Variant report

Variant	nsv879662
Chromosome Location	chr4:100849466-100876648
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1853)
CpG islands
(count:1530)
Chromatin interactive
region (count:99)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1853 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:100871309-100872067	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:100866794-100867174	K562	blood:	n/a	n/a
3	ARID3A	chr4:100870078-100870519	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:100865222-100865553	K562	blood:	n/a	n/a
5	ARID3A	chr4:100868101-100868534	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:100870105-100870851	K562	blood:	n/a	chr4:100870611-100870619 chr4:100870840-100870848
7	ARID3A	chr4:100868363-100868626	K562	blood:	n/a	n/a
8	ATF2	chr4:100871090-100872118	GM12878	blood:	n/a	n/a
9	ATF2	chr4:100869905-100870773	GM12878	blood:	n/a	n/a
10	ATF2	chr4:100871070-100871599	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr4:100869900-100871025	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr4:100865124-100865491	GM12878	blood:	n/a	n/a
13	ATF2	chr4:100869887-100870874	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr4:100869939-100870983	GM12878	blood:	n/a	n/a
15	ATF2	chr4:100871128-100871653	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr4:100867849-100868786	GM12878	blood:	n/a	n/a
17	ATF2	chr4:100867529-100869163	GM12878	blood:	n/a	n/a
18	ATF2	chr4:100867812-100868613	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr4:100867642-100868933	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF3	chr4:100867751-100867975	K562	blood:	n/a	n/a
21	ATF3	chr4:100870062-100870574	K562	blood:	n/a	n/a
22	ATF3	chr4:100871568-100872032	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF3	chr4:100871195-100871623	K562	blood:	n/a	n/a
24	ATF3	chr4:100871607-100871896	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF3	chr4:100871618-100871959	K562	blood:	n/a	n/a
26	ATF3	chr4:100870113-100870581	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF3	chr4:100871121-100871599	A549	lung:	n/a	n/a
28	ATF3	chr4:100870169-100870467	K562	blood:	n/a	n/a
29	BACH1	chr4:100870166-100871420	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr4:100869922-100870906	K562	blood:	n/a	n/a
31	BACH1	chr4:100868024-100868492	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr4:100872403-100872411	H1-hESC	embryonic stem cell:	n/a	n/a
33	BATF	chr4:100871187-100871533	GM12878	blood:	n/a	n/a
34	BATF	chr4:100870091-100870511	GM12878	blood:	n/a	n/a
35	BCL11A	chr4:100867600-100868432	GM12878	blood:	n/a	chr4:100868305-100868314
36	BCL3	chr4:100867870-100868837	K562	blood:	n/a	chr4:100868305-100868314
37	BCL3	chr4:100867503-100869024	A549	lung:	n/a	chr4:100868305-100868314
38	BCL3	chr4:100867607-100868557	GM12878	blood:	n/a	chr4:100868305-100868314
39	BCL3	chr4:100867862-100868404	GM12878	blood:	n/a	chr4:100868305-100868314
40	BCL3	chr4:100867855-100868460	K562	blood:	n/a	chr4:100868305-100868314
41	BCL3	chr4:100871068-100871552	A549	lung:	n/a	n/a
42	BCL3	chr4:100871169-100871628	A549	lung:	n/a	n/a
43	BCL3	chr4:100871153-100871917	GM12878	blood:	n/a	n/a
44	BCL3	chr4:100867470-100868643	A549	lung:	n/a	chr4:100868305-100868314 chr4:100867499-100867512
45	BCLAF1	chr4:100871066-100871556	GM12878	blood:	n/a	n/a
46	BCLAF1	chr4:100871104-100871558	GM12878	blood:	n/a	n/a
47	BCLAF1	chr4:100867129-100868664	GM12878	blood:	n/a	chr4:100868305-100868314 chr4:100867499-100867512
48	BCLAF1	chr4:100867518-100868520	GM12878	blood:	n/a	chr4:100868305-100868314
49	BCLAF1	chr4:100867607-100868441	K562	blood:	n/a	chr4:100868305-100868314
50	BCLAF1	chr4:100871070-100871566	K562	blood:	n/a	n/a

(count:1530 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:100871315-100871365	Jurkat	blood:	n/a
2	chr4:100870737-100870787	HCF	heart:	n/a
3	chr4:100868132-100868182	PFSK-1	brain:	n/a
4	chr4:100864777-100864827	HCT-116	colon:	n/a
5	chr4:100871484-100871534	U87	brain:	n/a
6	chr4:100871315-100871365	Jurkat	blood:	n/a
7	chr4:100870737-100870787	HCF	heart:	n/a
8	chr4:100868132-100868182	PFSK-1	brain:	n/a
