Variant report

Variant	nsv537132
Chromosome Location	chr4:69149648-69482831
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3103)
CpG islands
(count:2200)
Chromatin interactive
region (count:112)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:3103 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69364158-69364549	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69212206-69212462	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69386831-69387059	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69185567-69186004	K562	blood:	n/a	n/a
5	ARID3A	chr4:69241809-69241916	K562	blood:	n/a	n/a
6	ARID3A	chr4:69165746-69166230	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:69215712-69215831	K562	blood:	n/a	chr4:69215782-69215790
9	ARID3A	chr4:69215585-69216036	HepG2	liver:	n/a	chr4:69215782-69215790
10	ARID3A	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:69210304-69210353	K562	blood:	n/a	n/a
12	ARID3A	chr4:69241724-69242046	HepG2	liver:	n/a	n/a
13	ATF1	chr4:69212269-69212558	K562	blood:	n/a	n/a
14	ATF1	chr4:69226955-69227269	K562	blood:	n/a	n/a
15	ATF1	chr4:69215620-69216158	K562	blood:	n/a	chr4:69215838-69215852
16	ATF2	chr4:69215452-69216129	GM12878	blood:	n/a	chr4:69215896-69215907 chr4:69215838-69215852
17	ATF2	chr4:69274713-69275097	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr4:69215580-69216036	GM12878	blood:	n/a	chr4:69215896-69215907 chr4:69215838-69215852
19	ATF2	chr4:69271370-69272360	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr4:69269806-69270384	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr4:69271320-69273979	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr4:69272567-69273233	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr4:69273374-69273928	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr4:69275508-69277104	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr4:69274062-69274402	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr4:69215463-69216132	H1-hESC	embryonic stem cell:	n/a	chr4:69215896-69215907 chr4:69215838-69215852
27	ATF2	chr4:69215430-69216233	H1-hESC	embryonic stem cell:	n/a	chr4:69215896-69215907 chr4:69215838-69215852
28	ATF2	chr4:69269850-69270608	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr4:69214914-69215381	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr4:69165562-69165682	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr4:69215560-69216041	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr4:69207891-69208159	K562	blood:	n/a	n/a
33	BACH1	chr4:69215649-69216046	K562	blood:	n/a	n/a
34	BACH1	chr4:69316907-69317183	H1-hESC	embryonic stem cell:	n/a	chr4:69317106-69317120
35	BACH1	chr4:69166084-69166208	K562	blood:	n/a	n/a
36	BACH1	chr4:69216585-69216762	K562	blood:	n/a	n/a
37	BACH1	chr4:69318318-69318341	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr4:69165597-69165751	K562	blood:	n/a	n/a
39	BATF	chr4:69212238-69212535	GM12878	blood:	n/a	chr4:69212303-69212314 chr4:69212358-69212369
40	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
41	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
42	BATF	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
43	BATF	chr4:69364212-69364472	GM12878	blood:	n/a	n/a
44	BATF	chr4:69212136-69212549	GM12878	blood:	n/a	chr4:69212303-69212314 chr4:69212358-69212369
45	BCL11A	chr4:69275877-69276040	H1-hESC	embryonic stem cell:	n/a	n/a
46	BCL11A	chr4:69233648-69233855	H1-hESC	embryonic stem cell:	n/a	n/a
47	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
48	BCL11A	chr4:69233545-69233815	H1-hESC	embryonic stem cell:	n/a	n/a
49	BCL11A	chr4:69273602-69273847	H1-hESC	embryonic stem cell:	n/a	n/a
50	BCL3	chr4:69215396-69216133	A549	lung:	n/a	n/a

