Variant report

Variant	esv1796168
Chromosome Location	chr20:14773772-14947250
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1647)
CpG islands
(count:61)
Chromatin interactive
region (count:45)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1647 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:14859363-14860384	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:14936639-14937073	HepG2	liver:	n/a	n/a
3	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
4	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
5	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
7	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
8	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
9	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
10	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
11	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
13	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr20:14859595-14860443	A549	lung:	n/a	n/a
15	ATF3	chr20:14859536-14860398	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	chr20:14931782-14932075	GM12878	blood:	n/a	n/a
19	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
20	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
21	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
22	BATF	chr20:14860056-14860418	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
23	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
24	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
25	BATF	chr20:14860106-14860399	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
26	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
27	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
28	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
29	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
30	BATF	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
31	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
32	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
33	BATF	chr20:14810566-14810958	GM12878	blood:	n/a	n/a
34	BCL11A	chr20:14833756-14834084	GM12878	blood:	n/a	n/a
35	BCL11A	chr20:14883096-14883392	GM12878	blood:	n/a	chr20:14883229-14883238
36	BCL11A	chr20:14819269-14819704	GM12878	blood:	n/a	chr20:14819415-14819424
37	BCL11A	chr20:14813268-14813779	GM12878	blood:	n/a	n/a
38	BCL11A	chr20:14841111-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
39	BCL11A	chr20:14833719-14834115	GM12878	blood:	n/a	n/a
40	BCL11A	chr20:14859536-14859807	GM12878	blood:	n/a	n/a
41	BCL11A	chr20:14819190-14819731	GM12878	blood:	n/a	chr20:14819415-14819424
42	BCL11A	chr20:14813340-14813684	GM12878	blood:	n/a	n/a
43	BCL11A	chr20:14810529-14810966	GM12878	blood:	n/a	chr20:14810705-14810714
44	BCL11A	chr20:14810584-14810953	GM12878	blood:	n/a	chr20:14810705-14810714
45	BCL11A	chr20:14883093-14883400	GM12878	blood:	n/a	chr20:14883229-14883238
46	BCL11A	chr20:14811061-14811585	GM12878	blood:	n/a	chr20:14811164-14811173
47	BCL11A	chr20:14811187-14811493	GM12878	blood:	n/a	n/a
48	BCL3	chr20:14859514-14860394	A549	lung:	n/a	chr20:14860151-14860160 chr20:14860265-14860274
49	BCL3	chr20:14825912-14826568	A549	lung:	n/a	chr20:14826452-14826461
50	BCL3	chr20:14859331-14860569	A549	lung:	n/a	chr20:14860151-14860160 chr20:14859419-14859428 chr20:14860265-14860274

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:14904432-14904482	PrEC	prostate:	n/a
2	chr20:14904432-14904482	HAEpiC	amniotic membrane:	n/a
3	chr20:14904432-14904482	HRCEpiC	kidney:	n/a
4	chr20:14904432-14904482	PANC-1	pancreas:	n/a
5	chr20:14904432-14904482	HPAEpiC	pulmonary alveolar:	n/a
6	chr20:14904432-14904482	HL-60	blood:	n/a
7	chr20:14904432-14904482	HUVEC	blood vessel:	n/a
8	chr20:14904432-14904482	T-47D	breast:	n/a
9	chr20:14904432-14904482	HepG2	liver:	n/a
10	chr20:14904432-14904482	NH-A	brain:	n/a
11	chr20:14904432-14904482	HRPEpiC	eye:	n/a
12	chr20:14904432-14904482	Jurkat	blood:	n/a
13	chr20:14904432-14904482	GM12891	blood:	n/a
14	chr20:14904432-14904482	Hepatocyte	liver:	n/a
15	chr20:14904432-14904482	RPTEC	kidney:	n/a
16	chr20:14904432-14904482	ECC-1	luminal epithelium:	n/a
17	chr20:14904432-14904482	U87	brain:	n/a
18	chr20:14904432-14904482	NB4	blood:	n/a
19	chr20:14904432-14904482	IMR90	lung:	fetal
20	chr20:14904432-14904482	GM12892	blood:	n/a
21	chr20:14904432-14904482	HMEC	breast:	n/a
22	chr20:14904432-14904482	MCF-7	breast:	n/a
23	chr20:14904432-14904482	HRE	kidney:	n/a
24	chr20:14904432-14904482	SAEC	small airway:	n/a
25	chr20:14904432-14904482	AG04449	skin:	fetal
26	chr20:14904432-14904482	LNCaP	prostate:	n/a
27	chr20:14904432-14904482	GM19239	blood:	n/a
28	chr20:14904432-14904482	HCPEpiC	choroid plexus:	n/a
29	chr20:14904432-14904482	HEEpiC	esophagus:	n/a
30	chr20:14904432-14904482	AG09319	gingival:	n/a
31	chr20:14904432-14904482	GM06990	blood:	n/a
32	chr20:14904432-14904482	AG10803	skin:	n/a
33	chr20:14904432-14904482	HCT-116	colon:	n/a
34	chr20:14904432-14904482	Caco-2	colon:	n/a
35	chr20:14904432-14904482	A549	lung:	n/a
36	chr20:14904432-14904482	SKMC	muscle:	n/a
37	chr20:14904432-14904482	HCM	heart:	n/a
38	chr20:14904432-14904482	HCF	heart:	n/a
39	chr20:14904432-14904482	K562	blood:	n/a
40	chr20:14904432-14904482	AG04450	lung:	fetal
41	chr20:14904432-14904482	NHDF-neo	bronchial:	n/a
42	chr20:14904432-14904482	GM12878	blood:	n/a
43	chr20:14904432-14904482	BE2_C	brain:	n/a
44	chr20:14904432-14904482	SK-N-SH	brain:	n/a
45	chr20:14904432-14904482	HEK293	kidney:	embryo
