	BJ	skin:	n/a
34	chr5:37721782-37721832	U87	brain:	n/a
35	chr5:37723683-37723733	Hepatocyte	liver:	n/a
36	chr5:37666865-37666915	RPTEC	kidney:	n/a
37	chr5:37721782-37721832	MCF10A-Er-Src	breast:	n/a
38	chr5:37772265-37772315	Hela-S3	cervix:	n/a
39	chr5:37721782-37721832	HEEpiC	esophagus:	n/a
40	chr5:37772265-37772315	HAEpiC	amniotic membrane:	n/a
41	chr5:37723683-37723733	ProgFib	skin:	n/a
42	chr5:37737626-37737676	ovcar-3	ovarian:	n/a
43	chr5:37666865-37666915	ECC-1	luminal epithelium:	n/a
44	chr5:37721782-37721832	AG04450	lung:	fetal
45	chr5:37666865-37666915	SAEC	small airway:	n/a
46	chr5:37717768-37717818	PFSK-1	brain:	n/a
47	chr5:37723683-37723733	AG04449	skin:	fetal
48	chr5:37737626-37737676	HCPEpiC	choroid plexus:	n/a
49	chr5:37772265-37772315	SKMC	muscle:	n/a
50	chr5:37638144-37638194	HRE	kidney:	n/a

(count:109 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:37477675..37480288-chr5:37486843..37489829,2	K562	blood:
2	chr5:37551824..37554603-chr5:37555317..37558093,4	K562	blood:
3	chr5:37541266..37543534-chr5:37545440..37547559,2	K562	blood:
4	chr5:37488881..37490858-chr5:37567347..37569058,2	K562	blood:
5	chr5:37708278..37710296-chr5:37714841..37716793,2	K562	blood:
6	chr5:37496762..37498368-chr5:37500019..37501730,2	MCF-7	breast:
7	chr5:37750239..37752814-chr5:37754556..37757334,3	K562	blood:
8	chr5:37702838..37705165-chr5:37705788..37708573,2	MCF-7	breast:
9	chr5:37583782..37585545-chr5:37586859..37589248,2	K562	blood:
10	chr5:37503334..37505446-chr5:37509179..37510910,2	K562	blood:
11	chr5:37628723..37630359-chr5:37632589..37634816,2	K562	blood:
12	chr5:37664491..37667181-chr5:37703176..37705396,2	MCF-7	breast:
13	chr5:37659630..37663695-chr5:37665450..37669812,5	K562	blood:
14	chr5:37565296..37570234-chr5:37571928..37578079,8	K562	blood:
15	chr5:37664491..37667181-chr5:37703176..37705396,2	MCF-7	breast:
16	chr5:37509914..37511896-chr5:37518755..37521412,2	K562	blood:
17	chr5:37553408..37554969-chr5:37565315..37567049,2	K562	blood:
18	chr5:37495029..37495917-chr5:37837475..37838072,2	MCF-7	breast:
19	chr5:37713205..37715908-chr5:37718081..37720863,2	K562	blood:
20	chr5:37572624..37574156-chr5:37580736..37583153,2	K562	blood:
21	chr5:37412783..37413436-chr5:37723453..37724202,2	K562	blood:
22	chr5:37495049..37495731-chr5:37758036..37758591,2	MCF-7	breast:
23	chr5:37750239..37752814-chr5:37754556..37757334,3	K562	blood:
24	chr5:37658934..37661849-chr5:37667178..37669216,3	MCF-7	breast:
25	chr5:37551924..37555267-chr5:37556271..37558320,3	K562	blood:
26	chr5:37574620..37576476-chr5:37584938..37587005,2	K562	blood:
27	chr5:37559780..37563110-chr5:37563759..37567373,3	K562	blood:
28	chr5:37630392..37632021-chr5:37637856..37640438,2	MCF-7	breast:
29	chr5:37713167..37714874-chr5:37723361..37725833,2	K562	blood:
30	chr5:37569124..37569718-chr8:118852447..118853416,2	MCF-7	breast:
31	chr5:37559780..37563110-chr5:37563759..37567373,3	K562	blood:
32	chr5:37728379..37730456-chr5:37761987..37763560,2	K562	blood:
33	chr5:37711423..37713283-chr5:37723723..37725531,2	K562	blood:
34	chr5:37550616..37553710-chr5:37559318..37562633,4	K562	blood:
35	chr5:37536707..37538331-chr5:37538401..37541156,2	K562	blood:
36	chr5:37662824..37665076-chr5:37668148..37670201,3	MCF-7	breast:
37	chr5:37766392..37770111-chr5:37772363..37774992,3	K562	blood:
38	chr5:37495049..37495731-chr5:37758036..37758591,2	MCF-7	breast:
39	chr5:37496762..37498368-chr5:37500019..37501730,2	MCF-7	breast:
40	chr5:37578232..37579991-chr5:37581584..37583169,2	MCF-7	breast:
41	chr5:37609718..37612103-chr5:37614733..37616548,2	K562	blood:
42	chr5:37412852..37413708-chr5:37554717..37555628,3	MCF-7	breast:
43	chr5:37551924..37555267-chr5:37556271..37558320,3	K562	blood:
44	chr5:37569701..37572288-chr5:37579867..37582083,2	MCF-7	breast:
45	chr5:37572624..37576201-chr5:37577602..37583153,5	K562	blood:
46	chr5:37378807..37379355-chr5:37554382..37555285,2	K562	blood:
47	chr5:37717152..37719759-chr5:37721474..37723768,2	K562	blood:
48	chr5:37503334..37505446-chr5:37509179..37510910,2	K562	blood:
49	chr5:37711775..37713303-chr5:37715445..37717839,2	K562	blood:
50	chr5:37565296..37570234-chr5:37571928..37578079,8	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUP155-5	chr5:37505790-37506959	NONHSAT101066

