Variant report

Variant	nsv1062911
Chromosome Location	chr18:7561991-8088274
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4878)
CpG islands
(count:1221)
Chromatin interactive
region (count:74)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4878 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:7567159-7567359	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:7789923-7790193	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:7646125-7646628	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:7914817-7915371	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:7922278-7922695	HepG2	liver:	n/a	n/a
6	ARID3A	chr18:7755669-7756066	HepG2	liver:	n/a	n/a
7	ARID3A	chr18:7754639-7755251	HepG2	liver:	n/a	n/a
8	ARID3A	chr18:7926550-7926840	HepG2	liver:	n/a	n/a
9	ARID3A	chr18:7803881-7804600	HepG2	liver:	n/a	chr18:7804471-7804487
10	ARID3A	chr18:7657825-7658294	HepG2	liver:	n/a	n/a
11	ARID3A	chr18:7637234-7637834	HepG2	liver:	n/a	n/a
12	ARID3A	chr18:7877678-7877949	HepG2	liver:	n/a	n/a
13	ARID3A	chr18:7856771-7856951	HepG2	liver:	n/a	n/a
14	ARID3A	chr18:7575137-7575406	HepG2	liver:	n/a	n/a
15	ARID3A	chr18:7626201-7627326	HepG2	liver:	n/a	n/a
16	ARID3A	chr18:7567223-7567257	K562	blood:	n/a	n/a
17	ARID3A	chr18:7919650-7920085	HepG2	liver:	n/a	n/a
18	ARID3A	chr18:7945913-7946191	HepG2	liver:	n/a	n/a
19	ARID3A	chr18:7854850-7854870	HepG2	liver:	n/a	n/a
20	ARID3A	chr18:7749782-7750123	HepG2	liver:	n/a	n/a
21	ARID3A	chr18:7761326-7761693	HepG2	liver:	n/a	n/a
22	ARID3A	chr18:7872484-7873019	HepG2	liver:	n/a	n/a
23	ARID3A	chr18:7812328-7812873	HepG2	liver:	n/a	n/a
24	ATF1	chr18:7962387-7962390	K562	blood:	n/a	n/a
25	ATF1	chr18:7978481-7978634	K562	blood:	n/a	n/a
26	ATF1	chr18:7830466-7830793	K562	blood:	n/a	n/a
27	ATF1	chr18:8033445-8033599	K562	blood:	n/a	n/a
28	ATF2	chr18:8084225-8084553	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr18:7577712-7578133	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr18:7577742-7578206	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr18:8084143-8084544	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr18:7953060-7953502	GM12878	blood:	n/a	n/a
33	ATF3	chr18:7877593-7878025	A549	lung:	n/a	n/a
34	ATF3	chr18:7919509-7919967	A549	lung:	n/a	n/a
35	ATF3	chr18:7567156-7567368	K562	blood:	n/a	chr18:7567347-7567356 chr18:7567273-7567283
36	ATF3	chr18:7922218-7922754	A549	lung:	n/a	n/a
37	ATF3	chr18:7922221-7922773	A549	lung:	n/a	n/a
38	BACH1	chr18:8004034-8004181	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr18:7637791-7637849	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr18:7666190-7666511	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr18:7568581-7568843	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr18:7575526-7576005	H1-hESC	embryonic stem cell:	n/a	chr18:7575877-7575891
43	BACH1	chr18:7566548-7566660	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr18:7843813-7843929	K562	blood:	n/a	n/a
45	BACH1	chr18:7566904-7567617	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr18:7789903-7790543	H1-hESC	embryonic stem cell:	n/a	n/a
47	BATF	chr18:7711514-7711726	GM12878	blood:	n/a	n/a
48	BATF	chr18:7953035-7953566	GM12878	blood:	n/a	chr18:7953483-7953491
49	BATF	chr18:7953094-7953500	GM12878	blood:	n/a	chr18:7953483-7953491
50	BATF	chr18:7958495-7958781	GM12878	blood:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:7567548-7567598	HNPCEpiC	eye:	n/a
2	chr18:7567548-7567598	HNPCEpiC	eye:	n/a
3	chr18:8069731-8069781	ovcar-3	ovarian:	n/a
4	chr18:7567717-7567767	MCF10A-Er-Src	breast:	n/a
5	chr18:7567717-7567767	HCT-116	colon:	n/a
6	chr18:7563847-7563897	HAEpiC	amniotic membrane:	n/a
7	chr18:7568186-7568236	T-47D	breast:	n/a
8	chr18:7717669-7717719	GM19239	blood:	n/a
9	chr18:7568186-7568236	HCT-116	colon:	n/a
10	chr18:7568186-7568236	Caco-2	colon:	n/a
11	chr18:7566781-7566831	ECC-1	luminal epithelium:	n/a
12	chr18:7568891-7568941	HRPEpiC	eye:	n/a
13	chr18:7567548-7567598	RPTEC	kidney:	n/a
14	chr18:7567799-7567849	SAEC	small airway:	n/a
15	chr18:7567799-7567849	SK-N-MC	brain:	n/a
16	chr18:7566258-7566308	HCT-116	colon:	n/a
17	chr18:7568186-7568236	HUVEC	blood vessel:	n/a
18	chr18:7567426-7567476	HepG2	liver:	n/a
19	chr18:7568186-7568236	AG10803	skin:	n/a
20	chr18:7567799-7567849	SKMC	muscle:	n/a
21	chr18:7566558-7566608	IMR90	lung:	fetal
22	chr18:7566656-7566706	HRE	kidney:	n/a
23	chr18:7567799-7567849	A549	lung:	n/a
24	chr18:7717669-7717719	T-47D	breast:	n/a
25	chr18:7567717-7567767	NT2-D1	testis:	n/a
26	chr18:7566558-7566608	NT2-D1	testis:	n/a
