Variant report

Variant	nsv876817
Chromosome Location	chr3:56517253-56649282
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1395)
CpG islands
(count:613)
Chromatin interactive
region (count:33)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1395 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:56590851-56591380	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:56591601-56592288	K562	blood:	n/a	n/a
3	ARID3A	chr3:56528732-56529040	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:56591600-56592272	HepG2	liver:	n/a	n/a
5	ATF2	chr3:56591486-56591946	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr3:56528653-56529079	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr3:56590824-56591220	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr3:56528664-56529058	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr3:56528592-56529038	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr3:56536838-56537072	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr3:56522749-56523232	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr3:56645287-56645418	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr3:56590933-56590950	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr3:56592328-56592558	GM12878	blood:	n/a	n/a
15	BATF	chr3:56528719-56529051	GM12878	blood:	n/a	n/a
16	BCL11A	chr3:56528763-56528982	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCLAF1	chr3:56590884-56591283	GM12878	blood:	n/a	n/a
18	BCLAF1	chr3:56528680-56529098	GM12878	blood:	n/a	n/a
19	BHLHE40	chr3:56528733-56529063	GM12878	blood:	n/a	n/a
20	BHLHE40	chr3:56590983-56591813	K562	blood:	n/a	n/a
21	BHLHE40	chr3:56568281-56568481	K562	blood:	n/a	n/a
22	BHLHE40	chr3:56590970-56591312	GM12878	blood:	n/a	n/a
23	BHLHE40	chr3:56549037-56549546	HepG2	liver:	n/a	n/a
24	BRCA1	chr3:56591027-56591163	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr3:56590978-56591890	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr3:56559459-56559519	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr3:56528721-56529089	K562	blood:	n/a	n/a
28	CBX3	chr3:56528720-56529051	K562	blood:	n/a	n/a
29	CBX3	chr3:56590923-56591423	K562	blood:	n/a	n/a
30	CBX3	chr3:56591069-56591526	K562	blood:	n/a	n/a
31	CCNT2	chr3:56590957-56591472	K562	blood:	n/a	n/a
32	CEBPB	chr3:56528853-56529021	K562	blood:	n/a	chr3:56528952-56528963 chr3:56528952-56528965 chr3:56528954-56528963
33	CEBPB	chr3:56562913-56563157	HepG2	liver:	n/a	chr3:56563061-56563072
34	CEBPB	chr3:56590587-56591851	K562	blood:	n/a	chr3:56591677-56591694
35	CEBPB	chr3:56528689-56529191	ECC-1	luminal epithelium:	n/a	chr3:56528952-56528963 chr3:56528952-56528965 chr3:56528954-56528963
36	CEBPB	chr3:56590910-56591868	IMR90	lung:	n/a	chr3:56591677-56591694
37	CEBPB	chr3:56590919-56591278	HepG2	liver:	n/a	n/a
38	CEBPB	chr3:56590930-56591239	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr3:56566802-56566973	IMR90	lung:	n/a	chr3:56566903-56566916
40	CEBPB	chr3:56602814-56603020	HepG2	liver:	n/a	n/a
41	CEBPB	chr3:56542316-56542589	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr3:56564795-56565047	K562	blood:	n/a	chr3:56564889-56564900
43	CEBPB	chr3:56528741-56529176	GM12878	blood:	n/a	chr3:56528952-56528963 chr3:56528952-56528965 chr3:56528954-56528963
44	CEBPB	chr3:56528735-56529117	K562	blood:	n/a	chr3:56528952-56528963 chr3:56528952-56528965 chr3:56528954-56528963
45	CEBPB	chr3:56528751-56529252	MCF-7	breast:	n/a	chr3:56528952-56528963 chr3:56528952-56528965 chr3:56528954-56528963
46	CEBPB	chr3:56542315-56542606	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr3:56528689-56529168	HepG2	liver:	n/a	chr3:56528952-56528963 chr3:56528952-56528965 chr3:56528954-56528963
48	CEBPB	chr3:56590685-56592055	Hela-S3	cervix:	n/a	chr3:56591677-56591694
49	CEBPB	chr3:56528725-56529191	A549	lung:	n/a	chr3:56528952-56528963 chr3:56528952-56528965 chr3:56528954-56528963
50	CEBPB	chr3:56528566-56529204	HCT-116	colon:	n/a	chr3:56528952-56528963 chr3:56528952-56528965 chr3:56528954-56528963

(count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:56591125-56591175	LNCaP	prostate:	n/a
2	chr3:56591097-56591147	HMEC	breast:	n/a
3	chr3:56591241-56591291	IMR90	lung:	fetal
4	chr3:56591125-56591175	LNCaP	prostate:	n/a
5	chr3:56591097-56591147	HMEC	breast:	n/a
6	chr3:56591241-56591291	IMR90	lung:	fetal
7	chr3:56591125-56591175	HRE	kidney:	n/a
8	chr3:56590940-56590990	HRPEpiC	eye:	n/a
9	chr3:56591717-56591767	ProgFib	skin:	n/a
10	chr3:56588801-56588851	U87	brain:	n/a
