Variant report

Variant	esv3405182
Chromosome Location	chr19:38719137-38721685
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr19:38720409-38721016	A549	lung:	n/a	n/a
2	BACH1	chr19:38720556-38720699	K562	blood:	n/a	n/a
3	BCL3	chr19:38720360-38720920	A549	lung:	n/a	n/a
4	BHLHE40	chr19:38720569-38720591	K562	blood:	n/a	n/a
5	CBX3	chr19:38720339-38720680	K562	blood:	n/a	n/a
6	CCNT2	chr19:38720244-38720627	K562	blood:	n/a	chr19:38720534-38720543
7	CHD1	chr19:38719662-38719882	H1-hESC	embryonic stem cell:	n/a	chr19:38719767-38719774
8	CHD2	chr19:38718807-38719471	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr19:38720404-38720762	K562	blood:	n/a	n/a
10	CHD2	chr19:38720378-38720699	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr19:38719171-38719193	HepG2	liver:	n/a	n/a
12	CHD2	chr19:38720364-38720729	Hela-S3	cervix:	n/a	n/a
13	CREB1	chr19:38719389-38719778	A549	lung:	n/a	n/a
14	CREB1	chr19:38720139-38720732	A549	lung:	n/a	n/a
15	CREB1	chr19:38720221-38720604	A549	lung:	n/a	n/a
16	CTBP2	chr19:38720348-38720737	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTBP2	chr19:38719154-38720005	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr19:38720400-38720550	GM12867	blood:	n/a	chr19:38720402-38720415 chr19:38720482-38720492
19	CTCF	chr19:38720474-38720483	GM19240	blood:	n/a	n/a
20	CTCF	chr19:38721460-38721610	A549	lung:	n/a	n/a
21	CTCF	chr19:38720480-38720630	Caco-2	colon:	n/a	chr19:38720482-38720492
22	CTCF	chr19:38720340-38720490	HEK293	kidney:	n/a	chr19:38720402-38720415
23	CTCF	chr19:38720400-38720550	GM12866	blood:	n/a	chr19:38720402-38720415 chr19:38720482-38720492
24	CTCF	chr19:38720380-38720530	GM12870	blood:	n/a	chr19:38720402-38720415 chr19:38720482-38720492
25	CTCF	chr19:38720360-38720510	BJ	skin:	n/a	chr19:38720402-38720415 chr19:38720482-38720492
26	CTCF	chr19:38720292-38720543	K562	blood:	n/a	chr19:38720402-38720415 chr19:38720482-38720492
27	CTCF	chr19:38720431-38720439	GM19240	blood:	n/a	n/a
28	CTCF	chr19:38720400-38720550	HMF	breast:	n/a	chr19:38720402-38720415 chr19:38720482-38720492
29	CTCF	chr19:38719520-38719670	BJ	skin:	n/a	chr19:38719523-38719541
30	CTCF	chr19:38720500-38720650	NHDF-neo	bronchial:	n/a	n/a
31	CTCF	chr19:38720380-38720530	GM12871	blood:	n/a	chr19:38720402-38720415 chr19:38720482-38720492
32	CTCF	chr19:38720452-38720522	GM12891	blood:	n/a	chr19:38720482-38720492
33	CTCF	chr19:38720420-38720570	HCPEpiC	choroid plexus:	n/a	chr19:38720482-38720492
34	CTCF	chr19:38720320-38720470	HCM	heart:	n/a	chr19:38720402-38720415
35	CTCF	chr19:38720500-38720650	A549	lung:	n/a	n/a
36	CTCF	chr19:38720380-38720530	AG04449	skin:	n/a	chr19:38720402-38720415 chr19:38720482-38720492
37	CTCF	chr19:38720400-38720600	K562	blood:	n/a	chr19:38720402-38720415 chr19:38720482-38720492
38	CTCF	chr19:38720420-38720570	HA-sp	spinal cord:	n/a	chr19:38720482-38720492
39	CTCF	chr19:38720360-38720510	SK-N-SH_RA	brain:	n/a	chr19:38720402-38720415 chr19:38720482-38720492
40	CTCF	chr19:38720400-38720550	BJ	skin:	n/a	chr19:38720402-38720415 chr19:38720482-38720492
41	CTCF	chr19:38720387-38720564	GM12878	blood:	n/a	chr19:38720402-38720415 chr19:38720482-38720492
42	CTCF	chr19:38720291-38720578	K562	blood:	n/a	chr19:38720402-38720415 chr19:38720482-38720492
43	CTCF	chr19:38719500-38719650	K562	blood:	n/a	chr19:38719523-38719541
44	CTCF	chr19:38720420-38720570	HUVEC	blood vessel:	n/a	chr19:38720482-38720492
45	CTCF	chr19:38720316-38720595	IMR90	lung:	n/a	chr19:38720402-38720415 chr19:38720482-38720492
46	CTCF	chr19:38719420-38719570	HRE	kidney:	n/a	chr19:38719523-38719541
47	CTCF	chr19:38720320-38720470	HFF	foreskin:	n/a	chr19:38720402-38720415
48	CTCF	chr19:38720400-38720550	AG10803	skin:	n/a	chr19:38720402-38720415 chr19:38720482-38720492
49	CTCF	chr19:38720463-38720470	GM19240	blood:	n/a	n/a
50	CTCF	chr19:38719460-38719610	HUVEC	blood vessel:	n/a	chr19:38719523-38719541

