Variant report

Variant	nsv876746
Chromosome Location	chr3:46778988-46831775
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	ATF3	chr3:46792267-46792609	K562	blood:	n/a	n/a
2	ATF3	chr3:46792308-46792631	K562	blood:	n/a	n/a
3	BHLHE40	chr3:46792161-46792741	K562	blood:	n/a	chr3:46792470-46792479 chr3:46792470-46792479
4	BHLHE40	chr3:46798309-46798511	K562	blood:	n/a	n/a
5	CBX3	chr3:46792069-46792673	K562	blood:	n/a	n/a
6	CBX3	chr3:46805384-46805615	K562	blood:	n/a	n/a
7	CBX3	chr3:46798157-46798548	K562	blood:	n/a	n/a
8	CCNT2	chr3:46792259-46792508	K562	blood:	n/a	n/a
9	CEBPB	chr3:46780721-46781004	HepG2	liver:	n/a	n/a
10	CEBPB	chr3:46780720-46780724	Hela-S3	cervix:	n/a	n/a
11	CHD2	chr3:46798208-46798651	K562	blood:	n/a	n/a
12	CHD2	chr3:46798433-46798503	HepG2	liver:	n/a	n/a
13	CTCF	chr3:46792360-46792510	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792394-46792407
14	CTCF	chr3:46819600-46819750	GM12873	blood:	n/a	n/a
15	CTCF	chr3:46794616-46794658	GM19240	blood:	n/a	n/a
16	CTCF	chr3:46794180-46794330	GM12873	blood:	n/a	n/a
17	CTCF	chr3:46798300-46798450	HepG2	liver:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
18	CTCF	chr3:46794460-46794610	GM06990	blood:	n/a	n/a
19	CTCF	chr3:46798300-46798450	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
20	CTCF	chr3:46794500-46794650	GM12873	blood:	n/a	n/a
21	CTCF	chr3:46798354-46798408	Gliobla	brain:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
22	CTCF	chr3:46794500-46794650	GM12866	blood:	n/a	n/a
23	CTCF	chr3:46792209-46792538	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792234-46792247 chr3:46792394-46792407
24	CTCF	chr3:46801730-46801825	HUVEC	blood vessel:	n/a	n/a
25	CTCF	chr3:46794360-46794510	GM12873	blood:	n/a	n/a
26	CTCF	chr3:46794520-46794670	GM12864	blood:	n/a	n/a
27	CTCF	chr3:46792356-46792487	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792394-46792407
28	CTCF	chr3:46794460-46794610	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr3:46792287-46792555	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792394-46792407
30	CTCF	chr3:46798400-46798550	HVMF	connective:	n/a	n/a
31	CTCF	chr3:46798136-46798509	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
32	CTCF	chr3:46798156-46798539	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
33	CTCF	chr3:46798280-46798430	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
34	CTCF	chr3:46794500-46794650	GM12872	blood:	n/a	n/a
35	CTCF	chr3:46798359-46798450	LNCaP	prostate:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
36	CTCF	chr3:46798336-46798412	H1-hESC	embryonic stem cell:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
37	CTCF	chr3:46794560-46794710	HCT-116	colon:	n/a	n/a
38	CTCF	chr3:46792152-46792625	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792234-46792247 chr3:46792394-46792407
39	CTCF	chr3:46798280-46798435	HepG2	liver:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
40	CTCF	chr3:46798134-46798571	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
41	CTCF	chr3:46794600-46794750	GM12875	blood:	n/a	n/a
42	CTCF	chr3:46798034-46798529	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
43	CTCF	chr3:46797989-46798564	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
44	CTCFL	chr3:46792338-46792472	K562	blood:	n/a	n/a
45	CTCFL	chr3:46798305-46798476	K562	blood:	n/a	n/a
46	CTCFL	chr3:46798258-46798497	K562	blood:	n/a	n/a
47	CTCFL	chr3:46792291-46792513	K562	blood:	n/a	n/a
48	E2F4	chr3:46790087-46790145	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr3:46799519-46799724	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F6	chr3:46798276-46798526	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46792357-46792407	AG04449	skin:	fetal
2	chr3:46792357-46792407	AG04449	skin:	fetal
3	chr3:46798240-46798290	SKMC	muscle:	n/a
4	chr3:46797928-46797978	HRCEpiC	kidney:	n/a
5	chr3:46797928-46797978	HAEpiC	amniotic membrane:	n/a
6	chr3:46792023-46792073	HL-60	blood:	n/a
7	chr3:46792364-46792414	GM12892	blood:	n/a
8	chr3:46796026-46796076	Jurkat	blood:	n/a
9	chr3:46792462-46792512	PFSK-1	brain:	n/a
