Variant report

Variant	nsv911285
Chromosome Location	chr19:18646932-18667472
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:720)
CpG islands
(count:733)
Chromatin interactive
region (count:46)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:720 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:18654723-18655389	K562	blood:	n/a	n/a
2	ARID3A	chr19:18662903-18662993	K562	blood:	n/a	n/a
3	ATF1	chr19:18654709-18655209	K562	blood:	n/a	n/a
4	ATF2	chr19:18654720-18655068	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr19:18654677-18655190	GM12878	blood:	n/a	n/a
6	ATF3	chr19:18654747-18655106	K562	blood:	n/a	n/a
7	BCL3	chr19:18654653-18655249	K562	blood:	n/a	n/a
8	BCLAF1	chr19:18654639-18655145	GM12878	blood:	n/a	n/a
9	BCLAF1	chr19:18654617-18655225	K562	blood:	n/a	n/a
10	BCLAF1	chr19:18654656-18655175	K562	blood:	n/a	n/a
11	BHLHE40	chr19:18653849-18653869	K562	blood:	n/a	n/a
12	BHLHE40	chr19:18654660-18655082	GM12878	blood:	n/a	n/a
13	BHLHE40	chr19:18655805-18655820	HepG2	liver:	n/a	n/a
14	BHLHE40	chr19:18653850-18654041	GM12878	blood:	n/a	chr19:18653936-18653952
15	BHLHE40	chr19:18654701-18655935	K562	blood:	n/a	n/a
16	BRCA1	chr19:18654814-18655014	GM12878	blood:	n/a	n/a
17	CBX3	chr19:18654619-18655458	K562	blood:	n/a	n/a
18	CBX3	chr19:18654720-18655204	K562	blood:	n/a	n/a
19	CCNT2	chr19:18653932-18653960	K562	blood:	n/a	n/a
20	CCNT2	chr19:18654368-18655218	K562	blood:	n/a	chr19:18654390-18654399 chr19:18655020-18655040
21	CCNT2	chr19:18648532-18648636	K562	blood:	n/a	n/a
22	CEBPB	chr19:18654663-18655942	K562	blood:	n/a	chr19:18655618-18655629
23	CEBPB	chr19:18654839-18655780	K562	blood:	n/a	chr19:18655618-18655629
24	CEBPB	chr19:18665182-18665242	A549	lung:	n/a	chr19:18665217-18665228
25	CEBPB	chr19:18665116-18665376	HepG2	liver:	n/a	chr19:18665217-18665228
26	CEBPB	chr19:18655566-18655713	A549	lung:	n/a	chr19:18655618-18655629
27	CEBPB	chr19:18659036-18659255	HepG2	liver:	n/a	chr19:18659152-18659163
28	CEBPB	chr19:18665169-18665323	IMR90	lung:	n/a	chr19:18665217-18665228
29	CEBPB	chr19:18659218-18659230	K562	blood:	n/a	n/a
30	CEBPB	chr19:18656270-18656516	K562	blood:	n/a	n/a
31	CEBPB	chr19:18659148-18659209	IMR90	lung:	n/a	chr19:18659152-18659163
32	CEBPB	chr19:18655566-18655732	HepG2	liver:	n/a	chr19:18655618-18655629
33	CEBPD	chr19:18654164-18654632	HepG2	liver:	n/a	n/a
34	CEBPD	chr19:18654642-18655360	K562	blood:	n/a	n/a
35	CEBPD	chr19:18654573-18655402	K562	blood:	n/a	n/a
36	CHD1	chr19:18654665-18655129	GM12878	blood:	n/a	n/a
37	CHD2	chr19:18653887-18653997	GM12878	blood:	n/a	n/a
38	CHD2	chr19:18653579-18653616	GM12878	blood:	n/a	n/a
39	CHD2	chr19:18654243-18655137	K562	blood:	n/a	n/a
40	CHD2	chr19:18654222-18655118	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr19:18654203-18655183	GM12878	blood:	n/a	n/a
42	CHD2	chr19:18654261-18655073	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr19:18654303-18654534	HepG2	liver:	n/a	n/a
44	CREB1	chr19:18654174-18655309	K562	blood:	n/a	n/a
45	CREB1	chr19:18653722-18655186	GM12878	blood:	n/a	n/a
46	CREB1	chr19:18654184-18654531	A549	lung:	n/a	n/a
47	CREB1	chr19:18654732-18655071	A549	lung:	n/a	n/a
48	CTCF	chr19:18654865-18655049	LNCaP	prostate:	n/a	n/a
49	CTCF	chr19:18654880-18655030	HMEC	breast:	n/a	n/a
50	CTCF	chr19:18654860-18655010	NHEK	skin:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:18667414-18667464	LNCaP	prostate:	n/a
2	chr19:18667414-18667464	LNCaP	prostate:	n/a
3	chr19:18654267-18654317	Jurkat	blood:	n/a
4	chr19:18657397-18657447	PFSK-1	brain:	n/a
5	chr19:18654681-18654731	U87	brain:	n/a
6	chr19:18654267-18654317	PANC-1	pancreas:	n/a
7	chr19:18667414-18667464	GM06990	blood:	n/a
8	chr19:18654681-18654731	HCPEpiC	choroid plexus:	n/a
9	chr19:18650416-18650466	ECC-1	luminal epithelium:	n/a
10	chr19:18667414-18667464	ProgFib	skin:	n/a
11	chr19:18654267-18654317	CMK	blood:	n/a
12	chr19:18654433-18654483	AG04449	skin:	fetal
13	chr19:18654361-18654411	SKMC	muscle:	n/a
14	chr19:18652534-18652584	SK-N-SH	brain:	n/a
15	chr19:18654361-18654411	HCPEpiC	choroid plexus:	n/a
16	chr19:18652534-18652584	AG04450	lung:	fetal
17	chr19:18653918-18653968	GM12891	blood:	n/a
18	chr19:18667414-18667464	Jurkat	blood:	n/a
19	chr19:18667414-18667464	NB4	blood:	n/a
20	chr19:18657397-18657447	HCF	heart:	n/a
21	chr19:18654267-18654317	HNPCEpiC	eye:	n/a
22	chr19:18654548-18654598	GM12891	blood:	n/a
23	chr19:18654548-18654598	AG10803	skin:	n/a
24	chr19:18654681-18654731	HEEpiC	esophagus:	n/a
25	chr19:18652534-18652584	GM12891	blood:	n/a
26	chr19:18664479-18664529	T-47D	breast:	n/a
27	chr19:18650416-18650466	NH-A	brain:	n/a
28	chr19:18652534-18652584	SK-N-SH_RA	brain:	n/a