(count:2200 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69355121-69355171	ovcar-3	ovarian:	n/a
2	chr4:69179965-69180015	HUVEC	blood vessel:	n/a
3	chr4:69216077-69216127	HEK293	kidney:	embryo
4	chr4:69215912-69215962	AG09319	gingival:	n/a
5	chr4:69355121-69355171	ovcar-3	ovarian:	n/a
6	chr4:69179965-69180015	HUVEC	blood vessel:	n/a
7	chr4:69216077-69216127	HEK293	kidney:	embryo
8	chr4:69215912-69215962	AG09319	gingival:	n/a
9	chr4:69434475-69434525	SK-N-MC	brain:	n/a
10	chr4:69215753-69215803	IMR90	lung:	fetal
11	chr4:69216111-69216161	AG04450	lung:	fetal
12	chr4:69216103-69216153	AG09319	gingival:	n/a
13	chr4:69176865-69176915	CMK	blood:	n/a
14	chr4:69340916-69340966	ProgFib	skin:	n/a
15	chr4:69215753-69215803	AG04449	skin:	fetal
16	chr4:69215912-69215962	HNPCEpiC	eye:	n/a
17	chr4:69215901-69215951	HCF	heart:	n/a
18	chr4:69216018-69216068	U87	brain:	n/a
19	chr4:69239481-69239531	ProgFib	skin:	n/a
20	chr4:69215318-69215368	HIPEpiC	eye:	n/a
21	chr4:69179935-69179985	HCPEpiC	choroid plexus:	n/a
22	chr4:69435593-69435643	Hela-S3	cervix:	n/a
23	chr4:69215865-69215915	HepG2	liver:	n/a
24	chr4:69215753-69215803	AG09319	gingival:	n/a
25	chr4:69216111-69216161	MCF-7	breast:	n/a
26	chr4:69355121-69355171	GM12891	blood:	n/a
27	chr4:69215786-69215836	Hepatocyte	liver:	n/a
28	chr4:69187090-69187140	MCF-7	breast:	n/a
29	chr4:69187090-69187140	Caco-2	colon:	n/a
30	chr4:69215753-69215803	SK-N-SH_RA	brain:	n/a
31	chr4:69216018-69216068	PFSK-1	brain:	n/a
32	chr4:69215865-69215915	GM12891	blood:	n/a
33	chr4:69434475-69434525	AG09319	gingival:	n/a
34	chr4:69215786-69215836	AoSMC	blood vessel:	n/a
35	chr4:69215909-69215959	HAEpiC	amniotic membrane:	n/a
36	chr4:69215909-69215959	IMR90	lung:	fetal
37	chr4:69216111-69216161	HCF	heart:	n/a
38	chr4:69215901-69215951	RPTEC	kidney:	n/a
39	chr4:69215993-69216043	HCPEpiC	choroid plexus:	n/a
40	chr4:69215909-69215959	HRE	kidney:	n/a
41	chr4:69435593-69435643	HMEC	breast:	n/a
42	chr4:69215753-69215803	BJ	skin:	n/a
43	chr4:69215896-69215946	MCF10A-Er-Src	breast:	n/a
44	chr4:69216103-69216153	SK-N-SH_RA	brain:	n/a
45	chr4:69239481-69239531	HMEC	breast:	n/a
46	chr4:69216018-69216068	HEK293	kidney:	embryo
47	chr4:69215912-69215962	SK-N-SH	brain:	n/a
48	chr4:69340916-69340966	BJ	skin:	n/a
49	chr4:69435601-69435651	H1-hESC	embryonic stem cell:	embryo
50	chr4:69312514-69312564	HCM	heart:	n/a