10	chr3:46786238-46786288	K562	blood:	n/a
11	chr3:46786387-46786437	A549	lung:	n/a
12	chr3:46792192-46792242	HCPEpiC	choroid plexus:	n/a
13	chr3:46799010-46799060	AG04450	lung:	fetal
14	chr3:46796026-46796076	ovcar-3	ovarian:	n/a
15	chr3:46792192-46792242	IMR90	lung:	fetal
16	chr3:46792462-46792512	NHDF-neo	bronchial:	n/a
17	chr3:46786387-46786437	ProgFib	skin:	n/a
18	chr3:46791477-46791527	HEEpiC	esophagus:	n/a
19	chr3:46792023-46792073	IMR90	lung:	fetal
20	chr3:46792023-46792073	AG09309	skin:	n/a
21	chr3:46798240-46798290	SAEC	small airway:	n/a
22	chr3:46792364-46792414	CMK	blood:	n/a
23	chr3:46792364-46792414	HL-60	blood:	n/a
24	chr3:46786387-46786437	AoSMC	blood vessel:	n/a
25	chr3:46787073-46787123	T-47D	breast:	n/a
26	chr3:46792023-46792073	HMEC	breast:	n/a
27	chr3:46801208-46801258	PANC-1	pancreas:	n/a
28	chr3:46797928-46797978	SK-N-MC	brain:	n/a
29	chr3:46801208-46801258	RPTEC	kidney:	n/a
30	chr3:46790182-46790232	T-47D	breast:	n/a
31	chr3:46796026-46796076	IMR90	lung:	fetal
32	chr3:46792462-46792512	HCPEpiC	choroid plexus:	n/a
33	chr3:46797928-46797978	HUVEC	blood vessel:	n/a
34	chr3:46792364-46792414	HEK293	kidney:	embryo
35	chr3:46799010-46799060	T-47D	breast:	n/a
36	chr3:46790182-46790232	BE2_C	brain:	n/a
37	chr3:46787073-46787123	HEK293	kidney:	embryo
38	chr3:46799010-46799060	SAEC	small airway:	n/a
39	chr3:46799010-46799060	A549	lung:	n/a
40	chr3:46792192-46792242	ovcar-3	ovarian:	n/a
41	chr3:46792462-46792512	HRPEpiC	eye:	n/a
42	chr3:46792357-46792407	H1-hESC	embryonic stem cell:	embryo
43	chr3:46790182-46790232	HepG2	liver:	n/a
44	chr3:46801208-46801258	NT2-D1	testis:	n/a
45	chr3:46792357-46792407	SK-N-SH	brain:	n/a
46	chr3:46797928-46797978	HRPEpiC	eye:	n/a
47	chr3:46789735-46789785	LNCaP	prostate:	n/a
48	chr3:46792364-46792414	SK-N-MC	brain:	n/a
49	chr3:46798240-46798290	NH-A	brain:	n/a
50	chr3:46799010-46799060	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:46746227..46747136-chr3:46797879..46798830,2	K562	blood:
2	chr3:46780314..46782174-chr3:46791450..46793098,2	K562	blood:
3	chr3:46789981..46792010-chr3:46794604..46797550,3	K562	blood:
4	chr3:46789741..46793223-chr3:46794604..46798425,5	K562	blood:
5	chr3:46780631..46782178-chr3:46786371..46787877,2	K562	blood:
6	chr3:46787160..46789838-chr3:46792836..46795181,2	K562	blood:
7	chr3:46764632..46767218-chr3:46782393..46785331,2	K562	blood:
8	chr3:46819637..46822469-chr3:46912934..46914923,2	K562	blood:
9	chr3:46774758..46775741-chr3:46797694..46798443,2	K562	blood:
10	chr3:46803507..46806312-chr3:46807817..46810409,2	K562	blood:
11	chr3:46787160..46789838-chr3:46792836..46795181,2	K562	blood:
12	chr3:46788120..46791042-chr3:46798895..46800766,2	K562	blood:
13	chr3:46776204..46778019-chr3:46778181..46780158,2	K562	blood:
14	chr3:46720178..46722487-chr3:46787613..46789601,2	K562	blood:
15	chr3:46789741..46793223-chr3:46794604..46798425,5	K562	blood:
16	chr3:46796974..46798578-chr3:46800470..46803376,2	K562	blood:
17	chr3:46783977..46786592-chr3:46791856..46793997,2	MCF-7	breast:
18	chr3:46796204..46798578-chr3:46800470..46803401,3	K562	blood:
19	chr3:46780314..46782174-chr3:46791450..46793098,2	K562	blood:
20	chr3:46796974..46798578-chr3:46800470..46803376,2	K562	blood:
21	chr3:46785802..46787615-chr3:46790135..46792444,2	K562	blood:
22	chr3:46796598..46799185-chr3:46799676..46801957,2	MCF-7	breast:
23	chr3:46796204..46798578-chr3:46800470..46803401,3	K562	blood:
24	chr3:46783774..46785518-chr3:46915413..46918248,2	MCF-7	breast:
25	chr3:46780631..46782178-chr3:46786371..46787877,2	K562	blood:
26	chr3:46792775..46794351-chr3:46906387..46908133,2	K562	blood:
27	chr3:46789981..46792010-chr3:46794604..46797550,3	K562	blood:
28	chr3:46803507..46806312-chr3:46807817..46810409,2	K562	blood:
29	chr3:46788120..46791042-chr3:46798895..46800766,2	K562	blood:
30	chr3:46798748..46799515-chr3:46907913..46908649,2	K562	blood:
31	chr3:46796598..46799185-chr3:46799676..46801957,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRSS50-1	chr3:46795974-46796138	NONHSAT089457
2	lnc-PRSS50-1	chr3:46797532-46798119	NONHSAT089457