27	chr18:7563847-7563897	MCF-7	breast:	n/a
28	chr18:7979736-7979786	RPTEC	kidney:	n/a
29	chr18:7567717-7567767	AG10803	skin:	n/a
30	chr18:7568539-7568589	GM12892	blood:	n/a
31	chr18:7568891-7568941	HUVEC	blood vessel:	n/a
32	chr18:7568159-7568209	HEK293	kidney:	embryo
33	chr18:7568186-7568236	SK-N-SH	brain:	n/a
34	chr18:7568186-7568236	PFSK-1	brain:	n/a
35	chr18:7717669-7717719	A549	lung:	n/a
36	chr18:7680662-7680712	HIPEpiC	eye:	n/a
37	chr18:7567799-7567849	PrEC	prostate:	n/a
38	chr18:7568159-7568209	GM19239	blood:	n/a
39	chr18:7563847-7563897	HEEpiC	esophagus:	n/a
40	chr18:7568159-7568209	SK-N-SH_RA	brain:	n/a
41	chr18:7568891-7568941	PrEC	prostate:	n/a
42	chr18:7568159-7568209	GM12892	blood:	n/a
43	chr18:7567426-7567476	SK-N-MC	brain:	n/a
44	chr18:7566558-7566608	HMEC	breast:	n/a
45	chr18:7567717-7567767	A549	lung:	n/a
46	chr18:7563847-7563897	IMR90	lung:	fetal
47	chr18:7568891-7568941	A549	lung:	n/a
48	chr18:7568891-7568941	AG09319	gingival:	n/a
49	chr18:7568186-7568236	K562	blood:	n/a
50	chr18:8069731-8069781	SK-N-SH_RA	brain:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr18:7912955..7915835-chr18:7928834..7931488,2	K562	blood:
2	chr18:8083548..8084811-chr18:8389384..8390298,8	MCF-7	breast:
3	chr18:7684763..7686884-chr18:7689927..7692256,2	K562	blood:
4	chr18:7919128..7921184-chr18:7922798..7925622,2	K562	blood:
5	chr18:7789635..7790445-chr18:8480180..8481061,3	MCF-7	breast:
6	chr18:7673185..7674687-chr18:7676145..7677987,2	K562	blood:
7	chr18:7749744..7751445-chr18:7751627..7754409,2	MCF-7	breast:
8	chr18:7921540..7923960-chr18:7924672..7926506,2	K562	blood:
9	chr18:7581543..7584440-chr18:7588046..7590216,2	K562	blood:
10	chr18:7953033..7955520-chr18:7955662..7957889,2	MCF-7	breast:
11	chr18:7986635..7988175-chr18:7990212..7991772,2	K562	blood:
12	chr18:7560178..7562976-chr18:7564673..7567118,2	MCF-7	breast:
13	chr18:7849859..7852810-chr18:7852966..7855676,3	K562	blood:
14	chr18:8032781..8034914-chr18:8035968..8038793,2	K562	blood:
15	chr18:7675331..7677808-chr18:7679199..7680841,3	K562	blood:
16	chr18:8051019..8052876-chr18:8070132..8072899,2	K562	blood:
17	chr18:7601321..7603533-chr18:7605983..7608690,2	K562	blood:
18	chr18:7606732..7608524-chr18:7612003..7613987,2	K562	blood:
19	chr18:8046800..8049219-chr18:8053263..8054942,2	K562	blood:
20	chr18:8051019..8052876-chr18:8070132..8072899,2	K562	blood:
21	chr18:8084340..8084935-chr18:8094926..8095705,2	K562	blood:
22	chr18:7749744..7751445-chr18:7751627..7754409,2	MCF-7	breast:
23	chr18:7747994..7750042-chr18:7751326..7753624,2	K562	blood:
24	chr18:7755817..7756409-chr5:151977437..151978212,2	MCF-7	breast:
25	chr18:7919128..7921184-chr18:7922798..7925622,2	K562	blood:
26	chr18:7928564..7930698-chr18:7930899..7932884,2	K562	blood:
27	chr18:7601321..7603533-chr18:7605983..7608690,2	K562	blood:
28	chr18:7611758..7613700-chr18:7613892..7616475,3	K562	blood:
29	chr18:8075118..8077188-chr18:8078640..8081116,3	K562	blood:
30	chr18:7850877..7852810-chr18:7852966..7855500,2	K562	blood:
31	chr18:7936902..7939574-chr18:7940048..7941947,2	K562	blood:
32	chr18:8008779..8010342-chr18:8020655..8023577,2	MCF-7	breast:
33	chr18:8008779..8010342-chr18:8020655..8023577,2	MCF-7	breast:
34	chr18:7881362..7883876-chr18:7886190..7888393,2	MCF-7	breast:
35	chr18:7556771..7559463-chr18:7563687..7565562,2	K562	blood:
36	chr18:7849859..7852810-chr18:7852966..7855676,3	K562	blood:
37	chr18:8026329..8028067-chr18:8040720..8043000,2	K562	blood:
38	chr18:7566319..7569036-chr18:7569097..7573393,5	K562	blood:
39	chr18:8032781..8034914-chr18:8035968..8038793,2	K562	blood:
40	chr18:7567923..7568423-chr20:61846958..61847561,2	MCF-7	breast:
41	chr18:7221690..7222309-chr18:7566824..7567430,2	K562	blood:
42	chr18:7745866..7749831-chr18:7752461..7755443,3	MCF-7	breast:
43	chr18:7953033..7955520-chr18:7955662..7957889,2	MCF-7	breast:
44	chr18:8026329..8028067-chr18:8040720..8043000,2	K562	blood:
45	chr18:8052032..8053002-chr18:8389571..8390235,2	MCF-7	breast:
46	chr18:7675475..7677808-chr18:7679199..7680841,2	K562	blood:
47	chr18:7986635..7988175-chr18:7990212..7991772,2	K562	blood:
48	chr18:7561940..7563899-chr18:7566456..7568145,3	K562	blood:
49	chr18:7272078..7272898-chr18:7626542..7627160,2	MCF-7	breast:
50	chr18:7745866..7749831-chr18:7752461..7755443,3	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LAMA1-5	chr18:7749057-7749441	NONHSAT057159
2	lnc-LAMA1-5	chr18:7754762-7754829	ENSG00000266767.1
3	lnc-AP001793.1-9	chr18:7995568-7995782	NONHSAT057163
4	lnc-LAMA1-5	chr18:7740621-7741979	NONHSAT057159
