Variant report

Variant	nsv911234
Chromosome Location	chr19:18075807-18128388
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2225)
CpG islands
(count:3055)
Chromatin interactive
region (count:153)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2225 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:18124583-18124832	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:18120128-18120420	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:18117859-18118033	K562	blood:	n/a	n/a
4	ARID3A	chr19:18117886-18118134	HepG2	liver:	n/a	n/a
5	ARID3A	chr19:18080759-18081106	K562	blood:	n/a	n/a
6	ATF1	chr19:18110455-18111046	K562	blood:	n/a	n/a
7	ATF1	chr19:18118860-18119087	K562	blood:	n/a	n/a
8	ATF1	chr19:18080804-18081177	K562	blood:	n/a	n/a
9	ATF1	chr19:18096285-18096573	K562	blood:	n/a	n/a
10	ATF1	chr19:18124524-18124832	K562	blood:	n/a	n/a
11	ATF2	chr19:18117738-18118178	GM12878	blood:	n/a	n/a
12	ATF2	chr19:18117757-18118190	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr19:18112254-18112606	GM12878	blood:	n/a	n/a
14	ATF2	chr19:18117706-18118130	GM12878	blood:	n/a	n/a
15	ATF2	chr19:18107610-18108002	GM12878	blood:	n/a	n/a
16	ATF3	chr19:18118855-18119083	K562	blood:	n/a	chr19:18119009-18119023 chr19:18118970-18118979 chr19:18118904-18118913
17	ATF3	chr19:18111778-18112037	K562	blood:	n/a	n/a
18	ATF3	chr19:18124474-18124867	K562	blood:	n/a	n/a
19	BACH1	chr19:18109300-18109354	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr19:18107609-18107921	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr19:18110499-18110924	K562	blood:	n/a	n/a
22	BACH1	chr19:18118715-18118862	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr19:18080611-18080993	K562	blood:	n/a	n/a
24	BACH1	chr19:18111999-18112161	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr19:18117749-18118216	H1-hESC	embryonic stem cell:	n/a	n/a
26	BCL3	chr19:18112301-18112727	A549	lung:	n/a	chr19:18112501-18112510 chr19:18112502-18112511 chr19:18112397-18112406
27	BCL3	chr19:18111795-18112156	A549	lung:	n/a	n/a
28	BCL3	chr19:18111746-18112146	A549	lung:	n/a	chr19:18111792-18111801
29	BCL3	chr19:18117704-18118246	A549	lung:	n/a	n/a
30	BCLAF1	chr19:18107516-18108049	GM12878	blood:	n/a	n/a
31	BCLAF1	chr19:18118875-18119264	GM12878	blood:	n/a	chr19:18118933-18118946
32	BCLAF1	chr19:18107531-18107989	GM12878	blood:	n/a	n/a
33	BCLAF1	chr19:18111751-18112236	GM12878	blood:	n/a	chr19:18111792-18111801
34	BHLHE40	chr19:18111693-18112210	GM12878	blood:	n/a	n/a
35	BHLHE40	chr19:18110443-18110828	K562	blood:	n/a	n/a
36	BHLHE40	chr19:18111744-18112288	K562	blood:	n/a	n/a
37	BHLHE40	chr19:18096320-18096509	K562	blood:	n/a	n/a
38	BHLHE40	chr19:18111767-18111988	A549	lung:	n/a	n/a
39	BHLHE40	chr19:18099175-18099344	HepG2	liver:	n/a	n/a
40	BHLHE40	chr19:18107654-18107924	GM12878	blood:	n/a	n/a
41	BHLHE40	chr19:18080784-18081107	K562	blood:	n/a	n/a
42	BHLHE40	chr19:18113438-18113485	GM12878	blood:	n/a	n/a
43	BHLHE40	chr19:18117686-18118228	GM12878	blood:	n/a	n/a
44	BHLHE40	chr19:18111814-18112050	HepG2	liver:	n/a	n/a
45	BHLHE40	chr19:18117696-18118098	K562	blood:	n/a	n/a
46	BHLHE40	chr19:18107696-18107973	K562	blood:	n/a	n/a
47	BRCA1	chr19:18108648-18109540	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr19:18111526-18112043	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr19:18108040-18108126	GM12878	blood:	n/a	n/a
50	BRCA1	chr19:18117937-18117989	HepG2	liver:	n/a	n/a