46	chr20:14904432-14904482	BJ	skin:	n/a
47	chr20:14904432-14904482	ProgFib	skin:	n/a
48	chr20:14904432-14904482	ovcar-3	ovarian:	n/a
49	chr20:14904432-14904482	AoSMC	blood vessel:	n/a
50	chr20:14904432-14904482	PFSK-1	brain:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
2	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
3	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
4	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
5	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
6	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
7	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
8	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
9	chr20:14857662..14859546-chr20:15214980..15217486,2	MCF-7	breast:
10	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
11	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
12	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
13	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
14	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
15	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
16	chr20:14913183..14915031-chr20:14915260..14917096,2	MCF-7	breast:
17	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
18	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
19	chr20:14905161..14907169-chr20:14915982..14918854,2	MCF-7	breast:
20	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
21	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
22	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
23	chr20:14050662..14052329-chr20:14946506..14948938,2	MCF-7	breast:
24	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
25	chr20:14314384..14315320-chr20:14929469..14930347,2	MCF-7	breast:
26	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
27	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
28	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
29	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
30	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
31	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
32	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
33	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
34	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
35	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
36	chr20:14901786..14904742-chr20:14908050..14909865,2	MCF-7	breast:
37	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
38	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
39	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
40	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
41	chr20:14819830..14820468-chr4:11534089..11534643,2	MCF-7	breast:
42	chr20:14925222..14927929-chr20:14930721..14932848,2	MCF-7	breast:
43	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
44	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
45	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 5285 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:5285 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570192160	chr20:14773781-14773782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs539552785	chr20:14773787-14773788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551684814	chr20:14773826-14773827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs143506356	chr20:14773827-14773828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537584438	chr20:14773835-14773836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs555856563	chr20:14773851-14773852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs193225129	chr20:14773912-14773913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs137991795	chr20:14773918-14773919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs149493395	chr20:14773974-14773975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs111291550	chr20:14774037-14774038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs6042924	chr20:14774091-14774092	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs564537721	chr20:14774100-14774101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs62204797	chr20:14774157-14774158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs75285449	chr20:14774193-14774194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs114813147	chr20:14774208-14774209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571145571	chr20:14774227-14774228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs538541326	chr20:14774287-14774288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562164640	chr20:14774309-14774310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs529471999	chr20:14774317-14774318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548013088	chr20:14774324-14774325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs112288238	chr20:14774364-14774365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs566242563	chr20:14774371-14774372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs1884661	chr20:14774374-14774375	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs570081589	chr20:14774605-14774606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373990563	chr20:14774610-14774611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs184386463	chr20:14774618-14774619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555793275	chr20:14774633-14774634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567856124	chr20:14774646-14774647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs535288603	