29	chr19:18653918-18653968	HMEC	breast:	n/a
30	chr19:18654267-18654317	Caco-2	colon:	n/a
31	chr19:18657397-18657447	AG04450	lung:	fetal
32	chr19:18654681-18654731	HAEpiC	amniotic membrane:	n/a
33	chr19:18652534-18652584	GM19239	blood:	n/a
34	chr19:18654433-18654483	IMR90	lung:	fetal
35	chr19:18657397-18657447	BJ	skin:	n/a
36	chr19:18664479-18664529	HL-60	blood:	n/a
37	chr19:18654681-18654731	ovcar-3	ovarian:	n/a
38	chr19:18654267-18654317	HUVEC	blood vessel:	n/a
39	chr19:18650416-18650466	HCF	heart:	n/a
40	chr19:18653918-18653968	A549	lung:	n/a
41	chr19:18650416-18650466	Hela-S3	cervix:	n/a
42	chr19:18654433-18654483	HMEC	breast:	n/a
43	chr19:18654681-18654731	AG10803	skin:	n/a
44	chr19:18654949-18654999	Hela-S3	cervix:	n/a
45	chr19:18654548-18654598	AG04450	lung:	fetal
46	chr19:18652534-18652584	NHBE	bronchial:	n/a
47	chr19:18654548-18654598	HMEC	breast:	n/a
48	chr19:18653918-18653968	NHDF-neo	bronchial:	n/a
49	chr19:18654267-18654317	MCF10A-Er-Src	breast:	n/a
50	chr19:18657397-18657447	HRCEpiC	kidney:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:18653032..18656930-chr19:18667045..18670995,8	MCF-7	breast:
2	chr19:18650801..18653024-chr19:18671456..18674102,2	K562	blood:
3	chr19:18662721..18665534-chr19:18665875..18667886,2	MCF-7	breast:
4	chr19:18631459..18633367-chr19:18667345..18670376,4	K562	blood:
5	chr19:18667097..18671007-chr19:18677068..18684435,17	K562	blood:
6	chr19:18633341..18635579-chr19:18650519..18652255,2	K562	blood:
7	chr19:18640357..18642464-chr19:18650908..18653787,2	MCF-7	breast:
8	chr19:18653590..18656982-chr19:18704077..18706738,3	K562	blood:
9	chr19:18667076..18669031-chr19:18699935..18702117,2	K562	blood:
10	chr19:18643276..18646755-chr19:18646873..18650377,4	K562	blood:
11	chr19:18653459..18656385-chr19:18699225..18703130,9	K562	blood:
12	chr19:18653476..18656385-chr19:18700159..18703130,5	K562	blood:
13	chr19:18666965..18674770-chr19:18676405..18685095,25	K562	blood:
14	chr19:18653032..18656930-chr19:18667045..18670995,8	MCF-7	breast:
15	chr19:18630548..18633267-chr19:18667345..18670044,3	K562	blood:
16	chr19:18646844..18649576-chr19:18650784..18652699,2	MCF-7	breast:
17	chr19:18651498..18655648-chr19:18680777..18683781,5	MCF-7	breast:
18	chr19:18648889..18650815-chr19:18652717..18655388,4	K562	blood:
19	chr19:18630875..18635401-chr19:18651200..18655863,9	MCF-7	breast:
20	chr19:18641022..18643791-chr19:18650556..18652097,2	MCF-7	breast:
21	chr19:18666281..18667937-chr19:18697239..18698916,2	K562	blood:
22	chr19:18648889..18650815-chr19:18652717..18655388,4	K562	blood:
23	chr19:18666812..18670172-chr19:18680715..18684041,6	MCF-7	breast:
24	chr19:18652388..18655450-chr19:18667016..18670630,4	K562	blood:
25	chr19:18649378..18653671-chr19:18667425..18670328,5	MCF-7	breast:
26	chr19:18651018..18652538-chr19:18681484..18683869,2	K562	blood:
27	chr19:18667424..18670168-chr19:18699281..18701481,3	MCF-7	breast:
28	chr19:18629917..18634196-chr19:18652150..18655589,5	MCF-7	breast:
29	chr19:18653470..18656783-chr19:18680897..18684291,6	K562	blood:
30	chr19:18642522..18644970-chr19:18651017..18653848,4	K562	blood:
31	chr19:18662721..18665534-chr19:18665875..18667886,2	MCF-7	breast:
32	chr19:18652388..18655450-chr19:18667016..18670630,4	K562	blood:
33	chr19:18536175..18537815-chr19:18653605..18655763,2	MCF-7	breast:
34	chr19:18653886..18656782-chr19:18668675..18670368,2	MCF-7	breast:
35	chr19:18629748..18634724-chr19:18652806..18658264,15	K562	blood:
36	chr19:18629876..18632922-chr19:18647804..18650314,4	MCF-7	breast:
37	chr19:18630485..18634839-chr19:18666846..18671916,7	MCF-7	breast:
38	chr19:18653777..18655402-chr19:18661195..18662845,2	MCF-7	breast:
39	chr19:18631281..18633201-chr19:18647451..18649167,2	K562	blood:
40	chr19:18645533..18647527-chr19:18689802..18691747,2	K562	blood:
41	chr19:18646831..18648378-chr19:18653239..18655225,2	MCF-7	breast:
42	chr19:18649378..18653671-chr19:18667425..18670328,5	MCF-7	breast:
43	chr19:18632726..18634686-chr19:18649463..18652079,3	MCF-7	breast:
44	chr19:18629959..18634840-chr19:18652830..18656407,13	K562	blood:
45	chr19:18651038..18656783-chr19:18680897..18685521,14	K562	blood:
46	chr19:18652388..18654838-chr19:18668474..18670630,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KXD1-2	chr19:18646796-18646998	ENSG00000269191.1

No data

Variant related genes	Relation type
FKBP8	TF binding region
KXD1	TF binding region
FKBP8	CpG island
KXD1	CpG island
ENSG00000006016	chromatin interactions
ENSG00000269191	chromatin interactions
ENSG00000006015	chromatin interactions
ENSG00000268938	chromatin interactions
ENSG00000105656	chromatin interactions