(count:3055 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:18111880-18111930	T-47D	breast:	n/a
2	chr19:18118298-18118348	NHDF-neo	bronchial:	n/a
3	chr19:18124823-18124873	SK-N-SH_RA	brain:	n/a
4	chr19:18113604-18113654	K562	blood:	n/a
5	chr19:18085190-18085240	IMR90	lung:	fetal
6	chr19:18111880-18111930	T-47D	breast:	n/a
7	chr19:18118298-18118348	NHDF-neo	bronchial:	n/a
8	chr19:18124823-18124873	SK-N-SH_RA	brain:	n/a
9	chr19:18113604-18113654	K562	blood:	n/a
10	chr19:18085190-18085240	IMR90	lung:	fetal
11	chr19:18111389-18111439	HL-60	blood:	n/a
12	chr19:18113604-18113654	HMEC	breast:	n/a
13	chr19:18120692-18120742	U87	brain:	n/a
14	chr19:18113585-18113635	HEEpiC	esophagus:	n/a
15	chr19:18085190-18085240	SKMC	muscle:	n/a
16	chr19:18085190-18085240	ovcar-3	ovarian:	n/a
17	chr19:18119847-18119897	NB4	blood:	n/a
18	chr19:18120614-18120664	HCT-116	colon:	n/a
19	chr19:18120614-18120664	GM19239	blood:	n/a
20	chr19:18109484-18109534	HAEpiC	amniotic membrane:	n/a
21	chr19:18107778-18107828	HCF	heart:	n/a
22	chr19:18118880-18118930	HPAEpiC	pulmonary alveolar:	n/a
23	chr19:18111739-18111789	CMK	blood:	n/a
24	chr19:18111739-18111789	NHDF-neo	bronchial:	n/a
25	chr19:18092572-18092622	AG09309	skin:	n/a
26	chr19:18092572-18092622	PANC-1	pancreas:	n/a
27	chr19:18109484-18109534	HepG2	liver:	n/a
28	chr19:18112433-18112483	HUVEC	blood vessel:	n/a
29	chr19:18118835-18118885	ovcar-3	ovarian:	n/a
30	chr19:18118835-18118885	BE2_C	brain:	n/a
31	chr19:18119847-18119897	MCF-7	breast:	n/a
32	chr19:18120692-18120742	AG09319	gingival:	n/a
33	chr19:18120614-18120664	AG09309	skin:	n/a
34	chr19:18078973-18079023	CMK	blood:	n/a
35	chr19:18120626-18120676	BJ	skin:	n/a
36	chr19:18084497-18084547	ovcar-3	ovarian:	n/a
37	chr19:18118298-18118348	SK-N-SH_RA	brain:	n/a
38	chr19:18096662-18096712	PANC-1	pancreas:	n/a
39	chr19:18112042-18112092	NHBE	bronchial:	n/a
40	chr19:18084497-18084547	AG10803	skin:	n/a
41	chr19:18091245-18091295	MCF-7	breast:	n/a
42	chr19:18120819-18120869	PrEC	prostate:	n/a
43	chr19:18109226-18109276	PANC-1	pancreas:	n/a
44	chr19:18088495-18088545	GM19239	blood:	n/a
45	chr19:18093867-18093917	A549	lung:	n/a
46	chr19:18120614-18120664	ECC-1	luminal epithelium:	n/a
47	chr19:18077791-18077841	Hela-S3	cervix:	n/a
48	chr19:18091245-18091295	GM19239	blood:	n/a
49	chr19:18108895-18108945	U87	brain:	n/a
50	chr19:18120614-18120664	Hela-S3	cervix:	n/a