chr20:14774655-14774656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs553959389	chr20:14774672-14774673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs572229884	chr20:14774694-14774695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539682072	chr20:14774708-14774709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs117300560	chr20:14774711-14774712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs139731309	chr20:14774788-14774789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560380742	chr20:14780024-14780025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs527814775	chr20:14780127-14780128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs149439830	chr20:14780220-14780221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571028772	chr20:14780245-14780246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs73264682	chr20:14780268-14780269	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs76220407	chr20:14780293-14780294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568774909	chr20:14780296-14780297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs6079566	chr20:14780319-14780320	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs62204798	chr20:14780337-14780338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs6079567	chr20:14780425-14780426	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs566427408	chr20:14780485-14780486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533610777	chr20:14780515-14780516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs376873902	chr20:14780536-14780537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs558254924	chr20:14780563-14780564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs576585559	chr20:14780610-14780611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186432574	chr20:14780614-14780615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Cancer	21272361	CNVD

Chromatin state (count:943 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14772800-14774200	Enhancers	Fetal Intestine Small	intestine
2	chr20:14772800-14774400	Enhancers	Fetal Intestine Large	intestine
3	chr20:14774600-14774800	Enhancers	Gastric	stomach
4	chr20:14780000-14780400	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr20:14780000-14780600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr20:14780200-14780600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr20:14780400-14780600	Enhancers	Fetal Brain Female	brain
8	chr20:14780600-14782200	Weak transcription	Fetal Brain Female	brain
9	chr20:14782200-14782400	Enhancers	Liver	Liver
10	chr20:14782200-14783800	Enhancers	Fetal Brain Female	brain
11	chr20:14782400-14782800	Flanking Active TSS	Liver	Liver
12	chr20:14782600-14783400	Enhancers	GM12878-XiMat	blood
13	chr20:14782800-14783000	Enhancers	Liver	Liver
14	chr20:14787600-14788000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr20:14798200-14798400	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr20:14798200-14798600	Enhancers	Fetal Kidney	kidney
17	chr20:14798400-14800400	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr20:14800400-14800800	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr20:14800800-14801400	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr20:14801200-14801800	Enhancers	Fetal Brain Male	brain
21	chr20:14801200-14801800	Enhancers	Fetal Brain Female	brain
22	chr20:14801400-14801800	Active TSS	Pancreatic Islets	Pancreatic Islet
23	chr20:14801800-14806000	Weak transcription	Fetal Brain Female	brain
24	chr20:14801800-14807400	Weak transcription	Fetal Brain Male	brain
25	chr20:14805000-14805800	Enhancers	Colon Smooth Muscle	Colon
26	chr20:14805000-14808200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr20:14805200-14805400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr20:14805200-14806400	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr20:14805400-14808200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr20:14805600-14806000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr20:14805600-14807600	Enhancers	Brain Germinal Matrix	brain
32	chr20:14805600-14807800	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr20:14805800-14806200	Enhancers	Fetal Kidney	kidney
34	chr20:14805800-14808200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr20:14806000-14806200	Enhancers	Fetal Brain Female	brain
36	chr20:14806000-14806800	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr20:14806000-14807200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr20:14806200-14806600	Weak transcription	Fetal Brain Female	brain
39	chr20:14806600-14808200	Enhancers	Fetal Brain Female	brain
40	chr20:14807200-14808000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr20:14807200-14808200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr20:14807400-14808200	Enhancers	Fetal Brain Male	brain
43	chr20:14807600-14808000	Flanking Active TSS	Brain Germinal Matrix	brain
44	chr20:14807800-14810600	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr20:14808000-14808800	Enhancers	Brain Germinal Matrix	brain
46	chr20:14810000-14810800	Enhancers	GM12878-XiMat	blood
47	chr20:14810400-14811800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr20:14810600-14811000	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr20:14810600-14812000	Enhancers	NHEK	skin
50	chr20:14810800-14811000	Enhancers	Brain Germinal Matrix	brain

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