ENSG00000105700	chromatin interactions
ENSG00000268983	chromatin interactions
ENSG00000105701	chromatin interactions
ENSG00000221983	chromatin interactions
ENSG00000268030	chromatin interactions
ENSG00000130511	chromatin interactions

Extended variants
information (count: 926 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:926 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8104439	chr19:18646932-18646933	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs117472330	chr19:18646933-18646934	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs58604797	chr19:18647033-18647034	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs377319682	chr19:18647053-18647054	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs562004971	chr19:18647077-18647078	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs181883288	chr19:18647101-18647102	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs550169043	chr19:18647128-18647129	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs563686414	chr19:18647139-18647140	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs148873690	chr19:18647140-18647141	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs562452556	chr19:18647143-18647144	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs552418545	chr19:18647144-18647145	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs553625157	chr19:18647187-18647188	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs566259522	chr19:18647194-18647195	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs118113459	chr19:18647208-18647209	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs71336682	chr19:18647209-18647210	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs71336683	chr19:18647215-18647216	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs548384782	chr19:18647224-18647225	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs568368870	chr19:18647250-18647251	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs11574811	chr19:18647261-18647262	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs186088872	chr19:18647377-18647378	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs576801018	chr19:18647379-18647380	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs544411310	chr19:18647423-18647424	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs552841634	chr19:18647435-18647436	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs190387639	chr19:18647518-18647519	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs181713517	chr19:18647534-18647535	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs532887805	chr19:18647535-18647536	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs555620389	chr19:18647566-18647567	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs575573360	chr19:18647580-18647581	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs544548791	chr19:18647637-18647638	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs143626141	chr19:18647644-18647645	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs560717671	chr19:18647648-18647649	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs6512273	chr19:18647664-18647665	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs559546479	chr19:18647696-18647697	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs377534486	chr19:18647712-18647713	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs548347870	chr19:18647717-18647718	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs148054406	chr19:18647738-18647739	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs142387681	chr19:18647739-18647740	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs112695485	chr19:18647748-18647749	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs550894077	chr19:18647807-18647808	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs144612970	chr19:18647871-18647872	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs138513933	chr19:18647876-18647877	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs141641362	chr19:18647920-18647921	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs150734598	chr19:18647963-18647964	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs374699810	chr19:18648003-18648004	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs35065930	chr19:18648009-18648010	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs35767830	chr19:18648040-18648041	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs113736240	chr19:18648075-18648076	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs376810279	chr19:18648126-18648127	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs555583584	chr19:18648127-18648128	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs575534841	chr19:18648131-18648132	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Follicular lymphoma	20505157	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	20179077	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Lung cancer	17297452	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Chordoma	18071362	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21364760	CNVD