(count:112 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:69193668..69196027-chr4:69216381..69218945,2	K562	blood:
2	chr4:69177090..69179857-chr4:69251602..69253290,2	MCF-7	breast:
3	chr4:69225977..69228923-chr4:69232908..69234757,2	MCF-7	breast:
4	chr4:69235222..69236888-chr4:69330787..69333108,2	MCF-7	breast:
5	chr4:69243264..69245251-chr4:69248916..69251183,2	K562	blood:
6	chr4:69326187..69328959-chr4:69331153..69333884,3	MCF-7	breast:
7	chr4:69225743..69228378-chr4:69231035..69233208,2	K562	blood:
8	chr4:69212970..69215845-chr4:69239349..69242311,2	MCF-7	breast:
9	chr4:69163114..69165945-chr4:69212940..69216263,3	K562	blood:
10	chr4:69197134..69202591-chr4:69207411..69211710,5	K562	blood:
11	chr11:62609142..62609643-chr4:69215081..69215921,2	Hela-S3	cervix:
12	chr4:69314066..69315762-chr4:69317720..69319307,2	K562	blood:
13	chr4:69213603..69215709-chr4:69245624..69247287,2	K562	blood:
14	chr4:69211043..69213753-chr4:69341284..69343236,2	K562	blood:
15	chr4:69167518..69169573-chr4:69172863..69174669,2	K562	blood:
16	chr4:69308561..69313812-chr4:69314832..69320961,6	K562	blood:
17	chr1:40042036..40042680-chr4:69215224..69215736,2	Hela-S3	cervix:
18	chr4:69293251..69295177-chr4:69318009..69319544,2	K562	blood:
19	chr4:69188337..69192029-chr4:69196790..69201126,5	K562	blood:
20	chr4:69190522..69192812-chr4:69193920..69195869,2	MCF-7	breast:
21	chr4:69208163..69209683-chr4:69233967..69235522,2	MCF-7	breast:
22	chr4:69184387..69189149-chr4:69189998..69193594,6	K562	blood:
23	chr4:69362843..69365661-chr4:69770776..69774163,4	MCF-7	breast:
24	chr21:45195495..45196196-chr4:69215418..69216293,2	Hela-S3	cervix:
25	chr1:45986990..45987747-chr4:69215457..69216399,2	Hela-S3	cervix:
26	chr4:69215797..69217317-chr4:69361139..69363891,2	MCF-7	breast:
27	chr4:69200762..69202347-chr4:69204552..69206284,2	MCF-7	breast:
28	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
29	chr4:69208163..69209683-chr4:69233967..69235522,2	MCF-7	breast:
30	chr4:69218952..69221343-chr4:69221565..69223660,2	K562	blood:
31	chr4:69212213..69214534-chr4:69225131..69226946,2	MCF-7	breast:
32	chr4:69214293..69217151-chr4:69228471..69232453,4	MCF-7	breast:
33	chr4:69152138..69154955-chr4:69200554..69203200,2	K562	blood:
34	chr4:69188337..69191371-chr4:69197664..69201126,3	K562	blood:
35	chr1:180884197..180885718-chr4:69153705..69156603,2	MCF-7	breast:
36	chr4:68794156..68795825-chr4:69317354..69319516,2	MCF-7	breast:
37	chr4:69215623..69217257-chr4:69223391..69225244,2	MCF-7	breast:
38	chr2:113031752..113034339-chr4:69209531..69211318,2	MCF-7	breast:
39	chr4:69218178..69222853-chr4:69225128..69229971,4	MCF-7	breast:
40	chr4:69261479..69263949-chr4:69265088..69267687,3	K562	blood:
41	chr4:69188150..69190673-chr4:69212848..69214663,2	K562	blood:
42	chr4:69201801..69210708-chr4:69210917..69216982,18	MCF-7	breast:
43	chr4:69152138..69154955-chr4:69200554..69203200,2	K562	blood:
44	chr4:69213512..69216500-chr4:69770884..69773457,2	MCF-7	breast:
45	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
46	chr4:69194830..69197133-chr4:69209748..69212433,2	K562	blood:
47	chr4:69314066..69315762-chr4:69317720..69319307,2	K562	blood:
48	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
49	chr4:69193856..69197351-chr4:69199834..69202897,3	K562	blood:
50	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-YTHDC1-2	chr4:69151533-69151677	NONHSAT096728
2	lnc-TMPRSS11E-2	chr4:69480137-69480731	NONHSAT096735
3	lnc-UGT2B15-3	chr4:69481111-69481855	NONHSAT096736
4	lnc-YTHDC1-1	chr4:69170061-69170657	NONHSAT096730
5	lnc-UGT2B17-1	chr4:69375159-69375392	NONHSAT096733
6	lnc-UGT2B17-1	chr4:69382627-69383365	NONHSAT096733

No data

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	YTHDC1	hsa-miR-93-5p	chr4:69178020-69178042
2	YTHDC1	hsa-miR-103a-3p	chr4:69179397-69179423
3	YTHDC1	hsa-miR-16-5p	chr4:69179396-69179418
4	YTHDC1	hsa-miR-1	chr4:69176388-69176409
5	YTHDC1	hsa-miR-93-5p	chr4:69179594-69179620
6	YTHDC1	hsa-miR-93-5p	chr4:69178392-69178416

Variant related genes	Relation type
ENSG00000249531	TF binding region
ENSG00000248639	TF binding region
TMPRSS11E	TF binding region
MT2P1	TF binding region
YTHDC1	TF binding region
ENSG00000249472	TF binding region
ENSG00000251101	TF binding region
UGT2B17	TF binding region
APOOP4	TF binding region
ENSG00000250642	TF binding region
UGT2B29P	TF binding region
ENSG00000249531	CpG island
ENSG00000248639	CpG island
TMPRSS11E	CpG island
MT2P1	CpG island
YTHDC1	CpG island
ENSG00000249472	CpG island
ENSG00000251101	CpG island
UGT2B17	CpG island
APOOP4	CpG island
ENSG00000250642	CpG island
UGT2B29P	CpG island
ENSG00000249985	chromatin interactions
ENSG00000090621	chromatin interactions
ENSG00000160213	chromatin interactions
ENSG00000087128	chromatin interactions
ENSG00000234741	chromatin interactions
ENSG00000083312	chromatin interactions
ENSG00000162840	chromatin interactions
ENSG00000249531	chromatin interactions
ENSG00000188177	chromatin interactions
ENSG00000257103	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000185278	chromatin interactions
ENSG00000083896	chromatin interactions
ENSG00000117450	chromatin interactions
ENSG00000272626	chromatin interactions
ENSG00000248122	chromatin interactions

