Variant report

Variant	esv3358201
Chromosome Location	chr19:18058077-18060550
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:420)
CpG islands
(count:366)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:420 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr19:18058859-18059221	GM12878	blood:	n/a	n/a
2	ATF3	chr19:18058579-18058890	A549	lung:	n/a	n/a
3	ATF3	chr19:18058576-18058889	A549	lung:	n/a	n/a
4	ATF3	chr19:18058632-18058894	K562	blood:	n/a	n/a
5	BACH1	chr19:18060112-18060197	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr19:18058695-18059233	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr19:18058516-18058907	GM12878	blood:	n/a	chr19:18058846-18058855 chr19:18058697-18058706
8	BCL3	chr19:18058935-18059299	GM12878	blood:	n/a	chr19:18059198-18059207
9	BHLHE40	chr19:18058291-18058883	K562	blood:	n/a	n/a
10	BHLHE40	chr19:18058341-18059262	GM12878	blood:	n/a	chr19:18059182-18059198
11	BRCA1	chr19:18058220-18058336	HepG2	liver:	n/a	n/a
12	CCNT2	chr19:18058631-18059287	K562	blood:	n/a	chr19:18058987-18058996 chr19:18058920-18058929 chr19:18058927-18058936
13	CEBPB	chr19:18058933-18059149	GM12878	blood:	n/a	n/a
14	CEBPD	chr19:18058876-18059128	HepG2	liver:	n/a	n/a
15	CEBPD	chr19:18058616-18058838	HepG2	liver:	n/a	n/a
16	CHD2	chr19:18058760-18058768	HepG2	liver:	n/a	n/a
17	CHD2	chr19:18058316-18059187	H1-hESC	embryonic stem cell:	n/a	chr19:18058988-18058998
18	CHD2	chr19:18058714-18059133	K562	blood:	n/a	chr19:18058988-18058998
19	CHD2	chr19:18059550-18060229	GM12878	blood:	n/a	n/a
20	CHD2	chr19:18060112-18060122	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr19:18058339-18059236	Hela-S3	cervix:	n/a	chr19:18058988-18058998
22	CHD2	chr19:18058368-18059176	GM12878	blood:	n/a	chr19:18058988-18058998
23	CHD2	chr19:18059528-18059809	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr19:18058319-18058919	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr19:18058961-18059256	A549	lung:	n/a	n/a
26	CREB1	chr19:18058494-18058892	A549	lung:	n/a	n/a
27	CREB1	chr19:18058201-18058806	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr19:18058280-18058430	GM12871	blood:	n/a	n/a
29	CTCF	chr19:18058440-18058590	HMF	breast:	n/a	n/a
30	CTCF	chr19:18058400-18058550	HepG2	liver:	n/a	n/a
31	CTCF	chr19:18058360-18058510	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr19:18058340-18058490	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr19:18058280-18058430	RPTEC	kidney:	n/a	n/a
34	CTCF	chr19:18058440-18058590	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr19:18058532-18058562	GM19239	blood:	n/a	n/a
36	CTCF	chr19:18058360-18058510	GM12878	blood:	n/a	n/a
37	CTCF	chr19:18058360-18058510	GM12873	blood:	n/a	n/a
38	CTCF	chr19:18058140-18058290	GM12878	blood:	n/a	n/a
39	CTCF	chr19:18058400-18058550	GM12869	blood:	n/a	n/a
40	CTCF	chr19:18058440-18058590	GM12866	blood:	n/a	n/a
41	CTCF	chr19:18058340-18058490	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr19:18058420-18058570	K562	blood:	n/a	n/a
43	CTCF	chr19:18058340-18058490	GM12864	blood:	n/a	n/a
44	CTCF	chr19:18058460-18058610	GM12868	blood:	n/a	n/a
45	CTCF	chr19:18058400-18058550	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr19:18058260-18058410	HAc	cerebellar:	n/a	n/a
47	CTCF	chr19:18058400-18058550	GM12873	blood:	n/a	n/a
48	CTCF	chr19:18058440-18058590	AG04450	lung:	n/a	n/a
49	CTCF	chr19:18058360-18058510	BJ	skin:	n/a	n/a
50	CTCF	chr19:18058673-18058801	Pancreas_OC	pancreas:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:18060024-18060074	K562	blood:	n/a
2	chr19:18060024-18060074	MCF-7	breast:	n/a
3	chr19:18059878-18059928	HMEC	breast:	n/a
4	chr19:18059054-18059104	NH-A	brain:	n/a
5	chr19:18059054-18059104	AG04450	lung:	fetal
6	chr19:18059054-18059104	HCPEpiC	choroid plexus:	n/a
7	chr19:18060024-18060074	NH-A	brain:	n/a
8	chr19:18060024-18060074	NB4	blood:	n/a
9	chr19:18059042-18059092	PFSK-1	brain:	n/a
10	chr19:18059054-18059104	AoSMC	blood vessel:	n/a
11	chr19:18059054-18059104	SKMC	muscle:	n/a
12	chr19:18059878-18059928	RPTEC	kidney:	n/a
13	chr19:18059054-18059104	NHBE	bronchial:	n/a
14	chr19:18058438-18058488	AG04449	skin:	fetal
15	chr19:18059042-18059092	CMK	blood:	n/a
16	chr19:18058438-18058488	AG09319	gingival:	n/a
17	chr19:18060024-18060074	SKMC	muscle:	n/a
18	chr19:18059042-18059092	NHDF-neo	bronchial:	n/a
19	chr19:18059878-18059928	HCM	heart:	n/a
20	chr19:18058885-18058935	HCPEpiC	choroid plexus:	n/a
21	chr19:18058438-18058488	SK-N-MC	brain:	n/a
22	chr19:18059042-18059092	HRE	kidney:	n/a
23	chr19:18059878-18059928	K562	blood:	n/a
24	chr19:18058438-18058488	Hepatocyte	liver:	n/a
25	chr19:18058438-18058488	NHBE	bronchial:	n/a
26	chr19:18060024-18060074	Hela-S3	cervix:	n/a
27	chr19:18059042-18059092	AG04449	skin:	fetal
28	chr19:18059042-18059092	A549	lung:	n/a
29	chr19:18059054-18059104	GM12892	blood:	n/a
30	chr19:18059042-18059092	GM12891	blood:	n/a
31	chr19:18058438-18058488	AoSMC	blood vessel:	n/a
32	chr19:18059042-18059092	ECC-1	luminal epithelium:	n/a
33	chr19:18058438-18058488	A549	lung:	n/a
34	chr19:18058438-18058488	HCPEpiC	choroid plexus:	n/a
35	chr19:18059878-18059928	AG10803	skin:	n/a
36	chr19:18058438-18058488	HL-60	blood:	n/a
37	chr19:18058885-18058935	BJ	skin:	n/a
38	chr19:18060024-18060074	NHBE	bronchial:	n/a
39	chr19:18059878-18059928	SK-N-SH_RA	brain:	n/a
40	chr19:18059054-18059104	HRCEpiC	kidney:	n/a
41	chr19:18060024-18060074	HAEpiC	amniotic membrane:	n/a
42	chr19:18058438-18058488	NHDF-neo	bronchial:	n/a
43	chr19:18059042-18059092	HRCEpiC	kidney:	n/a
44	chr19:18060024-18060074	U87	brain:	n/a
45	chr19:18058438-18058488	ovcar-3	ovarian:	n/a
46	chr19:18058438-18058488	HMEC	breast:	n/a
47	chr19:18058885-18058935	HPAEpiC	pulmonary alveolar:	n/a
48	chr19:18059878-18059928	SK-N-MC	brain:	n/a
49	chr19:18060024-18060074	T-47D	breast:	n/a
50	chr19:18059878-18059928	AG04450	lung:	fetal

