Variant report

Variant	esv2753217
Chromosome Location	chr2:187424494-187470494
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1308)
CpG islands
(count:977)
Chromatin interactive
region (count:59)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1308 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:187457057-187457358	K562	blood:	n/a	n/a
2	ARID3A	chr2:187453822-187455000	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:187458734-187458821	K562	blood:	n/a	n/a
4	ARID3A	chr2:187433395-187433608	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:187435476-187435712	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:187435446-187435766	K562	blood:	n/a	n/a
7	ARID3A	chr2:187439988-187440337	K562	blood:	n/a	n/a
8	ARID3A	chr2:187455308-187455463	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:187459831-187460249	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:187440116-187440425	HepG2	liver:	n/a	n/a
11	ARID3A	chr2:187455669-187455948	HepG2	liver:	n/a	n/a
12	ARID3A	chr2:187454204-187454949	K562	blood:	n/a	n/a
13	ARID3A	chr2:187460039-187460181	K562	blood:	n/a	n/a
14	ARID3A	chr2:187455413-187456439	K562	blood:	n/a	n/a
15	ATF1	chr2:187448429-187448519	K562	blood:	n/a	n/a
16	ATF1	chr2:187457248-187457496	K562	blood:	n/a	n/a
17	ATF1	chr2:187440091-187440380	K562	blood:	n/a	n/a
18	ATF1	chr2:187455439-187456452	K562	blood:	n/a	n/a
19	ATF2	chr2:187454327-187455096	GM12878	blood:	n/a	n/a
20	ATF2	chr2:187455592-187456193	GM12878	blood:	n/a	n/a
21	ATF2	chr2:187455606-187456121	GM12878	blood:	n/a	n/a
22	ATF3	chr2:187437336-187437825	A549	lung:	n/a	n/a
23	ATF3	chr2:187455591-187456251	K562	blood:	n/a	chr2:187456091-187456104
24	ATF3	chr2:187437337-187437912	A549	lung:	n/a	n/a
25	ATF3	chr2:187439981-187440385	K562	blood:	n/a	n/a
26	ATF3	chr2:187435281-187435823	A549	lung:	n/a	n/a
27	ATF3	chr2:187454457-187455018	A549	lung:	n/a	chr2:187454494-187454503 chr2:187454488-187454497 chr2:187454853-187454862
28	ATF3	chr2:187440042-187440463	A549	lung:	n/a	n/a
29	ATF3	chr2:187440034-187440499	A549	lung:	n/a	n/a
30	BACH1	chr2:187440191-187440429	H1-hESC	embryonic stem cell:	n/a	chr2:187440259-187440273
31	BACH1	chr2:187460264-187460377	K562	blood:	n/a	n/a
32	BACH1	chr2:187454279-187455557	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr2:187440095-187440379	K562	blood:	n/a	chr2:187440259-187440273
34	BCL3	chr2:187439771-187440588	A549	lung:	n/a	n/a
35	BCL3	chr2:187437319-187437942	A549	lung:	n/a	n/a
36	BCL3	chr2:187437330-187438000	A549	lung:	n/a	n/a
37	BCL3	chr2:187454079-187454806	A549	lung:	n/a	chr2:187454493-187454502 chr2:187454488-187454501 chr2:187454494-187454507 chr2:187454741-187454750
38	BCL3	chr2:187435240-187435917	A549	lung:	n/a	n/a
39	BCL3	chr2:187454178-187454855	A549	lung:	n/a	chr2:187454493-187454502 chr2:187454488-187454501 chr2:187454494-187454507 chr2:187454810-187454819 chr2:187454741-187454750
40	BCLAF1	chr2:187454331-187455179	GM12878	blood:	n/a	chr2:187454493-187454502 chr2:187455010-187455019 chr2:187454488-187454501 chr2:187454494-187454507 chr2:187454810-187454819 chr2:187454741-187454750
41	BCLAF1	chr2:187454202-187455109	GM12878	blood:	n/a	chr2:187454493-187454502 chr2:187455010-187455019 chr2:187454488-187454501 chr2:187454494-187454507 chr2:187454810-187454819 chr2:187454741-187454750
42	BHLHE40	chr2:187455259-187455403	GM12878	blood:	n/a	n/a
43	BHLHE40	chr2:187453816-187456219	K562	blood:	n/a	chr2:187454843-187454859 chr2:187454565-187454581
44	BHLHE40	chr2:187459323-187459328	K562	blood:	n/a	n/a
45	BHLHE40	chr2:187454355-187454931	GM12878	blood:	n/a	chr2:187454843-187454859 chr2:187454565-187454581
46	BRCA1	chr2:187454490-187454930	HepG2	liver:	n/a	n/a
47	BRCA1	chr2:187454402-187454601	GM12878	blood:	n/a	n/a
48	BRCA1	chr2:187440976-187441206	Hela-S3	cervix:	n/a	n/a
49	CBX3	chr2:187440026-187440439	K562	blood:	n/a	n/a
50	CBX3	chr2:187454217-187454973	K562	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:187464581-187464631	HCM	heart:	n/a
2	chr2:187464581-187464631	HCM	heart:	n/a
3	chr2:187455488-187455538	BJ	skin:	n/a
4	chr2:187454613-187454663	Hepatocyte	liver:	n/a
5	chr2:187451704-187451754	HIPEpiC	eye:	n/a
6	chr2:187454414-187454464	NB4	blood:	n/a
7	chr2:187458732-187458782	LNCaP	prostate:	n/a
8	chr2:187454414-187454464	HCF	heart:	n/a
9	chr2:187454551-187454601	PANC-1	pancreas:	n/a
10	chr2:187464902-187464952	IMR90	lung:	fetal
11	chr2:187464581-187464631	HCT-116	colon:	n/a
12	chr2:187455488-187455538	LNCaP	prostate:	n/a
13	chr2:187454414-187454464	SK-N-MC	brain:	n/a
14	chr2:187464902-187464952	SAEC	small airway:	n/a
15	chr2:187464581-187464631	HCF	heart:	n/a