Mycobacterial infection	18421352	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute monocytic leukemia	16498392	CNVD
Lung cancer	18438408	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Liver carcinoma	19366792	CNVD
Colorectal cancer	19455253	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Cancer	17440070	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:870 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18632800-18652200	Weak transcription	Fetal Heart	heart
2	chr19:18632800-18652800	Weak transcription	Stomach Mucosa	stomach
3	chr19:18632800-18654600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr19:18633000-18653400	Weak transcription	Psoas Muscle	Psoas
5	chr19:18633200-18653200	Weak transcription	Right Atrium	heart
6	chr19:18633800-18648600	Weak transcription	A549	lung
7	chr19:18633800-18652400	Weak transcription	Fetal Brain Male	brain
8	chr19:18633800-18652800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr19:18633800-18653400	Weak transcription	Fetal Kidney	kidney
10	chr19:18634000-18651800	Weak transcription	Hela-S3	cervix
11	chr19:18634000-18652200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr19:18637600-18648200	Weak transcription	K562	blood
13	chr19:18638600-18650800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr19:18640400-18652000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr19:18640400-18652200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr19:18641800-18652400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr19:18641800-18652800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
18	chr19:18641800-18653000	Strong transcription	Fetal Stomach	stomach
19	chr19:18642000-18648800	Strong transcription	Placenta	Placenta
20	chr19:18642000-18652000	Strong transcription	Primary neutrophils fromperipheralblood	blood
21	chr19:18642000-18652400	Strong transcription	Fetal Muscle Leg	muscle
22	chr19:18642000-18652600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr19:18642000-18652600	Strong transcription	Brain Hippocampus Middle	brain
24	chr19:18642000-18652800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr19:18642000-18652800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr19:18642000-18652800	Strong transcription	Fetal Intestine Small	intestine
27	chr19:18642200-18648000	Strong transcription	Liver	Liver
28	chr19:18642200-18649000	Strong transcription	Primary T helper cells PMA-I stimulated	--
29	chr19:18642200-18650000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr19:18642200-18651800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr19:18642200-18652000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr19:18642200-18652200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr19:18642200-18652200	Strong transcription	Fetal Muscle Trunk	muscle
34	chr19:18642200-18652200	Strong transcription	Stomach Smooth Muscle	stomach
35	chr19:18642200-18652400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr19:18642200-18652400	Strong transcription	Gastric	stomach
37	chr19:18642200-18652400	Strong transcription	Thymus	Thymus
38	chr19:18642200-18652400	Strong transcription	NHLF	lung
39	chr19:18642200-18652600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
40	chr19:18642200-18652600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr19:18642200-18652600	Strong transcription	Primary T cells from cord blood	blood
42	chr19:18642200-18652600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr19:18642200-18652600	Strong transcription	Cortex derived primary cultured neurospheres	brain
44	chr19:18642200-18652600	Strong transcription	Esophagus	oesophagus
45	chr19:18642200-18652600	Strong transcription	Fetal Intestine Large	intestine
46	chr19:18642200-18652600	Strong transcription	Ovary	ovary
47	chr19:18642200-18652800	Strong transcription	Primary monocytes fromperipheralblood	blood
48	chr19:18642200-18652800	Strong transcription	Fetal Thymus	thymus
49	chr19:18642200-18653000	Strong transcription	HUES64 Cell Line	embryonic stem cell
50	chr19:18642400-18650600	Weak transcription	NH-A	brain

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