No data

Variant related genes	Relation type
RNU6-1190P	TF binding region
WDR70	TF binding region
ENSG00000248216	TF binding region
RNU6-484P	TF binding region
RNU6-1190P	CpG island
WDR70	CpG island
ENSG00000248216	CpG island
RNU6-484P	CpG island
ENSG00000082068	chromatin interactions
ENSG00000222743	chromatin interactions

Extended variants
information (count: 10442 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:10442 , 50 per page) page: 1 2 3 4 5 6 7 ... 209

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55862288	chr5:37485316-37485317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs571971265	chr5:37485341-37485342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs372590982	chr5:37485353-37485354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557482700	chr5:37485354-37485355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575963558	chr5:37485358-37485359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs34981953	chr5:37485360-37485361	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs555424461	chr5:37485393-37485394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554145388	chr5:37485422-37485423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573547309	chr5:37485453-37485454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs540830317	chr5:37485462-37485463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144822525	chr5:37485470-37485471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577534009	chr5:37485531-37485532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs9687741	chr5:37485532-37485533	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs556806719	chr5:37485575-37485576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs375514986	chr5:37485576-37485577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369949850	chr5:37485597-37485598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530922062	chr5:37485624-37485625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549253610	chr5:37485668-37485669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561362475	chr5:37485703-37485704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374288279	chr5:37485744-37485745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528545747	chr5:37485759-37485760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376635238	chr5:37485763-37485764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185852834	chr5:37485767-37485768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs367913868	chr5:37485790-37485791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372993405	chr5:37485791-37485792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571833095	chr5:37485839-37485840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189982981	chr5:37485876-37485877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs9716978	chr5:37485896-37485897	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs569583251	chr5:37485907-37485908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372567118	chr5:37485910-37485911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545286674	chr5:37485918-37485919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs142206798	chr5:37485919-37485920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559065858	chr5:37485921-37485922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555016423	chr5:37485943-37485944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs367859744	chr5:37485959-37485960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372187439	chr5:37485960-37485961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs57109943	chr5:37485976-37485977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs375458410	chr5:37486005-37486006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567032553	chr5:37486018-37486019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs9716982	chr5:37486036-37486037	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs552772986	chr5:37486059-37486060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181938631	chr5:37486060-37486061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545011642	chr5:37486061-37486062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557215196	chr5:37486092-37486093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575598756	chr5:37486115-37486116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs35426020	chr5:37486153-37486154	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs561553978	chr5:37486154-37486155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs141648758	chr5:37486165-37486166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543780735	chr5:37486179-37486180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528610853	chr5:37486219-37486220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
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
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
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	21346763	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	21990379	CNVD
Schizophrenia	19197363	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3361 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37463800-37489600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr5:37466000-37494400	Weak transcription	Osteobl	bone
3	chr5:37471600-37492400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr5:37476600-37513200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr5:37477000-37504400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr5:37478400-37502800	Weak transcription	Psoas Muscle	Psoas
7	chr5:37478600-37492800	Weak transcription	Stomach Mucosa	stomach
8	chr5:37478600-37494600	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr5:37478600-37502600	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr5:37479600-37486000	Weak transcription	HUVEC	blood vessel
11	chr5:37480400-37488000	Weak transcription	K562	blood
12	chr5:37480400-37488800	Weak transcription	Hela-S3	cervix
13	chr5:37480600-37493200	Weak transcription	HSMMtube	muscle
14	chr5:37480600-37493400	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr5:37480600-37495600	Weak transcription	HSMM	muscle
16	chr5:37480600-37510800	Weak transcription	Brain Angular Gyrus	brain
17	chr5:37480800-37486200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr5:37480800-37492400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr5:37480800-37493200	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr5:37481000-37489400	Weak transcription	Right Ventricle	heart
21	chr5:37481600-37487800	Weak transcription	A549	lung
22	chr5:37481600-37519200	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr5:37481800-37488000	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr5:37481800-37488000	Weak transcription	Fetal Lung	lung
25	chr5:37481800-37488400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr5:37481800-37489200	Weak transcription	Lung	lung
27	chr5:37481800-37489400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr5:37481800-37489400	Weak transcription	Esophagus	oesophagus
29	chr5:37481800-37490200	Weak transcription	Gastric	stomach
30	chr5:37481800-37492200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr5:37481800-37492400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr5:37481800-37493200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr5:37481800-37494600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr5:37481800-37494600	Weak transcription	Brain Hippocampus Middle	brain
35	chr5:37481800-37496800	Weak transcription	Aorta	Aorta
36	chr5:37481800-37499000	Weak transcription	HepG2	liver
37	chr5:37481800-37500400	Weak transcription	Brain Substantia Nigra	brain
38	chr5:37481800-37501400	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr5:37481800-37503200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr5:37481800-37503200	Weak transcription	Fetal Brain Male	brain
41	chr5:37481800-37507400	Weak transcription	Stomach Smooth Muscle	stomach
42	chr5:37481800-37519400	Weak transcription	Pancreas	Pancrea
43	chr5:37481800-37521200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr5:37482000-37487800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr5:37482000-37489200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr5:37482000-37492600	Weak transcription	Fetal Thymus	thymus
47	chr5:37482000-37500000	Weak transcription	Fetal Kidney	kidney
48	chr5:37482200-37486000	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr5:37482200-37487600	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr5:37482200-37487800	Weak transcription	Primary hematopoietic stem cells	blood

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