9	chr4:100864777-100864827	HCT-116	colon:	n/a
10	chr4:100871484-100871534	U87	brain:	n/a
11	chr4:100868132-100868182	CMK	blood:	n/a
12	chr4:100868318-100868368	HUVEC	blood vessel:	n/a
13	chr4:100871523-100871573	U87	brain:	n/a
14	chr4:100867933-100867983	HRE	kidney:	n/a
15	chr4:100867853-100867903	K562	blood:	n/a
16	chr4:100868099-100868149	HIPEpiC	eye:	n/a
17	chr4:100868318-100868368	SKMC	muscle:	n/a
18	chr4:100867933-100867983	HMEC	breast:	n/a
19	chr4:100871523-100871573	GM12891	blood:	n/a
20	chr4:100871536-100871586	A549	lung:	n/a
21	chr4:100870750-100870800	ECC-1	luminal epithelium:	n/a
22	chr4:100871993-100872043	ovcar-3	ovarian:	n/a
23	chr4:100871150-100871200	Hepatocyte	liver:	n/a
24	chr4:100870323-100870373	AG04449	skin:	fetal
25	chr4:100870687-100870737	Caco-2	colon:	n/a
26	chr4:100867853-100867903	AG09309	skin:	n/a
27	chr4:100871993-100872043	AG04450	lung:	fetal
28	chr4:100871315-100871365	SAEC	small airway:	n/a
29	chr4:100867292-100867342	MCF10A-Er-Src	breast:	n/a
30	chr4:100868099-100868149	K562	blood:	n/a
31	chr4:100870687-100870737	Hela-S3	cervix:	n/a
32	chr4:100871150-100871200	Hela-S3	cervix:	n/a
33	chr4:100870323-100870373	ECC-1	luminal epithelium:	n/a
34	chr4:100870750-100870800	PFSK-1	brain:	n/a
35	chr4:100870642-100870692	GM12878	blood:	n/a
36	chr4:100867933-100867983	HNPCEpiC	eye:	n/a
37	chr4:100870488-100870538	HL-60	blood:	n/a
38	chr4:100867350-100867400	HCPEpiC	choroid plexus:	n/a
39	chr4:100871536-100871586	HRCEpiC	kidney:	n/a
40	chr4:100867292-100867342	AoSMC	blood vessel:	n/a
41	chr4:100871534-100871584	CMK	blood:	n/a
42	chr4:100871993-100872043	GM06990	blood:	n/a
43	chr4:100868099-100868149	HEEpiC	esophagus:	n/a
44	chr4:100871536-100871586	ovcar-3	ovarian:	n/a
45	chr4:100870750-100870800	AG04449	skin:	fetal
46	chr4:100868132-100868182	GM12892	blood:	n/a
47	chr4:100867350-100867400	NHDF-neo	bronchial:	n/a
48	chr4:100872167-100872217	Hela-S3	cervix:	n/a
49	chr4:100870323-100870373	NB4	blood:	n/a
50	chr4:100871993-100872043	SKMC	muscle:	n/a

(count:99 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:100869091..100871239-chr4:103351380..103353176,2	K562	blood:
2	chr4:100483953..100487087-chr4:100868908..100871675,3	MCF-7	breast:
3	chr4:100830733..100833112-chr4:100854057..100856497,2	K562	blood:
4	chr4:100810623..100827791-chr4:100865444..100874425,55	K562	blood:
5	chr1:153508215..153509143-chr4:100870830..100871549,2	Hela-S3	cervix:
6	chr4:100867262..100869871-chr4:100873382..100875262,2	MCF-7	breast:
7	chr4:100777426..100780201-chr4:100868427..100870605,2	K562	blood:
8	chr4:100870166..100873808-chr4:100875168..100878123,5	MCF-7	breast:
9	chr4:100856020..100858032-chr4:100868560..100871073,2	K562	blood:
10	chr4:100870517..100873586-chr4:103747603..103750269,4	K562	blood:
11	chr4:99848722..99851880-chr4:100870275..100872713,4	K562	blood:
12	chr4:100850716..100855335-chr4:100865818..100872882,15	K562	blood:
13	chr4:100784573..100786137-chr4:100870218..100872755,2	K562	blood:
14	chr4:99850379..99851880-chr4:100869996..100872136,2	K562	blood:
15	chr4:100826139..100827985-chr4:100868304..100870406,2	K562	blood:
16	chr4:100855576..100858012-chr4:100858356..100861147,2	MCF-7	breast:
17	chr4:100871315..100874297-chr4:103746830..103749271,3	K562	blood:
18	chr4:100856368..100857910-chr4:100866642..100868433,2	K562	blood:
19	chr4:100868745..100870761-chr4:100992723..100994637,2	K562	blood:
20	chr4:100483327..100486538-chr4:100869980..100873651,6	K562	blood:
21	chr4:100858344..100860711-chr4:100861423..100864092,3	K562	blood:
22	chr4:100840471..100849591-chr4:100866268..100873122,18	K562	blood:
23	chr4:100814600..100817376-chr4:100869817..100872742,4	MCF-7	breast:
24	chr18:3594416..3594966-chr4:100870767..100871374,2	Hela-S3	cervix:
25	chr4:100871249..100872202-chr9:19230443..19231402,2	Hela-S3	cervix:
26	chr4:100870905..100871510-chr5:115176773..115177440,2	NB4	blood:
27	chr17:41465854..41466380-chr4:100871612..100872319,2	NB4	blood:
28	chr19:1269051..1269796-chr4:100870870..100871604,2	Hela-S3	cervix:
29	chr17:11923049..11926004-chr4:100870025..100871677,2	MCF-7	breast:
