Variant report

Variant	nsv909387
Chromosome Location	chr18:11953187-11986557
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1352)
CpG islands
(count:793)
Chromatin interactive
region (count:51)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1352 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:11955409-11955965	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:11970464-11970725	K562	blood:	n/a	n/a
3	ARID3A	chr18:11982059-11982245	K562	blood:	n/a	n/a
4	ARID3A	chr18:11981074-11981228	K562	blood:	n/a	n/a
5	ARID3A	chr18:11953120-11953369	K562	blood:	n/a	n/a
6	ARID3A	chr18:11954974-11955062	K562	blood:	n/a	n/a
7	ARID3A	chr18:11980098-11981249	HepG2	liver:	n/a	n/a
8	ARID3A	chr18:11981509-11981627	HepG2	liver:	n/a	n/a
9	ARID3A	chr18:11955577-11955916	K562	blood:	n/a	n/a
10	ARID3A	chr18:11981872-11982212	HepG2	liver:	n/a	n/a
11	ARID3A	chr18:11962438-11963239	K562	blood:	n/a	n/a
12	ATF1	chr18:11953081-11953528	K562	blood:	n/a	n/a
13	ATF2	chr18:11980997-11981334	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr18:11953195-11953438	K562	blood:	n/a	chr18:11953305-11953316
15	ATF3	chr18:11955638-11955962	K562	blood:	n/a	n/a
16	ATF3	chr18:11955691-11955826	HepG2	liver:	n/a	n/a
17	BACH1	chr18:11981477-11981827	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr18:11980511-11981154	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr18:11955589-11956009	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr18:11955675-11955923	K562	blood:	n/a	n/a
21	BACH1	chr18:11956846-11957129	H1-hESC	embryonic stem cell:	n/a	n/a
22	BCL3	chr18:11980164-11980758	A549	lung:	n/a	n/a
23	BHLHE40	chr18:11980187-11982174	HepG2	liver:	n/a	chr18:11981850-11981866 chr18:11981036-11981052 chr18:11981211-11981227 chr18:11981874-11981890 chr18:11981998-11982019
24	BHLHE40	chr18:11963975-11964095	K562	blood:	n/a	n/a
25	BHLHE40	chr18:11980164-11981997	K562	blood:	n/a	chr18:11981850-11981866 chr18:11981036-11981052 chr18:11981211-11981227 chr18:11981874-11981890
26	BHLHE40	chr18:11980809-11981007	HepG2	liver:	n/a	n/a
27	BHLHE40	chr18:11953104-11953451	K562	blood:	n/a	n/a
28	BHLHE40	chr18:11980710-11980975	A549	lung:	n/a	n/a
29	BHLHE40	chr18:11980691-11981096	HepG2	liver:	n/a	chr18:11981036-11981052
30	BHLHE40	chr18:11955717-11955917	K562	blood:	n/a	n/a
31	BHLHE40	chr18:11961014-11961280	K562	blood:	n/a	n/a
32	BHLHE40	chr18:11980262-11981244	GM12878	blood:	n/a	chr18:11981036-11981052 chr18:11981211-11981227
33	BRCA1	chr18:11982270-11982505	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr18:11981000-11981235	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr18:11980153-11981274	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr18:11962539-11962972	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr18:11981580-11981624	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr18:11981634-11981834	HepG2	liver:	n/a	n/a
39	BRCA1	chr18:11980723-11980938	HepG2	liver:	n/a	n/a
40	BRCA1	chr18:11976783-11977264	Hela-S3	cervix:	n/a	n/a
41	CBX3	chr18:11953113-11953459	K562	blood:	n/a	n/a
42	CBX3	chr18:11956812-11957336	K562	blood:	n/a	n/a
43	CBX3	chr18:11981363-11981705	K562	blood:	n/a	n/a
44	CBX3	chr18:11956823-11957403	HCT-116	colon:	n/a	n/a
45	CBX3	chr18:11980391-11980692	K562	blood:	n/a	n/a
46	CBX3	chr18:11956613-11957392	K562	blood:	n/a	n/a
47	CBX3	chr18:11980201-11981327	K562	blood:	n/a	n/a
48	CCNT2	chr18:11980270-11982103	K562	blood:	n/a	chr18:11981114-11981123 chr18:11980933-11980942 chr18:11981191-11981200
49	CCNT2	chr18:11962654-11962915	K562	blood:	n/a	chr18:11962818-11962827
50	CCNT2	chr18:11961007-11961207	K562	blood:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:11980297-11980347	AG04450	lung:	fetal
2	chr18:11981591-11981641	HCT-116	colon:	n/a
3	chr18:11985726-11985776	HEEpiC	esophagus:	n/a
4	chr18:11980981-11981031	HRCEpiC	kidney:	n/a
5	chr18:11978319-11978369	BJ	skin:	n/a
6	chr18:11980953-11981003	IMR90	lung:	fetal
7	chr18:11980297-11980347	BE2_C	brain:	n/a
8	chr18:11981389-11981439	AG10803	skin:	n/a
9	chr18:11985726-11985776	PANC-1	pancreas:	n/a
10	chr18:11981602-11981652	SK-N-MC	brain:	n/a
11	chr18:11981591-11981641	AG04449	skin:	fetal
12	chr18:11981591-11981641	Jurkat	blood:	n/a
13	chr18:11980690-11980740	BE2_C	brain:	n/a
14	chr18:11981317-11981367	GM19239	blood:	n/a
15	chr18:11980953-11981003	SK-N-MC	brain:	n/a
16	chr18:11982063-11982113	GM12891	blood:	n/a
17	chr18:11980690-11980740	HUVEC	blood vessel:	n/a
18	chr18:11981591-11981641	SKMC	muscle:	n/a
19	chr18:11982063-11982113	HepG2	liver:	n/a
20	chr18:11985726-11985776	HRE	kidney:	n/a
21	chr18:11978319-11978369	HPAEpiC	pulmonary alveolar:	n/a