16	chr2:187455298-187455348	PANC-1	pancreas:	n/a
17	chr2:187464068-187464118	ovcar-3	ovarian:	n/a
18	chr2:187454613-187454663	HCF	heart:	n/a
19	chr2:187464068-187464118	Caco-2	colon:	n/a
20	chr2:187454299-187454349	HCT-116	colon:	n/a
21	chr2:187464902-187464952	HUVEC	blood vessel:	n/a
22	chr2:187454613-187454663	Caco-2	colon:	n/a
23	chr2:187464902-187464952	MCF-7	breast:	n/a
24	chr2:187454299-187454349	BJ	skin:	n/a
25	chr2:187464068-187464118	BJ	skin:	n/a
26	chr2:187454590-187454640	HIPEpiC	eye:	n/a
27	chr2:187455488-187455538	AG10803	skin:	n/a
28	chr2:187455488-187455538	Caco-2	colon:	n/a
29	chr2:187454551-187454601	GM19239	blood:	n/a
30	chr2:187454299-187454349	HPAEpiC	pulmonary alveolar:	n/a
31	chr2:187454414-187454464	HCT-116	colon:	n/a
32	chr2:187454299-187454349	HEK293	kidney:	embryo
33	chr2:187458732-187458782	AG10803	skin:	n/a
34	chr2:187464581-187464631	A549	lung:	n/a
35	chr2:187464902-187464952	RPTEC	kidney:	n/a
36	chr2:187454613-187454663	GM12891	blood:	n/a
37	chr2:187454259-187454309	HAEpiC	amniotic membrane:	n/a
38	chr2:187454747-187454797	HCPEpiC	choroid plexus:	n/a
39	chr2:187454613-187454663	T-47D	breast:	n/a
40	chr2:187454747-187454797	MCF10A-Er-Src	breast:	n/a
41	chr2:187451704-187451754	HCPEpiC	choroid plexus:	n/a
42	chr2:187458732-187458782	U87	brain:	n/a
43	chr2:187454590-187454640	BE2_C	brain:	n/a
44	chr2:187454551-187454601	MCF10A-Er-Src	breast:	n/a
45	chr2:187455298-187455348	MCF-7	breast:	n/a
46	chr2:187454414-187454464	BJ	skin:	n/a
47	chr2:187454414-187454464	NH-A	brain:	n/a
48	chr2:187454551-187454601	Caco-2	colon:	n/a
49	chr2:187464068-187464118	HNPCEpiC	eye:	n/a
50	chr2:187464068-187464118	ECC-1	luminal epithelium:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:187465660..187469278-chr2:187474543..187476426,3	K562	blood:
2	chr2:187352327..187355103-chr2:187460869..187462881,2	K562	blood:
3	chr2:187349672..187352615-chr2:187454696..187458504,4	K562	blood:
4	chr2:187406154..187410015-chr2:187435632..187441776,6	MCF-7	breast:
5	chr2:187470424..187473004-chr2:187473894..187476819,4	K562	blood:
6	chr2:187350070..187352270-chr2:187452591..187455868,3	MCF-7	breast:
7	chr11:75273135..75273713-chr2:187454417..187455033,2	Hela-S3	cervix:
8	chr2:187360313..187361827-chr2:187456108..187458564,2	K562	blood:
9	chr2:187459735..187462088-chr2:187466877..187468680,2	MCF-7	breast:
10	chr2:183901739..183903655-chr2:187454012..187455892,2	MCF-7	breast:
11	chr2:187349509..187352093-chr2:187424097..187426856,2	MCF-7	breast:
12	chr2:187459735..187462088-chr2:187466877..187468680,2	MCF-7	breast:
13	chr2:187350028..187353171-chr2:187452977..187457092,6	MCF-7	breast:
14	chr2:187414378..187416859-chr2:187424448..187427803,3	K562	blood:
15	chr2:187407559..187410721-chr2:187423895..187426771,4	MCF-7	breast:
16	chr2:187349171..187351570-chr2:187457346..187459477,2	MCF-7	breast:
17	chr2:187432930..187434820-chr2:187437011..187439461,2	MCF-7	breast:
18	chr2:187420574..187422329-chr2:187424400..187426246,2	K562	blood:
19	chr2:187466949..187471073-chr2:187471987..187477288,6	MCF-7	breast:
20	chr2:187359427..187362374-chr2:187449290..187451810,2	K562	blood:
21	chr2:187470425..187472217-chr2:187482022..187483885,2	MCF-7	breast:
22	chr2:187433275..187435459-chr2:187454415..187456337,2	MCF-7	breast:
23	chr2:187438759..187442258-chr2:187444014..187446139,4	MCF-7	breast:
24	chr2:187348960..187352767-chr2:187423783..187427050,3	K562	blood:
25	chr2:187437479..187442784-chr2:187443924..187447436,6	MCF-7	breast:
26	chr2:187418262..187420744-chr2:187454965..187457537,2	MCF-7	breast:
27	chr2:187451176..187453820-chr2:187556844..187559816,2	K562	blood:
28	chr2:187442776..187446488-chr2:187447901..187451766,4	MCF-7	breast:
29	chr2:187438412..187440075-chr2:187442178..187444992,2	K562	blood:
30	chr2:187370870..187374778-chr2:187436583..187438876,3	MCF-7	breast:
31	chr2:187350319..187353074-chr2:187452754..187457832,8	K562	blood:
32	chr2:187442776..187446488-chr2:187447901..187451766,4	MCF-7	breast:
33	chr2:187435611..187437376-chr2:187439116..187441984,2	MCF-7	breast:
34	chr2:187350920..187353075-chr2:187470374..187472407,2	K562	blood:
35	chr2:187411689..187413817-chr2:187434858..187437606,2	MCF-7	breast:
36	chr2:187432930..187434820-chr2:187437011..187439461,2	MCF-7	breast:
37	chr2:187350081..187352556-chr2:187433116..187434911,2	MCF-7	breast:
38	chr2:187406067..187412442-chr2:187438004..187442761,8	MCF-7	breast:
39	chr2:187435611..187437376-chr2:187439116..187441984,2	MCF-7	breast:
40	chr2:187396369..187398023-chr2:187440810..187442748,2	MCF-7	breast:
41	chr2:187438759..187442258-chr2:187444014..187446139,4	MCF-7	breast:
42	chr2:187435550..187437375-chr2:187442844..187445371,2	K562	blood:
43	chr2:187368789..187369555-chr2:187454140..187454681,2	MCF-7	breast:
44	chr2:187370485..187373217-chr2:187453776..187456177,3	MCF-7	breast:
45	chr2:187458884..187460611-chr2:187482455..187484231,2	K562	blood:
46	chr2:187435550..187437375-chr2:187442844..187445371,2	K562	blood:
47	chr2:187438845..187441409-chr2:187470852..187472926,2	K562	blood:
48	chr2:187465200..187467213-chr2:187503920..187506563,2	K562	blood:
49	chr2:187470424..187473004-chr2:187473894..187475620,2	K562	blood:
50	chr2:187370609..187373386-chr2:187454442..187456199,2	MCF-7	breast:

No data

Variant related genes	Relation type
ITGAV	TF binding region
ITGAV	CpG island
ENSG00000144369	chromatin interactions
ENSG00000138448	chromatin interactions
ENSG00000149257	chromatin interactions
ENSG00000224323	chromatin interactions
ENSG00000213953	chromatin interactions
ENSG00000227227	chromatin interactions
ENSG00000065548	chromatin interactions
ENSG00000061676	chromatin interactions

Extended variants
information (count: 1592 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:1592 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1375124	chr2:187424544-187424545	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544401576	chr2:187424552-187424553	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs562506788	chr2:187424566-187424567	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs533143926	chr2:187424680-187424681	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs144325599	chr2:187424682-187424683	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs10181681	chr2:187424711-187424712	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs148762814	chr2:187424715-187424716	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs79997959	chr2:187424783-187424784	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs533888575	chr2:187424784-187424785	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs185496866	chr2:187424801-187424802	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs537516170	chr2:187424807-187424808	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs556733733	chr2:187424872-187424873	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs571783400	chr2:187424901-187424902	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs375370035	chr2:187424948-187424949	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs544948381	chr2:187424950-187424951	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs572398229	chr2:187425037-187425038	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs6753278	chr2:187425077-187425078	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs554623068	chr2:187425118-187425119	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs576493414	chr2:187425152-187425153	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs150770474	chr2:187425189-187425190	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs201966415	chr2:187425190-187425191	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs572248963	chr2:187425191-187425192	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs6724486	chr2:187425192-187425193	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs189117964	chr2:187425287-187425288	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs533206738	chr2:187425310-187425311	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs192847197	chr2:187425351-187425352	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs149362337	chr2:187425434-187425435	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs560467752	chr2:187425469-187425470	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs72901398	chr2:187425500-187425501	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs76439429	chr2:187425502-187425503	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs143813047	chr2:187425518-187425519	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs567117827	chr2:187425522-187425523	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs184342381	chr2:187425582-187425583	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs79505622	chr2:187425726-187425727	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs571008562	chr2:187425756-187425757	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs538888376	chr2:187425809-187425810	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs188383382	chr2:187425832-187425833	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs36011939	chr2:187425915-187425916	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs181159219	chr2:187425992-187425993	