30	chr4:100814281..100816576-chr4:100852313..100854892,3	K562	blood:
31	chr4:100849849..100851641-chr4:100861198..100863933,2	K562	blood:
32	chr11:60928578..60929452-chr4:100871222..100871899,2	Hela-S3	cervix:
33	chr4:100814213..100816552-chr4:100866797..100868818,3	MCF-7	breast:
34	chr4:100458736..100461686-chr4:100868132..100870522,2	K562	blood:
35	chr4:100814544..100816576-chr4:100853046..100854892,3	K562	blood:
36	chr17:79280417..79282564-chr4:100871183..100873116,2	MCF-7	breast:
37	chr4:100848205..100853069-chr4:100866591..100869335,5	MCF-7	breast:
38	chr4:100737053..100739337-chr4:100869822..100871487,2	K562	blood:
39	chr4:76597989..76600371-chr4:100870169..100871877,2	K562	blood:
40	chr4:100856020..100858032-chr4:100868560..100871073,2	K562	blood:
41	chr4:100849266..100851363-chr4:100851727..100854069,2	K562	blood:
42	chr12:50135277..50135820-chr4:100870509..100871438,2	Hela-S3	cervix:
43	chr4:100824278..100827001-chr4:100871760..100873443,2	K562	blood:
44	chr4:100869528..100871186-chr4:107235611..107237116,2	K562	blood:
45	chr4:100813266..100817175-chr4:100865527..100871657,11	MCF-7	breast:
46	chr3:73160104..73161068-chr4:100870920..100871540,2	Hela-S3	cervix:
47	chr1:209957820..209958586-chr4:100871003..100871812,2	Hela-S3	cervix:
48	chr4:100729924..100732920-chr4:100868919..100870955,3	K562	blood:
49	chr4:100008800..100013313-chr4:100866380..100869813,5	K562	blood:
50	chr4:100480938..100486909-chr4:100867873..100873651,15	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DAPP1-2	chr4:100871517-100873711	NONHSAT097550
2	lnc-DAPP1-2	chr4:100871680-100871837	ENSG00000245322.2
3	lnc-DAPP1-1	chr4:100871163-100871385	ENSG00000245322.2
4	lnc-DAPP1-2	chr4:100871647-100871837	ENSG00000245322.2
5	lnc-DAPP1-2	chr4:100871636-100873620	NR_002799

No data

Variant related genes	Relation type
DNAJB14	TF binding region
H2AFZ	TF binding region
ENSG00000245322	TF binding region
DNAJB14	CpG island
H2AFZ	CpG island
ENSG00000245322	CpG island
ENSG00000177337	chromatin interactions
ENSG00000207501	chromatin interactions
ENSG00000265213	chromatin interactions
ENSG00000077684	chromatin interactions
ENSG00000197956	chromatin interactions
ENSG00000138823	chromatin interactions
ENSG00000241185	chromatin interactions
ENSG00000167987	chromatin interactions
ENSG00000151247	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000137145	chromatin interactions
ENSG00000246560	chromatin interactions
ENSG00000065559	chromatin interactions
ENSG00000164032	chromatin interactions
ENSG00000138814	chromatin interactions
ENSG00000177879	chromatin interactions
ENSG00000198858	chromatin interactions
ENSG00000139644	chromatin interactions
ENSG00000120699	chromatin interactions
ENSG00000162757	chromatin interactions
ENSG00000120697	chromatin interactions
ENSG00000089902	chromatin interactions
ENSG00000250403	chromatin interactions
ENSG00000138757	chromatin interactions
ENSG00000164022	chromatin interactions
ENSG00000109270	chromatin interactions
ENSG00000172493	chromatin interactions
ENSG00000185168	chromatin interactions
ENSG00000145782	chromatin interactions
ENSG00000184900	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000138821	chromatin interactions
ENSG00000099812	chromatin interactions
ENSG00000050820	chromatin interactions
ENSG00000107821	chromatin interactions
ENSG00000109332	chromatin interactions
ENSG00000263923	chromatin interactions
ENSG00000164031	chromatin interactions
ENSG00000145354	chromatin interactions
ENSG00000248161	chromatin interactions
ENSG00000215417	chromatin interactions
ENSG00000246090	chromatin interactions
ENSG00000070190	chromatin interactions
ENSG00000245322	chromatin interactions
ENSG00000099622	chromatin interactions
ENSG00000137812	chromatin interactions
ENSG00000254531	chromatin interactions
ENSG00000145331	chromatin interactions
ENSG00000197894	chromatin interactions
ENSG00000238449	chromatin interactions
ENSG00000164024	chromatin interactions

Extended variants