(count:153 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr19:18120097..18121750-chr19:18126783..18129067,2	K562	blood:
2	chr19:18108317..18109305-chr5:172385880..172386657,2	HCT-116	colon:
3	chr19:18075092..18076016-chr19:18107540..18108277,2	MCF-7	breast:
4	chr19:18053806..18056439-chr19:18107928..18110413,2	MCF-7	breast:
5	chr19:18097326..18100602-chr19:18101785..18105013,3	K562	blood:
6	chr19:17972756..17976399-chr19:18110401..18113176,4	MCF-7	breast:
7	chr19:17980895..17981784-chr19:18107576..18108251,2	MCF-7	breast:
8	chr19:18116377..18117919-chr19:18196385..18197944,2	K562	blood:
9	chr19:17977046..17979867-chr19:18087845..18090111,2	K562	blood:
10	chr19:18107780..18110414-chr19:18220560..18222178,2	MCF-7	breast:
11	chr19:18076276..18077913-chr19:18085096..18087175,2	K562	blood:
12	chr19:18068202..18071106-chr19:18109309..18111194,2	MCF-7	breast:
13	chr19:18045893..18048560-chr19:18097905..18100240,2	K562	blood:
14	chr19:18044248..18046131-chr19:18107808..18109539,3	MCF-7	breast:
15	chr19:18056861..18058558-chr19:18107372..18108294,7	K562	blood:
16	chr19:18085605..18088089-chr19:18094950..18097092,2	K562	blood:
17	chr19:17982249..17983850-chr19:18081596..18084484,2	K562	blood:
18	chr19:18111363..18113248-chr19:18391327..18393546,2	MCF-7	breast:
19	chr19:18110122..18111942-chr19:18122716..18124889,2	K562	blood:
20	chr19:18118081..18123084-chr19:18129890..18134974,7	K562	blood:
21	chr19:18055988..18065489-chr19:18073307..18083163,16	K562	blood:
22	chr19:18102561..18105389-chr19:18108645..18110654,2	MCF-7	breast:
23	chr19:18118535..18121837-chr19:18124843..18129099,4	MCF-7	breast:
24	chr19:18061398..18062926-chr19:18110709..18112847,2	MCF-7	breast:
25	chr19:17972652..17976258-chr19:18108249..18111940,3	K562	blood:
26	chr19:18076868..18079514-chr19:18090514..18092677,2	K562	blood:
27	chr19:18116541..18118354-chr19:18390841..18393418,2	MCF-7	breast:
28	chr19:18111522..18113675-chr19:18263601..18266020,2	MCF-7	breast:
29	chr19:17970326..17972739-chr19:18109182..18113129,4	MCF-7	breast:
30	chr19:18080070..18081745-chr19:18084699..18086287,2	K562	blood:
31	chr19:17969000..17971392-chr19:18094400..18097234,2	K562	blood:
32	chr19:18108637..18109581-chr19:18168824..18169425,2	K562	blood:
33	chr19:18042015..18046361-chr19:18110121..18114952,6	K562	blood:
34	chr19:10305089..10305816-chr19:18111357..18112197,2	Hela-S3	cervix:
35	chr19:18092395..18094277-chr19:18107509..18109156,2	K562	blood:
36	chr19:18055450..18057221-chr19:18107817..18109855,2	MCF-7	breast:
37	chr19:18111944..18112857-chr3:195163058..195163777,2	Hela-S3	cervix:
38	chr19:18043847..18045910-chr19:18088508..18091072,2	K562	blood:
39	chr19:18127207..18130221-chr19:18130830..18133295,3	MCF-7	breast:
40	chr19:18109187..18111350-chr19:18263513..18265393,2	K562	blood:
41	chr19:18110960..18114857-chr19:18116339..18121671,9	K562	blood:
42	chr19:18076632..18080569-chr19:18093653..18095894,3	K562	blood:
43	chr19:18111051..18113272-chr19:18901611..18904539,2	MCF-7	breast:
44	chr19:18075042..18077654-chr19:18108302..18110498,2	MCF-7	breast:
45	chr19:17974128..17976258-chr19:18109217..18111940,2	K562	blood:
46	chr19:18111588..18112378-chr6:2765382..2766188,2	Hela-S3	cervix:
47	chr19:18041699..18046361-chr19:18102741..18114952,16	K562	blood:
48	chr19:18123336..18125984-chr19:18263954..18266028,2	MCF-7	breast:
49	chr19:18077567..18079811-chr19:18082377..18085090,2	K562	blood:
50	chr19:18109211..18109917-chr3:156877498..156878394,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL12RB1-2	chr19:18122108-18122312	NONHSAT062932

No data

Variant related genes	Relation type
ENSG00000268032	TF binding region
RNA5SP468	TF binding region
KCNN1	TF binding region
ARRDC2	TF binding region
ENSG00000268032	CpG island
RNA5SP468	CpG island
KCNN1	CpG island
ARRDC2	CpG island
ENSG00000196118	chromatin interactions
ENSG00000114331	chromatin interactions
ENSG00000099308	chromatin interactions
ENSG00000163660	chromatin interactions
ENSG00000162783	chromatin interactions
ENSG00000105643	chromatin interactions
ENSG00000207166	chromatin interactions
ENSG00000105640	chromatin interactions
ENSG00000105647	chromatin interactions
ENSG00000268173	chromatin interactions
ENSG00000204388	chromatin interactions
ENSG00000105642	chromatin interactions
ENSG00000105664	chromatin interactions
ENSG00000112237	chromatin interactions
ENSG00000236287	chromatin interactions
ENSG00000268032	chromatin interactions
ENSG00000272017	chromatin interactions
ENSG00000130816	chromatin interactions
ENSG00000135040	chromatin interactions
ENSG00000252591	chromatin interactions
ENSG00000128016	chromatin interactions
ENSG00000100883	chromatin interactions
ENSG00000096996	chromatin interactions
ENSG00000037241	chromatin interactions
ENSG00000181704	chromatin interactions
ENSG00000105641	chromatin interactions
ENSG00000103549	chromatin interactions
ENSG00000007080	chromatin interactions
ENSG00000267959	chromatin interactions
ENSG00000124535	chromatin interactions
ENSG00000204758	chromatin interactions
ENSG00000130522	chromatin interactions