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:18049354..18052020-chr19:18056652..18058961,3	MCF-7	breast:
2	chr19:18058855..18062679-chr19:18075387..18079032,3	MCF-7	breast:
3	chr19:18057965..18060030-chr19:18157844..18159639,2	K562	blood:
4	chr19:18058378..18059062-chr19:18111827..18112579,2	MCF-7	breast:
5	chr19:18058787..18061046-chr19:18077855..18080971,5	K562	blood:
6	chr19:18057229..18058563-chr19:18107268..18108242,5	MCF-7	breast:
7	chr19:18057024..18060346-chr19:18095045..18097691,3	K562	blood:
8	chr19:17969435..17972591-chr19:18056494..18062279,6	K562	blood:
9	chr19:18057341..18060009-chr19:18227603..18230383,4	K562	blood:
10	chr19:18056470..18058244-chr19:18107377..18108277,8	MCF-7	breast:
11	chr19:17984874..17987363-chr19:18056604..18058812,2	K562	blood:
12	chr19:18057399..18062095-chr19:18108081..18112546,5	K562	blood:
13	chr19:18059749..18060616-chr19:18107405..18108095,3	MCF-7	breast:
14	chr19:18057090..18059767-chr19:18110634..18113948,3	MCF-7	breast:
15	chr19:17969156..17972643-chr19:18057294..18060299,6	K562	blood:
16	chr19:18057353..18059947-chr19:18110814..18113485,3	MCF-7	breast:
17	chr19:18058545..18060351-chr19:18094684..18096854,2	MCF-7	breast:
18	chr19:18055988..18065489-chr19:18073307..18083163,16	K562	blood:
19	chr19:18060053..18061688-chr19:18218502..18220719,2	K562	blood:
20	chr19:18058858..18061007-chr19:18390720..18393623,2	K562	blood:
21	chr19:18059452..18062098-chr19:18102180..18104149,2	MCF-7	breast:
22	chr19:17970109..17972099-chr19:18059372..18061707,2	MCF-7	breast:
23	chr19:18058883..18061817-chr19:18083400..18086380,2	K562	blood:
24	chr19:18052069..18059812-chr19:18106129..18113779,16	K562	blood:
25	chr19:18056861..18058558-chr19:18107372..18108294,7	K562	blood:
26	chr19:17974807..17978167-chr19:18058036..18060976,4	K562	blood:

No data

Variant related genes	Relation type
KCNN1	TF binding region
KCNN1	CpG island
ENSG00000243455	chromatin interactions
ENSG00000105642	chromatin interactions
ENSG00000105640	chromatin interactions
ENSG00000252591	chromatin interactions
ENSG00000105643	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000267959	chromatin interactions

Extended variants
information (count: 66 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:66 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548374078	chr19:18058101-18058102	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs562159656	chr19:18058137-18058138	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs191977791	chr19:18058206-18058207	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs12985086	chr19:18058212-18058213	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs73526372	chr19:18058236-18058237	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs538461455	chr19:18058241-18058242	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs551986327	chr19:18058331-18058332	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs565516390	chr19:18058433-18058434	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs76559458	chr19:18058439-18058440	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs141437384	chr19:18058462-18058463	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs574381370	chr19:18058490-18058491	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs34931504	chr19:18058536-18058537	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs538208620	chr19:18058611-18058612	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs557654393	chr19:18058695-18058696	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs577581529	chr19:18058705-18058706	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs200917025	chr19:18058733-18058734	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs4808724	chr19:18058753-18058754	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs4808725	chr19:18058823-18058824	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs573474943	chr19:18058827-18058828	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs542351092	chr19:18058883-18058884	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs111652769	chr19:18058903-18058904	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs534869219	chr19:18058917-18058918	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs184929214	chr19:18059041-18059042	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs530938552	chr19:18059043-18059044	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs550673960	chr19:18059057-18059058	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs376804561	chr19:18059219-18059220	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs62119775	chr19:18059322-18059323	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs532299777	chr19:18059547-18059548	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs75916935	chr19:18059673-18059674	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs552047505	chr19:18059679-18059680	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs144200872	chr19:18059684-18059685	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs565578541	chr19:18059714-18059715	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs12609274	chr19:18059744-18059745	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs116837258	chr19:18059902-18059903	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs557881297	chr19:18059910-18059911	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs568034032	chr19:18059921-18059922	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs138418421	chr19:18059984-18059985	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs556718374	chr19:18059992-18059993	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs76989713	chr19:18060047-18060048	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs143925553	chr19:18060062-18060063	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs553696952	chr19:18060076-18060077	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs189440503	chr19:18060079-18060080	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs181203996	chr19:18060109-18060110	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs542013861	chr19:18060134-18060135	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs555853970	chr19:18060170-18060171	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs370452443	chr19:18060192-18060193	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs544668831	chr19:18060298-18060299	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs556743471	chr19:18060299-18060300	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs564184279	chr19:18060313-18060314	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs533143633	chr19:18060315-18060316	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

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

Chromatin state (count:544 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18044600-18058200	Weak transcription	Psoas Muscle	Psoas
2	chr19:18044800-18058200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr19:18047800-18058200	Weak transcription	Left Ventricle	heart
4	chr19:18051200-18058200	Weak transcription	Aorta	Aorta
5	chr19:18054200-18058200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr19:18054800-18058200	Weak transcription	Fetal Lung	lung
7	chr19:18055000-18058200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr19:18055000-18058200	Weak transcription	Right Ventricle	heart
9	chr19:18055200-18058200	Weak transcription	Ovary	ovary
10	chr19:18055200-18058200	Weak transcription	HSMM	muscle
11	chr19:18055400-18058200	Weak transcription	Gastric	stomach
12	chr19:18055600-18058200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr19:18055600-18058200	Weak transcription	HSMMtube	muscle
14	chr19:18055600-18058200	Weak transcription	NHLF	lung
15	chr19:18055800-18058200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr19:18056000-18058200	Weak transcription	Esophagus	oesophagus
17	chr19:18056800-18058200	Enhancers	Primary B cells from peripheral blood	blood
18	chr19:18057200-18058200	Enhancers	Fetal Thymus	thymus
19	chr19:18057800-18058200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr19:18057800-18058200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr19:18057800-18058200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr19:18057800-18058200	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr19:18057800-18058200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr19:18057800-18058200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr19:18057800-18058200	Enhancers	Placenta	Placenta
26	chr19:18057800-18058400	Enhancers	Spleen	Spleen
27	chr19:18057800-18058400	Flanking Active TSS	GM12878-XiMat	blood
28	chr19:18057800-18058600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
29	chr19:18057800-18058600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr19:18058000-18058200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
31	chr19:18058000-18058200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr19:18058000-18058200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr19:18058000-18058200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr19:18058000-18058200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr19:18058000-18058200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
36	chr19:18058000-18058200	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr19:18058000-18058200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr19:18058000-18058200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
39	chr19:18058000-18058200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr19:18058000-18058200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr19:18058000-18058200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr19:18058000-18058200	Enhancers	Muscle Satellite Cultured Cells	--
43	chr19:18058000-18058200	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr19:18058000-18058200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr19:18058000-18058200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr19:18058000-18058200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr19:18058000-18058200	Enhancers	Liver	Liver
48	chr19:18058000-18058200	Enhancers	Brain Germinal Matrix	brain
49	chr19:18058000-18058200	Enhancers	Duodenum Mucosa	Duodenum
50	chr19:18058000-18058200	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum

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