11	chr3:56590942-56590992	IMR90	lung:	fetal
12	chr3:56590734-56590784	U87	brain:	n/a
13	chr3:56588801-56588851	SK-N-SH_RA	brain:	n/a
14	chr3:56591717-56591767	HCM	heart:	n/a
15	chr3:56591717-56591767	HEEpiC	esophagus:	n/a
16	chr3:56591097-56591147	MCF10A-Er-Src	breast:	n/a
17	chr3:56591125-56591175	SAEC	small airway:	n/a
18	chr3:56591097-56591147	HUVEC	blood vessel:	n/a
19	chr3:56590942-56590992	ProgFib	skin:	n/a
20	chr3:56590940-56590990	PrEC	prostate:	n/a
21	chr3:56588801-56588851	NH-A	brain:	n/a
22	chr3:56590942-56590992	PFSK-1	brain:	n/a
23	chr3:56590734-56590784	HCF	heart:	n/a
24	chr3:56591717-56591767	GM12891	blood:	n/a
25	chr3:56591190-56591240	GM19239	blood:	n/a
26	chr3:56590734-56590784	ECC-1	luminal epithelium:	n/a
27	chr3:56590734-56590784	BE2_C	brain:	n/a
28	chr3:56591241-56591291	MCF-7	breast:	n/a
29	chr3:56591241-56591291	HEK293	kidney:	embryo
30	chr3:56591717-56591767	HRE	kidney:	n/a
31	chr3:56591717-56591767	H1-hESC	embryonic stem cell:	embryo
32	chr3:56591190-56591240	HRE	kidney:	n/a
33	chr3:56590734-56590784	PrEC	prostate:	n/a
34	chr3:56591045-56591095	AG04449	skin:	fetal
35	chr3:56590942-56590992	HCM	heart:	n/a
36	chr3:56591717-56591767	SK-N-MC	brain:	n/a
37	chr3:56591241-56591291	PrEC	prostate:	n/a
38	chr3:56590942-56590992	HL-60	blood:	n/a
39	chr3:56590734-56590784	SKMC	muscle:	n/a
40	chr3:56591717-56591767	HCPEpiC	choroid plexus:	n/a
41	chr3:56590734-56590784	AG09309	skin:	n/a
42	chr3:56591045-56591095	BE2_C	brain:	n/a
43	chr3:56591190-56591240	A549	lung:	n/a
44	chr3:56591045-56591095	SK-N-SH	brain:	n/a
45	chr3:56588801-56588851	HCF	heart:	n/a
46	chr3:56591097-56591147	IMR90	lung:	fetal
47	chr3:56590940-56590990	Hepatocyte	liver:	n/a
48	chr3:56590942-56590992	AG10803	skin:	n/a
49	chr3:56591125-56591175	SK-N-MC	brain:	n/a
50	chr3:56590940-56590990	AG04450	lung:	fetal

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:56515621..56518439-chr3:56527168..56528675,2	K562	blood:
2	chr3:56515621..56518439-chr3:56527168..56528675,2	K562	blood:
3	chr3:56529898..56532445-chr3:56586043..56587761,2	K562	blood:
4	chr3:56588808..56592620-chr3:56662133..56663692,3	K562	blood:
5	chr3:56529898..56532445-chr3:56586043..56587761,2	K562	blood:
6	chr3:56589586..56592975-chr3:56714350..56719200,6	K562	blood:
7	chr3:56572461..56575309-chr3:56590695..56592695,2	K562	blood:
8	chr3:56480674..56481598-chr3:56528399..56529268,2	MCF-7	breast:
9	chr3:56590931..56593644-chr3:56601004..56602846,2	K562	blood:
10	chr17:61042877..61045351-chr3:56589650..56591304,2	MCF-7	breast:
11	chr3:56595109..56597404-chr3:56602239..56604027,2	K562	blood:
12	chr3:56569030..56570634-chr3:56588357..56591686,3	K562	blood:
13	chr3:56583067..56585146-chr3:56589206..56592962,3	K562	blood:
14	chr3:56589716..56592620-chr3:56662133..56663652,2	K562	blood:
15	chr3:56647300..56648856-chr3:56648916..56651486,2	K562	blood:
16	chr3:56590586..56593245-chr3:56606060..56608727,2	K562	blood:
17	chr11:122932229..122934551-chr3:56588931..56590451,2	K562	blood:
18	chr3:56515393..56518439-chr3:56526592..56528675,3	K562	blood:
19	chr11:85375746..85376542-chr3:56590683..56591527,2	Hela-S3	cervix:
20	chr3:56554359..56555305-chr3:71591429..71592069,2	MCF-7	breast:
21	chr3:56589231..56591997-chr3:56715959..56718849,3	K562	blood:
22	chr3:56563161..56565156-chr3:56590643..56593162,2	K562	blood:
23	chr3:56590666..56591170-chr6:28953586..28954086,2	HCT-116	colon:
24	chr3:56480877..56481665-chr3:56581433..56582100,2	MCF-7	breast:
25	chr3:56583673..56586258-chr3:56588811..56591335,4	MCF-7	breast:
26	chr3:56515393..56518439-chr3:56526592..56528675,3	K562	blood:
27	chr3:56588153..56590621-chr3:56591371..56592977,2	K562	blood:
28	chr3:56556169..56557738-chr3:56562979..56565848,2	K562	blood:
29	chr3:56591141..56591731-chr7:66766903..66767777,2	Hela-S3	cervix:
30	chr11:122932397..122933206-chr3:56588931..56589451,5	HCT-116	colon:
31	chr3:56595109..56597404-chr3:56602239..56604027,2	K562	blood:
32	chr3:56556169..56557738-chr3:56562979..56565848,2	K562	blood:
33	chr3:56619803..56621869-chr3:56626645..56628418,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPATA12-5	chr3:56600979-56601081	NONHSAT090055
2	lnc-SPATA12-5	chr3:56597544-56598153	NONHSAT090052
3	lnc-SPATA12-5	chr3:56605209-56605330	NONHSAT090053
4	lnc-SPATA12-5	chr3:56594890-56595250	NONHSAT090051
5	lnc-SPATA12-5	chr3:56600689-56600787	NONHSAT090053
6	lnc-SPATA12-5	chr3:56605209-56605330	NONHSAT090054
7	lnc-SPATA12-5	chr3:56600978-56601081	NONHSAT090053
8	lnc-SPATA12-5	chr3:56626998-56627089	NONHSAT090054