5	lnc-LAMA1-5	chr18:7749057-7749197	ENSG00000266767.1
6	lnc-LAMA1-5	chr18:7751018-7751503	ENSG00000266767.1
7	lnc-LAMA1-5	chr18:7747531-7747656	ENSG00000266767.1
8	lnc-LAMA1-5	chr18:7749057-7749441	ENSG00000266767.1
9	lnc-LAMA1-5	chr18:7741308-7741979	ENSG00000266767.1
10	lnc-LRRC30-4	chr18:7814116-7815728	ENSG00000264596.1

No data

Variant related genes	Relation type
ENSG00000266767	TF binding region
ENSG00000264596	TF binding region
PTPRM	TF binding region
ENSG00000263827	TF binding region
ENSG00000199856	TF binding region
ENSG00000221631	TF binding region
ENSG00000266767	CpG island
ENSG00000264596	CpG island
PTPRM	CpG island
ENSG00000263827	CpG island
ENSG00000199856	CpG island
ENSG00000221631	CpG island
ENSG00000266767	chromatin interactions
ENSG00000173482	chromatin interactions
ENSG00000149658	chromatin interactions

Extended variants
information (count: 19483 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:19483 , 50 per page) page: 1 2 3 4 5 6 7 ... 390

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577677919	chr18:7562003-7562004	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs567092527	chr18:7562026-7562027	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs368815682	chr18:7562059-7562060	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs143920852	chr18:7562067-7562068	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs185926411	chr18:7562093-7562094	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs563293346	chr18:7562157-7562158	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs16952140	chr18:7562188-7562189	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs146867441	chr18:7562191-7562192	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs149035206	chr18:7562199-7562200	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs555542734	chr18:7562241-7562242	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs529451299	chr18:7562247-7562248	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs143002753	chr18:7562252-7562253	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs571487783	chr18:7562282-7562283	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs58953090	chr18:7562317-7562318	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs116893516	chr18:7562330-7562331	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs567259649	chr18:7562340-7562341	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs535914040	chr18:7562375-7562376	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs73385357	chr18:7562397-7562398	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs189337005	chr18:7562401-7562402	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs113651368	chr18:7562466-7562467	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs78852401	chr18:7562526-7562527	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs557739279	chr18:7562582-7562583	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs556677379	chr18:7562598-7562599	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs561711395	chr18:7562709-7562710	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs577821816	chr18:7562713-7562714	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs375743713	chr18:7562741-7562742	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs577728980	chr18:7562783-7562784	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs182387328	chr18:7562875-7562876	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs557074818	chr18:7562890-7562891	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs573696009	chr18:7562915-7562916	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs542685328	chr18:7562927-7562928	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs371622419	chr18:7562934-7562935	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs559582838	chr18:7562937-7562938	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs528346521	chr18:7562985-7562986	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs545291084	chr18:7562994-7562995	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs571261180	chr18:7563059-7563060	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs534074725	chr18:7563101-7563102	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs565031155	chr18:7563130-7563131	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs530765389	chr18:7563131-7563132	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs373755908	chr18:7563173-7563174	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs140236926	chr18:7563174-7563175	