22	chr18:11981591-11981641	AG10803	skin:	n/a
23	chr18:11978319-11978369	AoSMC	blood vessel:	n/a
24	chr18:11981317-11981367	HEK293	kidney:	embryo
25	chr18:11980953-11981003	H1-hESC	embryonic stem cell:	embryo
26	chr18:11981591-11981641	ECC-1	luminal epithelium:	n/a
27	chr18:11981389-11981439	HepG2	liver:	n/a
28	chr18:11978319-11978369	HL-60	blood:	n/a
29	chr18:11981317-11981367	GM12891	blood:	n/a
30	chr18:11980297-11980347	LNCaP	prostate:	n/a
31	chr18:11981602-11981652	PANC-1	pancreas:	n/a
32	chr18:11982063-11982113	AG09309	skin:	n/a
33	chr18:11981317-11981367	HCF	heart:	n/a
34	chr18:11980953-11981003	BJ	skin:	n/a
35	chr18:11980981-11981031	LNCaP	prostate:	n/a
36	chr18:11981602-11981652	RPTEC	kidney:	n/a
37	chr18:11980297-11980347	HEEpiC	esophagus:	n/a
38	chr18:11981591-11981641	ovcar-3	ovarian:	n/a
39	chr18:11980297-11980347	HCT-116	colon:	n/a
40	chr18:11978319-11978369	ECC-1	luminal epithelium:	n/a
41	chr18:11982241-11982291	AG10803	skin:	n/a
42	chr18:11978319-11978369	HAEpiC	amniotic membrane:	n/a
43	chr18:11981591-11981641	GM12891	blood:	n/a
44	chr18:11980953-11981003	U87	brain:	n/a
45	chr18:11981317-11981367	SK-N-SH	brain:	n/a
46	chr18:11980690-11980740	AG09319	gingival:	n/a
47	chr18:11980981-11981031	K562	blood:	n/a
48	chr18:11981196-11981246	AG04450	lung:	fetal
49	chr18:11980690-11980740	NHDF-neo	bronchial:	n/a
50	chr18:11985726-11985776	HIPEpiC	eye:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr18:11961487..11963465-chr18:11979793..11981920,2	K562	blood:
2	chr18:11972047..11973789-chr18:11978802..11980433,2	MCF-7	breast:
3	chr18:11906925..11910950-chr18:11978930..11983753,7	MCF-7	breast:
4	chr18:11979366..11983605-chr18:11984399..11987435,4	MCF-7	breast:
5	chr18:11937666..11938178-chr18:11980436..11980995,2	MCF-7	breast:
6	chr18:11977841..11980802-chr18:11983345..11984923,2	MCF-7	breast:
7	chr18:11981732..11982258-chr7:137687279..137688011,2	Hela-S3	cervix:
8	chr18:11980301..11981116-chr8:80942163..80942686,2	Hela-S3	cervix:
9	chr18:11972504..11978571-chr18:11978817..11983017,10	K562	blood:
10	chr18:11906857..11909388-chr18:11984502..11986604,2	K562	blood:
11	chr18:11848574..11852252-chr18:11979272..11982648,7	K562	blood:
12	chr18:11978568..11983192-chr18:11993805..11998306,5	MCF-7	breast:
13	chr1:157107368..157108324-chr18:11981553..11982331,2	Hela-S3	cervix:
14	chr18:11906869..11908788-chr18:11979428..11982249,2	K562	blood:
15	chr18:11851619..11853678-chr18:11981084..11983023,2	MCF-7	breast:
16	chr18:11967810..11971954-chr18:11978967..11982085,5	K562	blood:
17	chr18:11970057..11972089-chr18:11979053..11982346,3	K562	blood:
18	chr18:11951098..11953868-chr18:11983215..11985135,2	K562	blood:
19	chr11:62608590..62609137-chr18:11976275..11977248,2	Hela-S3	cervix:
20	chr18:11978886..11981038-chr18:11986460..11988368,2	MCF-7	breast:
21	chr18:11952790..11957780-chr18:11977949..11982684,7	K562	blood:
22	chr18:11979089..11980849-chr18:12109709..12111299,2	K562	blood:
23	chr1:24285780..24286361-chr18:11980215..11981116,2	Hela-S3	cervix:
24	chr12:6579509..6580224-chr18:11980779..11981594,2	Hela-S3	cervix:
25	chr14:24682206..24682834-chr18:11980405..11981236,2	Hela-S3	cervix:
26	chr18:11972047..11973789-chr18:11978802..11980433,2	MCF-7	breast:
27	chr18:11945202..11946852-chr18:11982600..11984410,2	K562	blood:
28	chr18:11905898..11908508-chr18:11980358..11982828,3	K562	blood:
29	chr18:11961001..11963298-chr18:11980089..11982172,2	K562	blood:
30	chr18:11950713..11953292-chr18:11962814..11965398,2	K562	blood:
31	chr18:11955876..11958355-chr18:11979083..11981244,2	MCF-7	breast:
32	chr18:11980686..11981570-chr3:149530416..149530989,2	Hela-S3	cervix:
33	chr1:104068529..104069287-chr18:11980099..11980792,2	Hela-S3	cervix:
34	chr18:11972504..11976144-chr18:11977097..11981347,7	K562	blood:
35	chr1:28832088..28833058-chr18:11980322..11980977,2	Hela-S3	cervix:
36	chr18:11968537..11977808-chr18:11979434..11985075,12	MCF-7	breast:
37	chr18:11981635..11982452-chr8:37962701..37963302,2	Hela-S3	cervix:
38	chr18:11908235..11908915-chr18:11980031..11980748,2	Hela-S3	cervix:
39	chr18:11945871..11949775-chr18:11972448..11976477,3	K562	blood:
40	chr18:11979171..11983679-chr18:11993501..11995734,4	MCF-7	breast:
41	chr11:65194558..65195488-chr18:11979959..11980471,2	Hela-S3	cervix:
42	chr18:11954134..11957733-chr18:11976816..11981854,6	K562	blood:
43	chr18:11951098..11953868-chr18:11983215..11985135,2	K562	blood:
44	chr18:11848937..11853647-chr18:11979272..11982109,5	K562	blood:
45	chr18:11977841..11980802-chr18:11983345..11984923,2	MCF-7	breast:
46	chr18:11979615..11982143-chr18:12376173..12378788,2	K562	blood:
47	chr18:11981504..11983527-chr18:11985199..11986981,3	MCF-7	breast:
48	chr18:11950713..11953292-chr18:11962814..11965398,2	K562	blood:
49	chr18:11907678..11909849-chr18:11954112..11955972,2	MCF-7	breast:
50	chr18:11907153..11910661-chr18:11980045..11982514,4	MCF-7	breast:

No data

Variant related genes	Relation type
IMPA2	TF binding region
IMPA2	CpG island
ENSG00000189266	chromatin interactions
ENSG00000267165	chromatin interactions
ENSG00000082996	chromatin interactions
ENSG00000180198	chromatin interactions
ENSG00000254692	chromatin interactions
ENSG00000147586	chromatin interactions
ENSG00000117036	chromatin interactions
ENSG00000273141	chromatin interactions
ENSG00000141385	chromatin interactions
ENSG00000242125	chromatin interactions
ENSG00000254505	chromatin interactions
ENSG00000255112	chromatin interactions
ENSG00000266955	chromatin interactions
ENSG00000154889	chromatin interactions
ENSG00000141401	chromatin interactions
ENSG00000185946	chromatin interactions
ENSG00000139190	chromatin interactions
ENSG00000129691	chromatin interactions

Extended variants
information (count: 1539 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1539 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs661885	chr18:11953187-11953188	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs571641717	chr18:11953204-11953205	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs8091608	chr18:11953285-11953286	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs557179824	chr18:11953286-11953287	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs551727679	chr18:11953309-11953310	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs149489197	chr18:11953321-11953322	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs534212530	chr18:11953327-11953328	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs35457377	chr18:11953350-11953351	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs143924021	chr18:11953388-11953389	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs573848833	chr18:11953399-11953400	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs9948689	chr18:11953407-11953408	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs115605574	chr18:11953412-11953413	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs148613521	chr18:11953444-11953445	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs544824425	chr18:11953472-11953473	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs78317115	chr18:11953481-11953482	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs554829923	chr18:11953531-11953532	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs572082556	chr18:11953550-11953551	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs590081	chr18:11953557-11953558	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs11660354	chr18:11953572-11953573	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs370590028	chr18:11953603-11953604	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs577474019	chr18:11953622-11953623	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs533914887	chr18:11953625-11953626	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs139809502	chr18:11953635-11953636	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs145287407	chr18:11953637-11953638	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs552971207	chr18:11953678-11953679	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs551623507	chr18:11953687-11953688	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs8092247	chr18:11953745-11953746	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs397858554	chr18:11953782-11953783	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs369871756	chr18:11953825-11953826	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs648496	chr18:11953840-11953841	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs549232378	chr18:11953850-11953851	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs8092387	chr18:11953857-11953858	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs538175464	chr18:11953865-11953866	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs556715306	chr18:11953866-11953867	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs571791446	chr18:11953890-11953891	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs538689874	chr18:11953914-11953915	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs553590390	chr18:11953922-11953923	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs572045066	chr18:11953923-11953924	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs34511527	