9	lnc-SPATA12-5	chr3:56600811-56601081	NONHSAT090054
10	lnc-SPATA12-5	chr3:56606365-56606938	NONHSAT090053
11	lnc-SPATA12-5	chr3:56592883-56592938	NONHSAT090051
12	lnc-SPATA12-5	chr3:56593597-56593622	NONHSAT090051
13	lnc-SPATA12-5	chr3:56605209-56605407	NONHSAT090055
14	lnc-SPATA12-5	chr3:56606365-56606456	NONHSAT090054
15	lnc-SPATA12-5	chr3:56599162-56599205	NONHSAT090052

No data

Variant related genes	Relation type
CCDC66	TF binding region
CCDC66	CpG island
ENSG00000163946	chromatin interactions
ENSG00000106610	chromatin interactions
ENSG00000180376	chromatin interactions
ENSG00000109971	chromatin interactions
ENSG00000227214	chromatin interactions
ENSG00000067601	chromatin interactions
ENSG00000263931	chromatin interactions
ENSG00000137504	chromatin interactions

Extended variants
information (count: 3601 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3601 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116442057	chr3:56521423-56521424	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs147605997	chr3:56521446-56521447	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs549704553	chr3:56521491-56521492	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs569871522	chr3:56521508-56521509	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs531696005	chr3:56521532-56521533	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs551933433	chr3:56521563-56521564	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs72877214	chr3:56521568-56521569	Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs142155536	chr3:56521633-56521634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs191058542	chr3:56521705-56521706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567861582	chr3:56521715-56521716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs536993193	chr3:56521727-56521728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556465667	chr3:56521730-56521731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs543833748	chr3:56521781-56521782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs112209311	chr3:56521816-56521817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576607596	chr3:56521819-56521820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545222113	chr3:56521826-56521827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557213298	chr3:56521827-56521828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558197496	chr3:56521832-56521833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs144443459	chr3:56521873-56521874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs540575181	chr3:56521917-56521918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs145507209	chr3:56521970-56521971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs2873348	chr3:56521972-56521973	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs543731624	chr3:56522000-56522001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs563316141	chr3:56522001-56522002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs112947504	chr3:56522010-56522011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552415406	chr3:56522098-56522099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571728611	chr3:56522101-56522102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545347970	chr3:56522102-56522103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs527836130	chr3:56522142-56522143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs75556880	chr3:56522146-56522147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567686213	chr3:56522168-56522169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs183252861	chr3:56522172-56522173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs556791082	chr3:56522173-56522174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs34815744	chr3:56522183-56522184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560380511	chr3:56522226-56522227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs570271426	chr3:56522231-56522232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs538809993	chr3:56522249-56522250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs573900389	chr3:56522278-56522279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs143420674	chr3:56522283-56522284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs187935938	chr3:56522305-56522306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs147987129	chr3:56522358-56522359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs28512349	