Extended variants
information (count: 2285 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:2285 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7254547	chr19:18075807-18075808	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569875493	chr19:18075823-18075824	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs566857786	chr19:18075849-18075850	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs541954528	chr19:18075911-18075912	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs191006281	chr19:18075946-18075947	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs530541566	chr19:18075947-18075948	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs183875984	chr19:18075949-18075950	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs563909267	chr19:18075970-18075971	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs371017045	chr19:18075974-18075975	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs111393232	chr19:18075975-18075976	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs558811114	chr19:18076008-18076009	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs566735340	chr19:18076038-18076039	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs572485685	chr19:18076065-18076066	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs35697588	chr19:18076074-18076075	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs373369625	chr19:18076081-18076082	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs35151160	chr19:18076082-18076083	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs541107419	chr19:18076102-18076103	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs76753343	chr19:18076106-18076107	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs76622968	chr19:18076109-18076110	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs112222591	chr19:18076192-18076193	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs140980197	chr19:18076210-18076211	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs12980434	chr19:18076221-18076222	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs566296160	chr19:18076246-18076247	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs573983898	chr19:18076313-18076314	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs369237718	chr19:18076337-18076338	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs552951825	chr19:18076358-18076359	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs377072445	chr19:18076369-18076370	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs371691597	chr19:18076397-18076398	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs372560157	chr19:18076402-18076403	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs542900607	chr19:18076446-18076447	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs573088729	chr19:18076457-18076458	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs535615046	chr19:18076458-18076459	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs34297395	chr19:18076459-18076460	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs116405496	chr19:18076483-18076484	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs575443683	chr19:18076544-18076545	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs543960139	chr19:18076545-18076546	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs79682422	chr19:18076546-18076547	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs200444360	chr19:18076547-18076548	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs145040217	chr19:18076567-18076568	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs376263584	chr19:18076611-18076612	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs577517668	chr19:18076619-18076620	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs188891848	chr19:18076632-18076633	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs560388195	chr19:18076649-18076650	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs529524504	chr19:18076653-18076654	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs549201762	chr19:18076663-18076664	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs79257304	chr19:18076692-18076693	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs531881590	chr19:18076713-18076714	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs551539380	chr19:18076723-18076724	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs571625852	chr19:18076726-18076727	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs12981733	chr19:18076768-18076769	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:69)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian cancer	17875760	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:2174 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18065000-18077200	Weak transcription	Fetal Brain Female	brain
2	chr19:18069600-18077600	Weak transcription	Right Atrium	heart
3	chr19:18073400-18076200	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr19:18073400-18076400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr19:18073400-18076600	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr19:18073400-18076600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr19:18073400-18077400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr19:18073600-18076200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr19:18073600-18076800	Weak transcription	K562	blood
10	chr19:18075200-18077600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr19:18075400-18077000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr19:18075600-18076200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr19:18076000-18076400	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr19:18076000-18077600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr19:18076200-18076600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr19:18076200-18077000	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr19:18076200-18077400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr19:18076200-18077600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr19:18076400-18077200	Bivalent Enhancer	HepG2	liver
20	chr19:18076400-18077600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr19:18076400-18077600	Bivalent Enhancer	Fetal Intestine Large	intestine
22	chr19:18076400-18077600	Bivalent Enhancer	Fetal Intestine Small	intestine
23	chr19:18076600-18077000	Enhancers	H1 Cell Line	embryonic stem cell
24	chr19:18076600-18077200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr19:18076600-18077200	Enhancers	A549	lung
26	chr19:18076600-18077400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
27	chr19:18076600-18077600	Bivalent Enhancer	Fetal Muscle Leg	muscle
28	chr19:18076800-18077400	Enhancers	K562	blood
29	chr19:18076800-18077600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
30	chr19:18076800-18077600	Bivalent Enhancer	HUVEC	blood vessel
31	chr19:18077000-18077400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
32	chr19:18077000-18077400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr19:18077000-18077400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr19:18077000-18077400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
35	chr19:18077000-18077400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
36	chr19:18077000-18077400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
37	chr19:18077000-18077400	Bivalent Enhancer	Brain Hippocampus Middle	brain
38	chr19:18077200-18077400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr19:18077200-18077400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr19:18077200-18077400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
41	chr19:18077200-18077400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
42	chr19:18077200-18077400	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr19:18077200-18077400	Bivalent Enhancer	Left Ventricle	heart
44	chr19:18077200-18077800	Flanking Active TSS	Fetal Brain Female	brain
45	chr19:18077200-18078000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr19:18077200-18078000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr19:18077200-18078200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
48	chr19:18077200-18078400	Bivalent Enhancer	Spleen	Spleen
49	chr19:18077200-18078800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
50	chr19:18077200-18079600	Enhancers	Fetal Brain Male	brain

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