Variant report

Variant	nsv435740
Chromosome Location	chr20:14771603-14941933
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1528)
CpG islands
(count:61)
Chromatin interactive
region (count:46)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1528 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:14936639-14937073	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:14859363-14860384	HepG2	liver:	n/a	n/a
3	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
4	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
6	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
7	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
8	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
9	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
11	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
13	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
14	ATF3	chr20:14859536-14860398	A549	lung:	n/a	n/a
15	ATF3	chr20:14859595-14860443	A549	lung:	n/a	n/a
16	ATF3	chr20:14826094-14826569	A549	lung:	n/a	n/a
17	BACH1	chr20:14841074-14841466	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
19	BATF	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
20	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
21	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
22	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
23	BATF	chr20:14931782-14932075	GM12878	blood:	n/a	n/a
24	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
25	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
26	BATF	chr20:14860106-14860399	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
27	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
28	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
29	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
30	BATF	chr20:14860056-14860418	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
31	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
32	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
33	BATF	chr20:14810566-14810958	GM12878	blood:	n/a	n/a
34	BCL11A	chr20:14813268-14813779	GM12878	blood:	n/a	n/a
35	BCL11A	chr20:14883096-14883392	GM12878	blood:	n/a	chr20:14883229-14883238
36	BCL11A	chr20:14841111-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
37	BCL11A	chr20:14859536-14859807	GM12878	blood:	n/a	n/a
38	BCL11A	chr20:14810584-14810953	GM12878	blood:	n/a	chr20:14810705-14810714
39	BCL11A	chr20:14819269-14819704	GM12878	blood:	n/a	chr20:14819415-14819424
40	BCL11A	chr20:14813340-14813684	GM12878	blood:	n/a	n/a
41	BCL11A	chr20:14833756-14834084	GM12878	blood:	n/a	n/a
42	BCL11A	chr20:14833719-14834115	GM12878	blood:	n/a	n/a
43	BCL11A	chr20:14819190-14819731	GM12878	blood:	n/a	chr20:14819415-14819424
44	BCL11A	chr20:14811187-14811493	GM12878	blood:	n/a	n/a
45	BCL11A	chr20:14883093-14883400	GM12878	blood:	n/a	chr20:14883229-14883238
46	BCL11A	chr20:14810529-14810966	GM12878	blood:	n/a	chr20:14810705-14810714
47	BCL11A	chr20:14811061-14811585	GM12878	blood:	n/a	chr20:14811164-14811173
48	BCL3	chr20:14859514-14860394	A549	lung:	n/a	chr20:14860151-14860160 chr20:14860265-14860274
49	BCL3	chr20:14859331-14860569	A549	lung:	n/a	chr20:14860151-14860160 chr20:14859419-14859428 chr20:14860265-14860274
50	BCL3	chr20:14826038-14826561	A549	lung:	n/a	chr20:14826452-14826461