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs139865606	chr2:187426002-187426003	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs555225877	chr2:187426004-187426005	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs184146751	chr2:187426018-187426019	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs79609497	chr2:187426079-187426080	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs189075438	chr2:187426098-187426099	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs143160650	chr2:187426115-187426116	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs181021142	chr2:187426116-187426117	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs556508472	chr2:187426174-187426175	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs572385538	chr2:187426236-187426237	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs151152828	chr2:187426251-187426252	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs561214943	chr2:187426373-187426374	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:49)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Urothelial carcinoma	21177765	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1417 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:187414400-187426400	Weak transcription	Aorta	Aorta
2	chr2:187420000-187426000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr2:187420200-187434800	Weak transcription	NHEK	skin
4	chr2:187420800-187426200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:187423000-187426600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr2:187423600-187424800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr2:187423800-187425600	Enhancers	GM12878-XiMat	blood
8	chr2:187423800-187426200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr2:187423800-187426200	Weak transcription	A549	lung
10	chr2:187424800-187425000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr2:187424800-187425000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr2:187425000-187426400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr2:187425000-187426400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr2:187425200-187426200	Weak transcription	HUVEC	blood vessel
15	chr2:187425800-187426200	Enhancers	HepG2	liver
16	chr2:187426000-187426400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr2:187426000-187426600	Enhancers	Placenta Amnion	Placenta Amnion
18	chr2:187426200-187426400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr2:187426200-187426600	Enhancers	A549	lung
20	chr2:187426200-187426800	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr2:187426200-187426800	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr2:187426200-187426800	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr2:187426200-187426800	Flanking Active TSS	HepG2	liver
24	chr2:187426200-187426800	Enhancers	K562	blood
25	chr2:187426200-187427000	Enhancers	HUVEC	blood vessel
26	chr2:187426200-187427400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr2:187426400-187426600	Enhancers	Aorta	Aorta
28	chr2:187426400-187426800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr2:187426400-187426800	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr2:187426400-187426800	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr2:187426400-187426800	Enhancers	HMEC	breast
32	chr2:187426400-187427000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr2:187426400-187427600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr2:187426600-187441200	Weak transcription	Aorta	Aorta
35	chr2:187426800-187427000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr2:187426800-187427200	Enhancers	HepG2	liver
37	chr2:187427200-187429000	Weak transcription	HepG2	liver
38	chr2:187431000-187433600	Weak transcription	HepG2	liver
39	chr2:187433400-187434400	Weak transcription	A549	lung
40	chr2:187433600-187434600	Enhancers	HepG2	liver
41	chr2:187434400-187434600	Enhancers	A549	lung
42	chr2:187434400-187436200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr2:187434600-187434800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr2:187434600-187435000	Flanking Active TSS	HepG2	liver
45	chr2:187434600-187435200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr2:187434600-187435400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr2:187434600-187435400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr2:187434600-187435400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr2:187434600-187435600	Enhancers	H1 Cell Line	embryonic stem cell
50	chr2:187434600-187435800	Enhancers	ES-I3 Cell Line	embryonic stem cell

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