Variant report

Variant	nsv1001461
Chromosome Location	chr2:78091352-78673948
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1347)
CpG islands
(count:306)
Chromatin interactive
region (count:30)
LncRNA
region (count:39)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1347 , 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	chr2:78643666-78644757	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:78336522-78336700	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:78361077-78361118	K562	blood:	n/a	n/a
4	ARID3A	chr2:78487915-78488675	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:78532952-78532953	K562	blood:	n/a	n/a
6	ARID3A	chr2:78578413-78578720	K562	blood:	n/a	n/a
7	ARID3A	chr2:78653375-78653864	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:78413821-78414186	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:78578391-78578636	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:78389314-78389802	HepG2	liver:	n/a	n/a
11	ATF1	chr2:78215207-78215394	K562	blood:	n/a	n/a
12	ATF1	chr2:78361002-78361126	K562	blood:	n/a	n/a
13	ATF1	chr2:78166529-78166714	K562	blood:	n/a	n/a
14	ATF1	chr2:78408127-78408325	K562	blood:	n/a	n/a
15	BACH1	chr2:78477710-78477711	K562	blood:	n/a	n/a
16	BACH1	chr2:78368178-78368199	K562	blood:	n/a	n/a
17	BATF	chr2:78508305-78508535	GM12878	blood:	n/a	n/a
18	BATF	chr2:78428253-78428380	GM12878	blood:	n/a	n/a
19	BATF	chr2:78508306-78508624	GM12878	blood:	n/a	n/a
20	BCL11A	chr2:78263040-78263247	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL11A	chr2:78508311-78508495	GM12878	blood:	n/a	n/a
22	BDP1	chr2:78181978-78182355	K562	blood:	n/a	n/a
23	BHLHE40	chr2:78487986-78488343	HepG2	liver:	n/a	n/a
24	BHLHE40	chr2:78389461-78389669	HepG2	liver:	n/a	n/a
25	BHLHE40	chr2:78490807-78490864	GM12878	blood:	n/a	n/a
26	BHLHE40	chr2:78189217-78189406	HepG2	liver:	n/a	n/a
27	BHLHE40	chr2:78508455-78508636	GM12878	blood:	n/a	n/a
28	CBX3	chr2:78256529-78256863	K562	blood:	n/a	n/a
29	CBX3	chr2:78256534-78256829	K562	blood:	n/a	n/a
30	CBX3	chr2:78182148-78182464	K562	blood:	n/a	n/a
31	CBX3	chr2:78182081-78182419	K562	blood:	n/a	n/a
32	CBX3	chr2:78273156-78273427	K562	blood:	n/a	n/a
33	CBX3	chr2:78273160-78273446	K562	blood:	n/a	n/a
34	CCNT2	chr2:78252676-78252871	K562	blood:	n/a	n/a
35	CCNT2	chr2:78110616-78110816	K562	blood:	n/a	n/a
36	CEBPB	chr2:78641606-78642279	HepG2	liver:	n/a	chr2:78641752-78641763
37	CEBPB	chr2:78369163-78369459	HepG2	liver:	n/a	chr2:78369346-78369359 chr2:78369367-78369378
38	CEBPB	chr2:78518603-78518888	A549	lung:	n/a	chr2:78518707-78518718
39	CEBPB	chr2:78389426-78389688	HepG2	liver:	n/a	n/a
40	CEBPB	chr2:78445231-78445483	H1-hESC	embryonic stem cell:	n/a	chr2:78445380-78445391
41	CEBPB	chr2:78560444-78560597	HepG2	liver:	n/a	chr2:78560467-78560478
42	CEBPB	chr2:78413736-78414060	A549	lung:	n/a	chr2:78413883-78413892 chr2:78413883-78413892 chr2:78413883-78413892 chr2:78413881-78413894 chr2:78413882-78413893 chr2:78413881-78413894 chr2:78413881-78413892 chr2:78413883-78413892
43	CEBPB	chr2:78162903-78163211	K562	blood:	n/a	chr2:78163175-78163186 chr2:78163032-78163043
44	CEBPB	chr2:78359289-78359640	MCF-7	breast:	n/a	n/a
45	CEBPB	chr2:78336390-78336918	HepG2	liver:	n/a	n/a
46	CEBPB	chr2:78640615-78640922	K562	blood:	n/a	chr2:78640779-78640790 chr2:78640781-78640790
47	CEBPB	chr2:78570869-78570882	K562	blood:	n/a	n/a
48	CEBPB	chr2:78204751-78204849	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr2:78336457-78336742	K562	blood:	n/a	n/a
50	CEBPB	chr2:78175125-78175449	IMR90	lung:	n/a	chr2:78175273-78175284 chr2:78175274-78175283 chr2:78175272-78175285 chr2:78175272-78175285 chr2:78175271-78175288 chr2:78175272-78175283