information (count: 965 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:965 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17029667	chr4:100849466-100849467	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs562718263	chr4:100849492-100849493	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs370379948	chr4:100849519-100849520	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs529916464	chr4:100849562-100849563	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs17541426	chr4:100849574-100849575	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs557523596	chr4:100849588-100849589	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs578142582	chr4:100849671-100849672	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs560208337	chr4:100849674-100849675	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs527368226	chr4:100849715-100849716	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs543620321	chr4:100849842-100849843	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs568223707	chr4:100849928-100849929	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs570336546	chr4:100850130-100850131	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs531930425	chr4:100850182-100850183	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs368322320	chr4:100850197-100850198	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs373458347	chr4:100850244-100850245	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs568374948	chr4:100850256-100850257	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs150208378	chr4:100850288-100850289	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs542245234	chr4:100850289-100850290	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs566195225	chr4:100850299-100850300	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs539538586	chr4:100850396-100850397	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs189163253	chr4:100850411-100850412	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs576500449	chr4:100850448-100850449	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs138827516	chr4:100850496-100850497	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs181702842	chr4:100850497-100850498	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs112306702	chr4:100850529-100850530	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs542029405	chr4:100850584-100850585	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs370581595	chr4:100850603-100850604	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs186870962	chr4:100850604-100850605	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs560067173	chr4:100850607-100850608	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs535300855	chr4:100850676-100850677	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs545569668	chr4:100850835-100850836	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs563792983	chr4:100850852-100850853	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs531217477	chr4:100851008-100851009	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs549332590	chr4:100851012-100851013	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs542659874	chr4:100851086-100851087	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs568436420	chr4:100851092-100851093	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs76138816	chr4:100851149-100851150	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs116198413	chr4:100851158-100851159	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs142663574	chr4:100851212-100851213	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs376685515	chr4:100851233-100851234	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs144148628	chr4:100851236-100851237	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs551585624	chr4:100851237-100851238	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs570122009	chr4:100851252-100851253	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs537455787	chr4:100851398-100851399	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs113944699	chr4:100851418-100851419	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs532176960	chr4:100851453-100851454	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs555771030	chr4:100851455-100851456	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs148236621	chr4:100851508-100851509	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs565782341	chr4:100851509-100851510	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs535369723	chr4:100851550-100851551	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1575 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100816000-100867000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr4:100816000-100867000	Weak transcription	Lung	lung