chr3:56522373-56522374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs554249096	chr3:56522374-56522375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574401333	chr3:56522401-56522402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543072072	chr3:56522490-56522491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377640777	chr3:56522494-56522495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564433800	chr3:56522524-56522525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532312949	chr3:56522538-56522539	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546017932	chr3:56522559-56522560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561438925	chr3:56522601-56522602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	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
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Renal cell carcinoma	18765545	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:2141 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:56521400-56521600	Bivalent Enhancer	Fetal Muscle Leg	muscle
2	chr3:56521400-56521600	Enhancers	Fetal Stomach	stomach
3	chr3:56521600-56522800	Enhancers	Fetal Muscle Leg	muscle
4	chr3:56522400-56523400	Weak transcription	Fetal Stomach	stomach
5	chr3:56523200-56523400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr3:56523400-56524200	Enhancers	Fetal Stomach	stomach
7	chr3:56524200-56524400	Enhancers	Fetal Muscle Leg	muscle
8	chr3:56524600-56525000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr3:56525200-56525800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr3:56529000-56529200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
11	chr3:56529800-56530000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:56529800-56531000	Enhancers	HepG2	liver
13	chr3:56530000-56530400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:56530400-56531000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr3:56554200-56554800	Enhancers	Fetal Brain Male	brain
16	chr3:56554800-56556000	Weak transcription	Fetal Brain Male	brain
17	chr3:56556200-56556400	Enhancers	Fetal Brain Male	brain
18	chr3:56556400-56556600	Enhancers	H1 Cell Line	embryonic stem cell
19	chr3:56556400-56556600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr3:56556600-56560800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr3:56556800-56560800	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr3:56559400-56559600	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr3:56559400-56560000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr3:56559400-56561200	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr3:56559400-56561400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr3:56559600-56560600	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr3:56560000-56561000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr3:56560200-56561200	Enhancers	Brain Germinal Matrix	brain
29	chr3:56560400-56561000	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr3:56560400-56561000	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr3:56560400-56561200	Enhancers	H9 Cell Line	embryonic stem cell
32	chr3:56560400-56561200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr3:56560400-56561200	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr3:56560600-56561200	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr3:56560600-56561200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr3:56560800-56561200	Enhancers	H1 Cell Line	embryonic stem cell
37	chr3:56560800-56561400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr3:56561000-56561200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr3:56561200-56563400	Weak transcription	Brain Germinal Matrix	brain
40	chr3:56562200-56563000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr3:56563400-56566000	Enhancers	Brain Germinal Matrix	brain
42	chr3:56565000-56565200	Enhancers	Fetal Brain Female	brain
43	chr3:56565400-56566600	Weak transcription	Fetal Brain Female	brain
44	chr3:56566600-56567000	Enhancers	Fetal Brain Female	brain
45	chr3:56570400-56571200	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr3:56570800-56571200	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr3:56587200-56587400	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
48	chr3:56590000-56590400	Enhancers	HepG2	liver
49	chr3:56590000-56592000	Active TSS	NHDF-Ad	bronchial
50	chr3:56590200-56590400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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