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:14904432-14904482	RPTEC	kidney:	n/a
2	chr20:14904432-14904482	HEK293	kidney:	embryo
3	chr20:14904432-14904482	HEEpiC	esophagus:	n/a
4	chr20:14904432-14904482	SK-N-SH_RA	brain:	n/a
5	chr20:14904432-14904482	GM06990	blood:	n/a
6	chr20:14904432-14904482	HRCEpiC	kidney:	n/a
7	chr20:14904432-14904482	HNPCEpiC	eye:	n/a
8	chr20:14904432-14904482	IMR90	lung:	fetal
9	chr20:14904432-14904482	H1-hESC	embryonic stem cell:	embryo
10	chr20:14904432-14904482	AG10803	skin:	n/a
11	chr20:14904432-14904482	AoSMC	blood vessel:	n/a
12	chr20:14904432-14904482	ECC-1	luminal epithelium:	n/a
13	chr20:14904432-14904482	HIPEpiC	eye:	n/a
14	chr20:14904432-14904482	PANC-1	pancreas:	n/a
15	chr20:14904432-14904482	SKMC	muscle:	n/a
16	chr20:14904432-14904482	BJ	skin:	n/a
17	chr20:14904432-14904482	GM19239	blood:	n/a
18	chr20:14904432-14904482	SK-N-SH	brain:	n/a
19	chr20:14904432-14904482	Hepatocyte	liver:	n/a
20	chr20:14904432-14904482	AG09309	skin:	n/a
21	chr20:14904432-14904482	NH-A	brain:	n/a
22	chr20:14904432-14904482	ovcar-3	ovarian:	n/a
23	chr20:14904432-14904482	PFSK-1	brain:	n/a
24	chr20:14904432-14904482	HepG2	liver:	n/a
25	chr20:14904432-14904482	AG04450	lung:	fetal
26	chr20:14904432-14904482	CMK	blood:	n/a
27	chr20:14904432-14904482	HAEpiC	amniotic membrane:	n/a
28	chr20:14904432-14904482	ProgFib	skin:	n/a
29	chr20:14904432-14904482	MCF-7	breast:	n/a
30	chr20:14904432-14904482	Jurkat	blood:	n/a
31	chr20:14904432-14904482	HCPEpiC	choroid plexus:	n/a
32	chr20:14904432-14904482	SK-N-MC	brain:	n/a
33	chr20:14904432-14904482	K562	blood:	n/a
34	chr20:14904432-14904482	NT2-D1	testis:	n/a
35	chr20:14904432-14904482	A549	lung:	n/a
36	chr20:14904432-14904482	BE2_C	brain:	n/a
37	chr20:14904432-14904482	Caco-2	colon:	n/a
38	chr20:14904432-14904482	U87	brain:	n/a
39	chr20:14904432-14904482	HL-60	blood:	n/a
40	chr20:14904432-14904482	T-47D	breast:	n/a
41	chr20:14904432-14904482	GM12891	blood:	n/a
42	chr20:14904432-14904482	HCM	heart:	n/a
43	chr20:14904432-14904482	NHBE	bronchial:	n/a
44	chr20:14904432-14904482	AG04449	skin:	fetal
45	chr20:14904432-14904482	SAEC	small airway:	n/a
46	chr20:14904432-14904482	GM12892	blood:	n/a
47	chr20:14904432-14904482	NB4	blood:	n/a
48	chr20:14904432-14904482	HUVEC	blood vessel:	n/a
49	chr20:14904432-14904482	HMEC	breast:	n/a
50	chr20:14904432-14904482	HCT-116	colon:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
2	chr20:14905161..14907169-chr20:14915982..14918854,2	MCF-7	breast:
3	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
4	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
5	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
6	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
7	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
8	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
9	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
10	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
11	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
12	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
13	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
14	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
15	chr20:14857662..14859546-chr20:15214980..15217486,2	MCF-7	breast:
16	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
17	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
18	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
19	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
20	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
21	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
22	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
23	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
24	chr20:14314384..14315320-chr20:14929469..14930347,2	MCF-7	breast:
25	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
26	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
27	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
28	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
29	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
30	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
31	chr20:14819830..14820468-chr4:11534089..11534643,2	MCF-7	breast:
32	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
33	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
34	chr20:14913183..14915031-chr20:14915260..14917096,2	MCF-7	breast:
35	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
36	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
37	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
38	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
39	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
40	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
41	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
42	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
43	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
44	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
45	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
46	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FLRT3-1	chr20:14910021-14910164	NR_037841
2	lnc-FLRT3-1	chr20:14868742-14868950	NONHSAT078721
3	lnc-FLRT3-1	chr20:14885587-14886675	ENSG00000235914.1
4	lnc-FLRT3-1	chr20:14868742-14868950	NR_037841
5	lnc-FLRT3-2	chr20:14915884-14916009	ENSG00000237832.1
6	lnc-FLRT3-1	chr20:14864896-14865240	NONHSAT078721
7	lnc-FLRT3-1	chr20:14864898-14865240	NONHSAT078722
8	lnc-FLRT3-1	chr20:14864899-14865240	NR_037841
9	lnc-FLRT3-2	chr20:14915576-14915720	ENSG00000237832.1
10	lnc-FLRT3-1	chr20:14910021-14910164	NR_072988
11	lnc-FLRT3-1	chr20:14910021-14910154	NONHSAT078722
12	lnc-FLRT3-4	chr20:14858021-14858161	ucscGeneNc_uc002woy_1
13	lnc-FLRT3-1	chr20:14868742-14868950	ENSG00000235914.1
14	lnc-FLRT3-1	chr20:14864899-14865240	NR_110318
15	lnc-FLRT3-1	chr20:14910021-14910132	ENSG00000235914.1
16	lnc-FLRT3-1	chr20:14910021-14910142	NONHSAT078721
17	lnc-FLRT3-1	chr20:14910021-14910164	NR_110318
18	lnc-FLRT3-2	chr20:14914489-14914588	ENSG00000237832.1
19	lnc-FLRT3-4	chr20:14812896-14813240	ucscGeneNc_uc002woy_1
20	lnc-C20orf7-3	chr20:14830550-14831152	NONHSAT078716
21	lnc-FLRT3-1	chr20:14864899-14865240	ENSG00000235914.1
22	lnc-FLRT3-1	chr20:14885587-14886675	NR_072988
23	lnc-C20orf7-3	chr20:14868789-14869314	NONHSAT078714
24	lnc-FLRT3-1	chr20:14910021-14910161	ENSG00000235914.1
25	lnc-FLRT3-4	chr20:14816742-14816950	ucscGeneNc_uc002woy_1
26	lnc-C20orf7-3	chr20:14830550-14830649	NONHSAT078714