chr18:11953928-11953929	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs573740392	chr18:11953932-11953933	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs11341988	chr18:11953947-11953948	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs542657602	chr18:11953959-11953960	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs554637555	chr18:11953963-11953964	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs71350481	chr18:11953965-11953966	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs539289748	chr18:11953966-11953967	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs374153244	chr18:11953976-11953977	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs368702595	chr18:11953977-11953978	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs149802863	chr18:11953992-11953993	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs111774169	chr18:11953997-11953998	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs560233942	chr18:11954007-11954008	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1174 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:11947800-11954600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr18:11947800-11955000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr18:11948000-11954400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr18:11949000-11954000	Weak transcription	HSMMtube	muscle
5	chr18:11949200-11954200	Weak transcription	NHDF-Ad	bronchial
6	chr18:11949200-11954800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr18:11949200-11954800	Weak transcription	Adipose Nuclei	Adipose
8	chr18:11949200-11957000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr18:11949400-11954000	Weak transcription	HSMM	muscle
10	chr18:11949400-11954800	Weak transcription	NH-A	brain
11	chr18:11949400-11955000	Weak transcription	NHLF	lung
12	chr18:11949400-11955400	Weak transcription	Fetal Lung	lung
13	chr18:11949800-11954000	Weak transcription	Osteobl	bone
14	chr18:11949800-11954200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr18:11950600-11954000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr18:11951000-11956600	Enhancers	Placenta	Placenta
17	chr18:11952000-11953200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr18:11952000-11954000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr18:11952000-11954000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr18:11952000-11954800	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr18:11952000-11955400	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr18:11952000-11955400	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr18:11952000-11955400	Weak transcription	Fetal Stomach	stomach
24	chr18:11952000-11955800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr18:11952200-11953600	Enhancers	K562	blood
26	chr18:11952200-11954400	Weak transcription	Fetal Muscle Leg	muscle
27	chr18:11952200-11954800	Weak transcription	Psoas Muscle	Psoas
28	chr18:11952200-11954800	Enhancers	NHEK	skin
29	chr18:11952200-11955400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr18:11952200-11955400	Weak transcription	Pancreas	Pancrea
31	chr18:11952200-11962400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr18:11952200-11964000	Weak transcription	Fetal Muscle Trunk	muscle
33	chr18:11952400-11953200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr18:11952400-11953200	Weak transcription	Hela-S3	cervix
35	chr18:11952400-11954000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr18:11952400-11954400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr18:11952400-11954400	Weak transcription	A549	lung
38	chr18:11952400-11954600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr18:11952400-11955000	Weak transcription	HepG2	liver
40	chr18:11952400-11955400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr18:11952400-11955400	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr18:11952600-11954000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr18:11953200-11953400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr18:11953200-11953800	Weak transcription	Duodenum Smooth Muscle	Duodenum
45	chr18:11953200-11954200	Enhancers	Hela-S3	cervix
46	chr18:11953200-11954800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr18:11953400-11953800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr18:11953600-11954600	Weak transcription	K562	blood
49	chr18:11953800-11954400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr18:11954000-11954800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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