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs567395820	chr18:7563198-7563199	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs529674055	chr18:7563207-7563208	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs186539601	chr18:7563350-7563351	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs191092364	chr18:7563382-7563383	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs566487588	chr18:7563396-7563397	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs534963130	chr18:7563427-7563428	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs369174589	chr18:7563436-7563437	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs367561504	chr18:7563495-7563496	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs146953196	chr18:7563743-7563744	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
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
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
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Breast cancer	17133270	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Schizophrenia	20838587	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:7933 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:7558200-7562000	Weak transcription	Spleen	Spleen
2	chr18:7558200-7566000	Weak transcription	Right Atrium	heart
3	chr18:7560200-7564600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr18:7560200-7565200	Weak transcription	Psoas Muscle	Psoas
5	chr18:7560200-7566200	Weak transcription	Fetal Muscle Trunk	muscle
6	chr18:7560400-7565200	Weak transcription	Left Ventricle	heart
7	chr18:7560400-7566000	Weak transcription	Lung	lung
8	chr18:7560400-7566000	Weak transcription	Pancreas	Pancrea
9	chr18:7560800-7562200	Enhancers	Fetal Thymus	thymus
10	chr18:7561400-7562400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr18:7561600-7562200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr18:7561600-7562200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr18:7561600-7562200	Enhancers	Brain Cingulate Gyrus	brain
14	chr18:7561600-7562200	Enhancers	Fetal Stomach	stomach
15	chr18:7561600-7562600	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr18:7561600-7562600	Enhancers	HepG2	liver
17	chr18:7561600-7562800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr18:7561600-7562800	Enhancers	HUVEC	blood vessel
19	chr18:7561600-7565600	Enhancers	Colon Smooth Muscle	Colon
20	chr18:7561800-7562000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr18:7561800-7562000	Enhancers	Thymus	Thymus
22	chr18:7561800-7562200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr18:7561800-7562200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr18:7561800-7562200	Enhancers	Brain Angular Gyrus	brain
25	chr18:7561800-7562400	Enhancers	H1 Cell Line	embryonic stem cell
26	chr18:7561800-7562400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr18:7561800-7562400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr18:7561800-7562600	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr18:7561800-7562600	Enhancers	H9 Cell Line	embryonic stem cell
30	chr18:7561800-7562800	Enhancers	Adipose Nuclei	Adipose
31	chr18:7561800-7562800	Enhancers	Brain Anterior Caudate	brain
32	chr18:7561800-7563200	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr18:7561800-7563200	Enhancers	Rectal Smooth Muscle	rectum
34	chr18:7562000-7562200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr18:7562000-7562200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr18:7562000-7562200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr18:7562000-7562200	Enhancers	Right Ventricle	heart
38	chr18:7562000-7562200	Enhancers	Spleen	Spleen
39	chr18:7562000-7562400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr18:7562000-7562400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr18:7562000-7562400	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr18:7562000-7562400	Enhancers	Brain Hippocampus Middle	brain
43	chr18:7562000-7562400	Enhancers	Brain Substantia Nigra	brain
44	chr18:7562000-7562400	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr18:7562000-7562600	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr18:7562000-7562600	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr18:7562000-7562600	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr18:7562000-7562800	Enhancers	Fetal Heart	heart
49	chr18:7562000-7563200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr18:7562000-7564400	Weak transcription	Thymus	Thymus

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