No data

Variant related genes	Relation type
ENSG00000237832	TF binding region
MACROD2-AS1	TF binding region
ENSG00000237832	CpG island
MACROD2-AS1	CpG island
ENSG00000237832	chromatin interactions

Extended variants
information (count: 5098 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:5098 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551494994	chr20:14771655-14771656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540403175	chr20:14771686-14771687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371201944	chr20:14771700-14771701	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183347117	chr20:14771819-14771820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532354743	chr20:14771844-14771845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536700238	chr20:14771910-14771911	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550429799	chr20:14771940-14771941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556546558	chr20:14771947-14771948	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs74788694	chr20:14771948-14771949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187427477	chr20:14771974-14771975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566952682	chr20:14771975-14771976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs117672641	chr20:14772023-14772024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552976700	chr20:14772042-14772043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552722013	chr20:14772045-14772046	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs62204796	chr20:14772047-14772048	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373624591	chr20:14772053-14772054	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs115863735	chr20:14772122-14772123	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191840367	chr20:14772124-14772125	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs8183997	chr20:14772125-14772126	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536252158	chr20:14772172-14772173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs75501382	chr20:14772173-14772174	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs115721405	chr20:14772184-14772185	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573034261	chr20:14772218-14772219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6105328	chr20:14772262-14772263	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544875749	chr20:14772282-14772283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73264669	chr20:14772284-14772285	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs4141462	chr20:14772300-14772301	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs370946964	chr20:14772339-14772340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182533290	chr20:14772367-14772368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs16994977	chr20:14772378-14772379	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs544008227	chr20:14772533-14772534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562431547	chr20:14772560-14772561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115377532	chr20:14772584-14772585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs35149710	chr20:14772618-14772619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548156574	chr20:14772660-14772661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142145377	chr20:14772673-14772674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7269960	chr20:14772675-14772676	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs146253132	chr20:14772737-14772738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186807385	chr20:14772759-14772760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2327889	chr20:14772789-14772790	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs550444794	chr20:14772815-14772816	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568750216	chr20:14772889-14772890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2327890	chr20:14772899-14772900	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs554466540	chr20:14772937-14772938	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572724842	chr20:14772941-14772942	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192304708	chr20:14772952-14772953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558326548	chr20:14773003-14773004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs138916793	chr20:14773020-14773021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543998066	chr20:14773100-14773101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548574066	chr20:14773161-14773162	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Breast cancer	16397240	CNVD
abortions and stillbirths	19751515	CNVD
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Glaucoma	21310917	CNVD
Alagille syndrome	22470819	CNVD
Lung cancer	16773561	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Myelofibrosis	22110671	CNVD
Kabuki syndrome	21720541	CNVD
Glioblastoma multiforme	22286061	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Neurocytoma	17123091	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164919	CNVD
Multiple sclerosis	20663923	CNVD
Schizophrenia	20663923	CNVD
brain infarct	20663923	CNVD
Breast cancer	22522925	CNVD
Breast cancer	17142309	CNVD
Cancer	20164920	CNVD
Schizophrenia	23813976	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	20531469	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Williams Syndrome	20824207	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
early-passage human iPS cells	21368824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Cancer	21272361	CNVD