Extended variants
information (count: 11243 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:11243 , 50 per page) page: 1 2 3 4 5 6 7 ... 225

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561208607	chr4:69149658-69149659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557723950	chr4:69149664-69149665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs376031101	chr4:69149665-69149666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs368710920	chr4:69149678-69149679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs186612789	chr4:69149721-69149722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs111294129	chr4:69149753-69149754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs34550598	chr4:69149767-69149768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147842672	chr4:69149777-69149778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs28404393	chr4:69149822-69149823	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs148910179	chr4:69149835-69149836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577612284	chr4:69149859-69149860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs527654281	chr4:69149881-69149882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs192739921	chr4:69149929-69149930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs567933844	chr4:69149995-69149996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs543024011	chr4:69150065-69150066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs7671950	chr4:69150105-69150106	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs143542985	chr4:69150151-69150152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs11729143	chr4:69150214-69150215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76013951	chr4:69150221-69150222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs148046364	chr4:69150301-69150302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558650682	chr4:69150311-69150312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs7672364	chr4:69150317-69150318	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs184521906	chr4:69150344-69150345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs571446861	chr4:69150350-69150351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs574664000	chr4:69150368-69150369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs140831215	chr4:69150389-69150390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189839830	chr4:69150431-69150432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532142293	chr4:69150441-69150442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545122010	chr4:69150443-69150444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs548613500	chr4:69150457-69150458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs33912975	chr4:69150458-69150459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs565018530	chr4:69150489-69150490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs145032358	chr4:69150510-69150511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547761173	chr4:69150532-69150533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs373622713	chr4:69150563-69150564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs13145544	chr4:69150578-69150579	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs530426227	chr4:69150586-69150587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs138876655	chr4:69150622-69150623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs570278294	chr4:69150743-69150744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181394316	chr4:69150826-69150827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs141926633	chr4:69150834-69150835	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552329383	chr4:69150886-69150887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184213618	chr4:69150889-69150890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146310424	chr4:69150901-69150902	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554544203	chr4:69150903-69150904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528579524	chr4:69150920-69150921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568726063	chr4:69150930-69150931	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34300469	chr4:69150986-69150987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574303954	chr4:69150991-69150992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs114050211	chr4:69150993-69150994	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Oral cancer	21386901	CNVD
Alcoholism	21790672	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
Autism	19287141	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Ollier disease	21235737	CNVD
Autism	21865298	CNVD
Rett syndrome	21593744	CNVD
Urothelial carcinoma	21177765	CNVD
Incontinentia Pigmenti	22033527	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Medulloblastoma	21163964	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD

Chromatin state (count:3347 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69139600-69153600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr4:69148600-69151600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr4:69148800-69151000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:69149000-69151200	Enhancers	NHEK	skin
5	chr4:69149200-69150800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr4:69149400-69150200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr4:69149400-69150600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr4:69149400-69153600	Weak transcription	Fetal Intestine Large	intestine
9	chr4:69149400-69153600	Weak transcription	Fetal Intestine Small	intestine
10	chr4:69149600-69149800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr4:69149600-69149800	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr4:69149600-69150200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr4:69149800-69150600	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr4:69149800-69150600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr4:69150200-69150800	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr4:69150600-69151200	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr4:69150600-69151400	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr4:69150600-69151800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr4:69150800-69151000	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr4:69150800-69151200	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr4:69150800-69151200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr4:69150800-69151200	Enhancers	H9 Cell Line	embryonic stem cell
23	chr4:69151000-69153400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr4:69151200-69152200	Weak transcription	NHEK	skin
25	chr4:69151200-69153600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr4:69151200-69157600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr4:69151800-69155000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr4:69152200-69152400	Enhancers	NHEK	skin
29	chr4:69153200-69154600	Enhancers	HSMMtube	muscle
30	chr4:69153400-69154400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr4:69153400-69154400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr4:69153400-69154800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr4:69153600-69153800	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr4:69153600-69153800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr4:69153600-69154000	Enhancers	Fetal Intestine Small	intestine
36	chr4:69153600-69154200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:69153600-69154200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr4:69153600-69154400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr4:69153600-69154400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr4:69153600-69154400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr4:69153600-69154400	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr4:69153600-69154600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr4:69153600-69154600	Enhancers	Fetal Intestine Large	intestine
44	chr4:69153800-69154400	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr4:69154800-69155200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr4:69157600-69158200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
47	chr4:69158200-69162800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr4:69161400-69161600	Enhancers	HepG2	liver
49	chr4:69161600-69161800	Bivalent Enhancer	HepG2	liver
50	chr4:69165200-69167000	Enhancers	HepG2	liver

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