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:78182197-78182247	A549	lung:	n/a
2	chr2:78182197-78182247	A549	lung:	n/a
3	chr2:78182187-78182237	HRCEpiC	kidney:	n/a
4	chr2:78263008-78263058	HUVEC	blood vessel:	n/a
5	chr2:78182197-78182247	GM19239	blood:	n/a
6	chr2:78545567-78545617	Hepatocyte	liver:	n/a
7	chr2:78545567-78545617	AG09309	skin:	n/a
8	chr2:78263008-78263058	AG04450	lung:	fetal
9	chr2:78545567-78545617	GM12892	blood:	n/a
10	chr2:78545567-78545617	HCT-116	colon:	n/a
11	chr2:78182350-78182400	HCM	heart:	n/a
12	chr2:78182197-78182247	HMEC	breast:	n/a
13	chr2:78263008-78263058	NH-A	brain:	n/a
14	chr2:78182187-78182237	HCF	heart:	n/a
15	chr2:78182350-78182400	SK-N-MC	brain:	n/a
16	chr2:78545567-78545617	Jurkat	blood:	n/a
17	chr2:78182350-78182400	LNCaP	prostate:	n/a
18	chr2:78263008-78263058	HRE	kidney:	n/a
19	chr2:78545567-78545617	HL-60	blood:	n/a
20	chr2:78182350-78182400	AoSMC	blood vessel:	n/a
21	chr2:78182350-78182400	GM12892	blood:	n/a
22	chr2:78182350-78182400	Caco-2	colon:	n/a
23	chr2:78182187-78182237	Jurkat	blood:	n/a
24	chr2:78182187-78182237	GM12891	blood:	n/a
25	chr2:78182197-78182247	GM12878	blood:	n/a
26	chr2:78182350-78182400	HEEpiC	esophagus:	n/a
27	chr2:78182187-78182237	HMEC	breast:	n/a
28	chr2:78263008-78263058	HPAEpiC	pulmonary alveolar:	n/a
29	chr2:78545567-78545617	HRCEpiC	kidney:	n/a
30	chr2:78545567-78545617	CMK	blood:	n/a
31	chr2:78182197-78182247	U87	brain:	n/a
32	chr2:78182197-78182247	RPTEC	kidney:	n/a
33	chr2:78182197-78182247	HEEpiC	esophagus:	n/a
34	chr2:78182350-78182400	U87	brain:	n/a
35	chr2:78182350-78182400	HCT-116	colon:	n/a
36	chr2:78182187-78182237	Hela-S3	cervix:	n/a
37	chr2:78263008-78263058	GM12891	blood:	n/a
38	chr2:78182350-78182400	AG09319	gingival:	n/a
39	chr2:78182187-78182237	BE2_C	brain:	n/a
40	chr2:78182197-78182247	NHBE	bronchial:	n/a
41	chr2:78263008-78263058	U87	brain:	n/a
42	chr2:78182197-78182247	SK-N-SH	brain:	n/a
43	chr2:78182350-78182400	GM12891	blood:	n/a
44	chr2:78182187-78182237	GM12878	blood:	n/a
45	chr2:78182197-78182247	PFSK-1	brain:	n/a
46	chr2:78545567-78545617	SAEC	small airway:	n/a
47	chr2:78182197-78182247	GM12891	blood:	n/a
48	chr2:78182197-78182247	NHDF-neo	bronchial:	n/a
49	chr2:78263008-78263058	IMR90	lung:	fetal
50	chr2:78182350-78182400	AG10803	skin:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:78577613..78578539-chr2:79206466..79207847,3	MCF-7	breast:
2	chr2:78326493..78328202-chr2:78333273..78335963,2	K562	blood:
3	chr2:78607954..78609567-chr2:78764622..78766807,2	K562	blood:
4	chr2:78295743..78297764-chr2:78300068..78303067,2	K562	blood:
5	chr2:78300847..78302731-chr2:78308537..78310502,2	K562	blood:
6	chr2:78347733..78349406-chr2:78351881..78353903,2	K562	blood:
7	chr2:78578903..78584135-chr2:78585848..78590226,6	K562	blood:
8	chr2:78538765..78541253-chr2:78550718..78553114,2	K562	blood:
9	chr2:78326493..78328202-chr2:78333273..78335963,2	K562	blood:
10	chr2:78347906..78350697-chr2:78350756..78353381,2	K562	blood:
11	chr2:78578454..78579130-chr2:79226516..79227199,2	MCF-7	breast:
12	chr17:59624355..59624932-chr2:78345304..78345966,2	MCF-7	breast:
13	chr2:78552005..78554249-chr2:78556086..78558009,2	K562	blood:
14	chr2:78578903..78584135-chr2:78585848..78590226,6	K562	blood:
15	chr2:78347906..78350697-chr2:78350756..78353381,2	K562	blood:
16	chr2:78538765..78541253-chr2:78550718..78553114,2	K562	blood:
17	chr2:78215424..78217099-chr2:78219299..78221415,2	K562	blood:
18	chr2:78215424..78217099-chr2:78219299..78221415,2	K562	blood:
19	chr2:78519747..78522682-chr2:78785137..78786876,2	K562	blood:
20	chr2:78577011..78577791-chr8:96157456..96158424,2	MCF-7	breast:
21	chr2:78658404..78659062-chr2:79206498..79207224,3	MCF-7	breast:
22	chr2:78552005..78554249-chr2:78556086..78558009,2	K562	blood:
23	chr1:111007522..111008367-chr2:78191655..78192229,2	MCF-7	breast:
24	chr2:78347733..78349406-chr2:78351881..78353903,2	K562	blood:
25	chr2:78295743..78297764-chr2:78300068..78303067,2	K562	blood:
26	chr2:78578299..78578916-chr2:79206809..79207351,2	MCF-7	breast:
27	chr2:78637554..78639977-chr2:78766787..78768860,2	K562	blood:
28	chr2:78300847..78302731-chr2:78308537..78310502,2	K562	blood:
29	chr2:78150104..78151070-chr7:109526792..109527641,2	MCF-7	breast:
30	chr2:78658362..78658925-chr2:79089675..79090181,2	MCF-7	breast:

(count:39 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRTM4-3	chr2:78252450-78252550	NONHSAT071835
2	lnc-REG3G-4	chr2:78143060-78143219	XLOC_001542
3	lnc-LRRTM4-3	chr2:78229100-78229271	NONHSAT071835
4	lnc-REG3G-8	chr2:78174151-78174300	NONHSAT071839
5	lnc-LRRTM4-2	chr2:78176532-78176551	XLOC_002173
6	lnc-LRRTM4-3	chr2:78517514-78517857	NR_110288
7	lnc-REG3G-4	chr2:78144874-78145117	XLOC_001542
8	lnc-REG3G-3	chr2:78321763-78321902	XLOC_001543
9	lnc-LRRTM4-3	chr2:78225204-78225307	NONHSAT071835
10	lnc-LRRTM4-3	chr2:78214578-78215904	NONHSAT071835
11	lnc-REG3G-8	chr2:78169364-78169425	NONHSAT071839
12	lnc-REG3G-3	chr2:78354625-78354877	XLOC_001543
13	lnc-LRRTM4-8	chr2:78105961-78106058	ucscGeneNc_uc002snu_2
14	lnc-REG3G-4	chr2:78144363-78144530	XLOC_001542
15	lnc-REG3G-4	chr2:78144828-78145135	NONHSAT071836
16	lnc-REG3G-3	chr2:78339185-78339226	XLOC_001543
17	lnc-LRRTM4-2	chr2:78178164-78178621	XLOC_002173
18	lnc-REG3G-8	chr2:78187674-78187885	NONHSAT071839
19	lnc-REG3G-4	chr2:78143033-78143219	XLOC_001542
20	lnc-REG3G-8	chr2:78175271-78175410	NONHSAT071839
21	lnc-LRRTM4-8	chr2:78098667-78099271	ucscGeneNc_uc002snu_2
22	lnc-LRRTM4-3	chr2:78639673-78640302	NONHSAT071846
23	lnc-LRRTM4-3	chr2:78637204-78640302	NONHSAT071835
24	lnc-REG3G-4	chr2:78144829-78145134	NR_110286
25	lnc-REG3G-4	chr2:78143060-78143219	NR_110286
26	lnc-REG3G-4	chr2:78144829-78145135	XLOC_001542
27	lnc-REG3G-8	chr2:78192534-78192764	NONHSAT071839
28	lnc-REG3G-4	chr2:78143032-78143219	NONHSAT071836
29	lnc-REG3G-8	chr2:78208133-78208440	NONHSAT071839
30	lnc-REG3G-7	chr2:78664976-78666047	NONHSAT071848
31	lnc-LRRTM4-3	chr2:78102058-78102188	NONHSAT071835
32	lnc-LRRTM4-3	chr2:78102106-78102188	NR_110288
33	lnc-REG3G-3	chr2:78320703-78320792	XLOC_001543
34	lnc-REG3G-4	chr2:78144362-78144530	NONHSAT071836
35	lnc-REG3G-4	chr2:78144363-78144530	XLOC_001542
36	lnc-REG3G-4	chr2:78144363-78144530	NR_110286
37	lnc-LRRTM4-8	chr2:78371022-78371323	ucscGeneNc_uc002snu_2
38	lnc-LRRTM4-3	chr2:78639919-78640220	NONHSAT071847
39	lnc-REG3G-3	chr2:78322790-78322968	XLOC_001543