Chromatin state (count:905 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14770400-14772400	Enhancers	Fetal Intestine Large	intestine
2	chr20:14770600-14773000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr20:14771000-14771800	Enhancers	Small Intestine	intestine
4	chr20:14771000-14772400	Enhancers	Fetal Intestine Small	intestine
5	chr20:14771400-14772200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr20:14771400-14772200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr20:14771800-14773000	Weak transcription	Small Intestine	intestine
8	chr20:14772400-14772800	Weak transcription	Fetal Intestine Large	intestine
9	chr20:14772400-14772800	Weak transcription	Fetal Intestine Small	intestine
10	chr20:14772800-14774200	Enhancers	Fetal Intestine Small	intestine
11	chr20:14772800-14774400	Enhancers	Fetal Intestine Large	intestine
12	chr20:14773000-14773400	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr20:14773200-14773400	Enhancers	Small Intestine	intestine
14	chr20:14774600-14774800	Enhancers	Gastric	stomach
15	chr20:14780000-14780400	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr20:14780000-14780600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr20:14780200-14780600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr20:14780400-14780600	Enhancers	Fetal Brain Female	brain
19	chr20:14780600-14782200	Weak transcription	Fetal Brain Female	brain
20	chr20:14782200-14782400	Enhancers	Liver	Liver
21	chr20:14782200-14783800	Enhancers	Fetal Brain Female	brain
22	chr20:14782400-14782800	Flanking Active TSS	Liver	Liver
23	chr20:14782600-14783400	Enhancers	GM12878-XiMat	blood
24	chr20:14782800-14783000	Enhancers	Liver	Liver
25	chr20:14787600-14788000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr20:14798200-14798400	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr20:14798200-14798600	Enhancers	Fetal Kidney	kidney
28	chr20:14798400-14800400	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr20:14800400-14800800	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr20:14800800-14801400	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr20:14801200-14801800	Enhancers	Fetal Brain Male	brain
32	chr20:14801200-14801800	Enhancers	Fetal Brain Female	brain
33	chr20:14801400-14801800	Active TSS	Pancreatic Islets	Pancreatic Islet
34	chr20:14801800-14806000	Weak transcription	Fetal Brain Female	brain
35	chr20:14801800-14807400	Weak transcription	Fetal Brain Male	brain
36	chr20:14805000-14805800	Enhancers	Colon Smooth Muscle	Colon
37	chr20:14805000-14808200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr20:14805200-14805400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr20:14805200-14806400	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr20:14805400-14808200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr20:14805600-14806000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr20:14805600-14807600	Enhancers	Brain Germinal Matrix	brain
43	chr20:14805600-14807800	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr20:14805800-14806200	Enhancers	Fetal Kidney	kidney
45	chr20:14805800-14808200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr20:14806000-14806200	Enhancers	Fetal Brain Female	brain
47	chr20:14806000-14806800	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr20:14806000-14807200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr20:14806200-14806600	Weak transcription	Fetal Brain Female	brain
50	chr20:14806600-14808200	Enhancers	Fetal Brain Female	brain

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