Variant related genes	Relation type
PRSS45	TF binding region
PRSS46	TF binding region
PRSS45	CpG island
PRSS46	CpG island
ENSG00000188086	chromatin interactions
ENSG00000261603	chromatin interactions

Extended variants
information (count: 1061 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1061 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6763438	chr3:46778988-46778989	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535944554	chr3:46779054-46779055	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs35708476	chr3:46779109-46779110	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs180992711	chr3:46779113-46779114	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs59711990	chr3:46779114-46779115	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs569846501	chr3:46779186-46779187	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs6772081	chr3:46779187-46779188	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs149199405	chr3:46779192-46779193	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs145020563	chr3:46779224-46779225	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs576414420	chr3:46779228-46779229	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs148530966	chr3:46779237-46779238	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs372263019	chr3:46779271-46779272	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs574409054	chr3:46779286-46779287	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs531617920	chr3:46779357-46779358	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs541925160	chr3:46779391-46779392	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs6414431	chr3:46779410-46779411	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs531154941	chr3:46779413-46779414	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs6414432	chr3:46779431-46779432	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs564807952	chr3:46779433-46779434	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs528489293	chr3:46779446-46779447	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs113211508	chr3:46779503-46779504	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs546628302	chr3:46779504-46779505	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs534129001	chr3:46779506-46779507	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs6442025	chr3:46779547-46779548	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs529336868	chr3:46779573-46779574	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs551077323	chr3:46779584-46779585	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs6797059	chr3:46779654-46779655	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs62246229	chr3:46779689-46779690	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs557449798	chr3:46779733-46779734	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs558421087	chr3:46779765-46779766	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs6442026	chr3:46779799-46779800	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs185374875	chr3:46779832-46779833	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs6794689	chr3:46779846-46779847	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs574395090	chr3:46779847-46779848	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs541536499	chr3:46779864-46779865	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs557052560	chr3:46779875-46779876	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs553810419	chr3:46779876-46779877	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs370825424	chr3:46779880-46779881	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs142893812	chr3:46779908-46779909	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs546464302	chr3:46779924-46779925	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs6782136	chr3:46779955-46779956	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs573540205	chr3:46780003-46780004	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs540939489	chr3:46780033-46780034	