3	chr4:100816200-100851400	Weak transcription	A549	lung
4	chr4:100816200-100851600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr4:100816200-100853600	Weak transcription	NHLF	lung
6	chr4:100816200-100866200	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr4:100820000-100866200	Weak transcription	Fetal Heart	heart
8	chr4:100824000-100865800	Weak transcription	Psoas Muscle	Psoas
9	chr4:100824400-100866000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr4:100824800-100854200	Weak transcription	Brain Anterior Caudate	brain
11	chr4:100827600-100856400	Weak transcription	Brain Substantia Nigra	brain
12	chr4:100828800-100866200	Weak transcription	Stomach Mucosa	stomach
13	chr4:100829200-100856400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr4:100829200-100866600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr4:100829400-100852600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr4:100829400-100856200	Weak transcription	HepG2	liver
17	chr4:100829600-100866200	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr4:100836600-100856800	Weak transcription	Spleen	Spleen
19	chr4:100836800-100851800	Strong transcription	Dnd41	blood
20	chr4:100837600-100852600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr4:100838200-100850200	Strong transcription	Primary T cells fromperipheralblood	blood
22	chr4:100838400-100850000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr4:100838400-100852000	Strong transcription	Fetal Thymus	thymus
24	chr4:100839000-100852200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr4:100839200-100855600	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr4:100839200-100857400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr4:100840000-100852800	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr4:100840000-100862600	Weak transcription	K562	blood
29	chr4:100840200-100854000	Weak transcription	Brain Germinal Matrix	brain
30	chr4:100840200-100864600	Weak transcription	Rectal Smooth Muscle	rectum
31	chr4:100840200-100865800	Weak transcription	Ovary	ovary
32	chr4:100840200-100866000	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr4:100840200-100867000	Weak transcription	Gastric	stomach
34	chr4:100840400-100850000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr4:100840400-100850400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr4:100840400-100851000	Weak transcription	Fetal Brain Male	brain
37	chr4:100840400-100851400	Weak transcription	Brain Cingulate Gyrus	brain
38	chr4:100840400-100851600	Weak transcription	Fetal Brain Female	brain
39	chr4:100840400-100852400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr4:100840400-100855000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr4:100840400-100855200	Weak transcription	Colon Smooth Muscle	Colon
42	chr4:100840400-100856400	Weak transcription	Fetal Kidney	kidney
43	chr4:100840400-100856400	Weak transcription	Stomach Smooth Muscle	stomach
44	chr4:100840400-100856800	Weak transcription	Thymus	Thymus
45	chr4:100840400-100864600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr4:100840400-100866800	Weak transcription	Aorta	Aorta
47	chr4:100840400-100867000	Weak transcription	Esophagus	oesophagus
48	chr4:100840600-100850200	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr4:100840600-100852000	Strong transcription	Monocytes-CD14+_RO01746	blood
50	chr4:100840600-100862200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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