No data

Variant related genes	Relation type
CYCSP6	TF binding region
ENSG00000233605	TF binding region
ENSG00000229494	TF binding region
ENSG00000270470	TF binding region
CYCSP6	CpG island
ENSG00000233605	CpG island
ENSG00000229494	CpG island
ENSG00000270470	CpG island
PDCD4	miRNA target sites
CELF2	miRNA target sites

Extended variants
information (count: 10391 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:10391 , 50 per page) page: 1 2 3 4 5 6 7 ... 208

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574202968	chr2:78091356-78091357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs541599853	chr2:78091376-78091377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560190299	chr2:78091384-78091385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10180778	chr2:78091420-78091421	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs10204293	chr2:78091438-78091439	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs148398106	chr2:78091478-78091479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548210331	chr2:78091559-78091560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142491573	chr2:78091561-78091562	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200917165	chr2:78091625-78091626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs114705128	chr2:78091635-78091636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201614563	chr2:78091637-78091638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369019399	chr2:78091638-78091639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550508039	chr2:78091663-78091664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10181240	chr2:78091687-78091688	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs146523317	chr2:78091688-78091689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs114258764	chr2:78091705-78091706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566724342	chr2:78091735-78091736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs72913806	chr2:78091786-78091787	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs189151073	chr2:78091801-78091802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575798253	chr2:78091832-78091833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs193036626	chr2:78091857-78091858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538434729	chr2:78091878-78091879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182891353	chr2:78091891-78091892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562355278	chr2:78091922-78091923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs578245630	chr2:78091929-78091930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112363171	chr2:78091932-78091933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545841760	chr2:78091935-78091936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535631432	chr2:78091964-78091965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112401686	chr2:78091969-78091970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547599898	chr2:78091977-78091978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs13425725	chr2:78091994-78091995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374630567	chr2:78092018-78092019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs13400387	chr2:78092062-78092063	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs541914865	chr2:78092076-78092077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186616108	chr2:78092079-78092080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566146296	chr2:78092090-78092091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs13428394	chr2:78092123-78092124	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs201591494	chr2:78092130-78092131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191415852	chr2:78092139-78092140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184318198	chr2:78092140-78092141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs13403180	chr2:78092155-78092156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546542588	chr2:78092188-78092189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs13416603	chr2:78092192-78092193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535435002	chr2:78092196-78092197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs199924377	chr2:78092204-78092205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369543633	chr2:78092205-78092206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35738261	chr2:78092206-78092207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs79610997	chr2:78092209-78092210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs397712372	chr2:78092227-78092228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201077702	chr2:78092228-78092229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	18438408	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Mental retardation	17124404	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Breast cancer	16272173	CNVD
Epilepsy	22083797	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:469 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:78089600-78093800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:78091000-78091400	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr2:78091200-78091400	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr2:78091200-78091600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr2:78091200-78091600	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr2:78093800-78094000	Enhancers	Fetal Lung	lung
7	chr2:78093800-78094200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr2:78100200-78100600	Enhancers	Fetal Lung	lung
9	chr2:78100600-78102800	Weak transcription	Fetal Lung	lung
10	chr2:78101000-78101400	Enhancers	Colon Smooth Muscle	Colon
11	chr2:78102800-78104000	Enhancers	Fetal Lung	lung
12	chr2:78103400-78107800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr2:78105400-78105600	Enhancers	Pancreas	Pancrea
14	chr2:78119000-78119200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr2:78119200-78119400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr2:78124600-78125000	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr2:78124800-78125200	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr2:78124800-78125200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr2:78125200-78127200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr2:78127200-78128200	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr2:78127400-78127800	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr2:78127600-78128200	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr2:78129400-78133200	Weak transcription	Pancreas	Pancrea
24	chr2:78151800-78152000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr2:78152600-78152800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr2:78157000-78157400	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr2:78159000-78159400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr2:78159400-78160400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr2:78160400-78161200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr2:78192800-78193200	Active TSS	ES-I3 Cell Line	embryonic stem cell
31	chr2:78193200-78195000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr2:78194800-78195200	Active TSS	HUES6 Cell Line	embryonic stem cell
33	chr2:78194800-78195200	Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr2:78195000-78195200	Active TSS	ES-I3 Cell Line	embryonic stem cell
35	chr2:78195200-78195600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr2:78195200-78200200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr2:78195600-78195800	Active TSS	ES-I3 Cell Line	embryonic stem cell
38	chr2:78195800-78199600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr2:78199200-78201800	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr2:78199600-78200200	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr2:78199800-78200000	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr2:78200000-78200400	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr2:78200000-78200800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr2:78200200-78200400	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr2:78200200-78201200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr2:78200400-78200600	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr2:78200400-78201400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr2:78200600-78201000	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr2:78200600-78201800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr2:78200800-78201200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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