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs561909319	chr3:46780041-46780042	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs11342997	chr3:46780070-46780071	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs386660753	chr3:46780071-46780072	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs200059636	chr3:46780072-46780073	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs151066377	chr3:46780215-46780216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs13075068	chr3:46780228-46780229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571481752	chr3:46780270-46780271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Recurrent pregnancy loss	19789632	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46744000-46792200	Weak transcription	Right Atrium	heart
2	chr3:46769000-46792400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr3:46777000-46779800	Enhancers	Thymus	Thymus
4	chr3:46778000-46780000	Enhancers	Fetal Thymus	thymus
5	chr3:46778400-46779200	Enhancers	Fetal Muscle Trunk	muscle
6	chr3:46778600-46779200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr3:46778600-46779200	Enhancers	Fetal Muscle Leg	muscle
8	chr3:46778800-46779000	Bivalent Enhancer	HSMM	muscle
9	chr3:46778800-46779200	Enhancers	Left Ventricle	heart
10	chr3:46778800-46779400	Enhancers	Pancreas	Pancrea
11	chr3:46779000-46779200	Enhancers	Spleen	Spleen
12	chr3:46779000-46779400	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
13	chr3:46779200-46782000	Weak transcription	Left Ventricle	heart
14	chr3:46779400-46795400	Weak transcription	Spleen	Spleen
15	chr3:46779400-46799600	Weak transcription	Pancreas	Pancrea
16	chr3:46779600-46780400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr3:46779800-46792800	Weak transcription	Thymus	Thymus
18	chr3:46780800-46785000	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr3:46784400-46785200	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr3:46784400-46785200	Enhancers	Fetal Stomach	stomach
21	chr3:46784600-46785000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr3:46784600-46785000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr3:46784600-46785000	Enhancers	Placenta	Placenta
24	chr3:46784600-46785200	Enhancers	Fetal Lung	lung
25	chr3:46784600-46785200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
26	chr3:46784800-46785200	Enhancers	Fetal Intestine Small	intestine
27	chr3:46785000-46785200	Weak transcription	Placenta	Placenta
28	chr3:46785000-46785800	Strong transcription	Skeletal Muscle Male	skeletal muscle
29	chr3:46785000-46786200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr3:46785000-46789800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr3:46785200-46785600	Enhancers	Placenta	Placenta
32	chr3:46785200-46799800	Weak transcription	Fetal Intestine Small	intestine
33	chr3:46785600-46789800	Weak transcription	Placenta	Placenta
34	chr3:46785800-46786200	Enhancers	GM12878-XiMat	blood
35	chr3:46785800-46795600	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr3:46786200-46787800	Weak transcription	GM12878-XiMat	blood
37	chr3:46786400-46786600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr3:46787800-46789200	Enhancers	GM12878-XiMat	blood
39	chr3:46789200-46794200	Weak transcription	GM12878-XiMat	blood
40	chr3:46789600-46789800	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr3:46789600-46790400	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr3:46789600-46790400	Enhancers	Fetal Muscle Leg	muscle
43	chr3:46789800-46790000	Enhancers	Fetal Stomach	stomach
44	chr3:46789800-46790200	Enhancers	H9 Cell Line	embryonic stem cell
45	chr3:46789800-46790400	Enhancers	Placenta	Placenta
46	chr3:46789800-46790600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr3:46790600-46791800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr3:46791800-46792400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr3:46792200-46792800	Flanking Bivalent TSS/Enh	K562	blood
50	chr3:46792400-46794200	Enhancers	Placenta Amnion	Placenta Amnion

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