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:38721070-38721120	ovcar-3	ovarian:	n/a
2	chr19:38720072-38720122	HAEpiC	amniotic membrane:	n/a
3	chr19:38720235-38720285	IMR90	lung:	fetal
4	chr19:38720072-38720122	A549	lung:	n/a
5	chr19:38719523-38719573	SK-N-SH_RA	brain:	n/a
6	chr19:38720689-38720739	U87	brain:	n/a
7	chr19:38720626-38720676	BJ	skin:	n/a
8	chr19:38720689-38720739	AG10803	skin:	n/a
9	chr19:38720689-38720739	HRE	kidney:	n/a
10	chr19:38720072-38720122	PANC-1	pancreas:	n/a
11	chr19:38720235-38720285	Caco-2	colon:	n/a
12	chr19:38720235-38720285	HepG2	liver:	n/a
13	chr19:38720072-38720122	HCM	heart:	n/a
14	chr19:38720072-38720122	Jurkat	blood:	n/a
15	chr19:38720072-38720122	HCT-116	colon:	n/a
16	chr19:38720235-38720285	HCPEpiC	choroid plexus:	n/a
17	chr19:38720626-38720676	U87	brain:	n/a
18	chr19:38720072-38720122	HIPEpiC	eye:	n/a
19	chr19:38720072-38720122	HEK293	kidney:	embryo
20	chr19:38720235-38720285	AG04449	skin:	fetal
21	chr19:38721070-38721120	SAEC	small airway:	n/a
22	chr19:38720689-38720739	HRPEpiC	eye:	n/a
23	chr19:38720689-38720739	HL-60	blood:	n/a
24	chr19:38721070-38721120	PrEC	prostate:	n/a
25	chr19:38719523-38719573	HL-60	blood:	n/a
26	chr19:38721070-38721120	NHBE	bronchial:	n/a
27	chr19:38720626-38720676	AG10803	skin:	n/a
28	chr19:38720626-38720676	Hepatocyte	liver:	n/a
29	chr19:38719523-38719573	SAEC	small airway:	n/a
30	chr19:38720235-38720285	A549	lung:	n/a
31	chr19:38720626-38720676	ProgFib	skin:	n/a
32	chr19:38719523-38719573	HCT-116	colon:	n/a
33	chr19:38720689-38720739	BJ	skin:	n/a
34	chr19:38721070-38721120	GM06990	blood:	n/a
35	chr19:38720626-38720676	NT2-D1	testis:	n/a
36	chr19:38720072-38720122	Caco-2	colon:	n/a
37	chr19:38720235-38720285	HRE	kidney:	n/a
38	chr19:38720072-38720122	NH-A	brain:	n/a
39	chr19:38720235-38720285	PFSK-1	brain:	n/a
40	chr19:38720235-38720285	GM12892	blood:	n/a
41	chr19:38720072-38720122	GM19239	blood:	n/a
42	chr19:38719523-38719573	ECC-1	luminal epithelium:	n/a
43	chr19:38720072-38720122	LNCaP	prostate:	n/a
44	chr19:38720235-38720285	BE2_C	brain:	n/a
45	chr19:38721070-38721120	AG09319	gingival:	n/a
46	chr19:38720689-38720739	CMK	blood:	n/a
47	chr19:38720235-38720285	HEK293	kidney:	embryo
48	chr19:38720626-38720676	GM12892	blood:	n/a
49	chr19:38719523-38719573	GM12892	blood:	n/a
50	chr19:38721070-38721120	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:38718989..38720789-chr19:38865301..38866855,2	MCF-7	breast:
2	chr19:38717810..38720228-chr19:38876711..38878921,2	K562	blood:
3	chr19:38711348..38714655-chr19:38718716..38721513,3	MCF-7	breast:
4	chr19:38718052..38720655-chr19:38755234..38758069,2	MCF-7	breast:
5	chr19:38720592..38722293-chr19:38724613..38726835,2	MCF-7	breast:
6	chr19:38715608..38719883-chr19:38825304..38828918,6	K562	blood:
7	chr19:38718266..38721870-chr19:38794040..38798765,4	MCF-7	breast:
8	chr19:38713393..38715847-chr19:38720638..38723523,2	K562	blood:
9	chr19:38720868..38723162-chr19:38725359..38727589,2	K562	blood:
10	chr19:38720388..38721001-chr19:38825841..38826415,2	K562	blood:
11	chr19:38720504..38722100-chr19:38877148..38880133,2	K562	blood:
12	chr19:38719348..38721458-chr19:38874867..38876458,2	K562	blood:
13	chr19:38705043..38707659-chr19:38719005..38721797,2	K562	blood:
14	chr19:38713729..38715404-chr19:38717530..38720413,2	K562	blood:

Variant related genes	Relation type
DPF1	TF binding region
DPF1	CpG island
ENSG00000167644	chromatin interactions
ENSG00000188766	chromatin interactions
ENSG00000099341	chromatin interactions
ENSG00000267090	chromatin interactions
ENSG00000167642	chromatin interactions
ENSG00000099338	chromatin interactions
ENSG00000179168	chromatin interactions
ENSG00000167645	chromatin interactions
ENSG00000011332	chromatin interactions

Extended variants
information (count: 73 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:73 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556565024	chr19:38719148-38719149	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs568496224	chr19:38719158-38719159	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs368058678	chr19:38719241-38719242	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs8101485	chr19:38719302-38719303	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs547812418	chr19:38719332-38719333	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs557564017	chr19:38719366-38719367	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs569037897	chr19:38719398-38719399	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs540428956	chr19:38719404-38719405	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs73630123	chr19:38719409-38719410	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs374330488	chr19:38719497-38719498	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs574358323	chr19:38719696-38719697	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs544906943	chr19:38719718-38719719	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs562912629	chr19:38719736-38719737	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs149495200	chr19:38719784-38719785	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs545523872	chr19:38719807-38719808	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs560344093	chr19:38719854-38719855	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs528304609	chr19:38719865-38719866	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs368722142	chr19:38719930-38719931	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs568225716	chr19:38719958-38719959	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs189676808	chr19:38719964-38719965	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs550450211	chr19:38720048-38720049	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs568559347	chr19:38720098-38720099	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs538997169	chr19:38720104-38720105	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs557841714	chr19:38720426-38720427	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs566409105	chr19:38720479-38720480	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs10412116	chr19:38720538-38720539	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs555719267	chr19:38720555-38720556	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs376359623	chr19:38720579-38720580	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs529846356	chr19:38720623-38720624	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs113536049	chr19:38720633-38720634	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs574276802	chr19:38720723-38720724	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs182747974	chr19:38720734-38720735	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs143944138	chr19:38720756-38720757	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs578077238	chr19:38720777-38720778	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs545041044	chr19:38720812-38720813	Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs560659244	chr19:38720854-38720855	Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs527812332	chr19:38720879-38720880	Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs543091559	chr19:38720909-38720910	Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs187271618	chr19:38720956-38720957	Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs192067682	chr19:38721029-38721030	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs73028390	chr19:38721038-38721039	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs117439274	chr19:38721067-38721068	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs532778206	chr19:38721070-38721071	Weak transcription Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs183509895	chr19:38721105-38721106	Weak transcription Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs564389159	chr19:38721109-38721110	Weak transcription Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs566439000	chr19:38721156-38721157	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs533693762	chr19:38721200-38721201	Weak transcription Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs368981364	chr19:38721234-38721235	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs188396359	chr19:38721238-38721239	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs570002387	chr19:38721269-38721270	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Mental retardation	19951919	CNVD
19q13.11 deletion syndrome	22378287	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD

Chromatin state (count:266 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:38715200-38719200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr19:38715200-38719200	Weak transcription	Pancreas	Pancrea
3	chr19:38715400-38719200	Weak transcription	NH-A	brain
4	chr19:38715400-38719200	Weak transcription	NHDF-Ad	bronchial
5	chr19:38715600-38719400	Weak transcription	Brain Anterior Caudate	brain
6	chr19:38715600-38719600	Weak transcription	Hela-S3	cervix
7	chr19:38716600-38719200	Enhancers	A549	lung
8	chr19:38716600-38720800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
9	chr19:38716800-38719200	Enhancers	Fetal Brain Male	brain
10	chr19:38717400-38719200	Weak transcription	Brain Cingulate Gyrus	brain
11	chr19:38717600-38719400	Weak transcription	K562	blood
12	chr19:38718000-38720800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr19:38718200-38720000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
14	chr19:38718400-38719600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
15	chr19:38718400-38719600	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
16	chr19:38718400-38720600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
17	chr19:38718400-38721000	Active TSS	iPS-15b Cell Line	embryonic stem cell
18	chr19:38718600-38719200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr19:38718600-38719200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr19:38718600-38719200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
21	chr19:38718600-38719200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
22	chr19:38718600-38719200	Bivalent Enhancer	Fetal Muscle Leg	muscle
23	chr19:38718600-38719200	Bivalent Enhancer	Fetal Stomach	stomach
24	chr19:38718600-38719400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
25	chr19:38718600-38719400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr19:38718600-38719400	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
27	chr19:38718600-38719400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
28	chr19:38718600-38719800	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
29	chr19:38718600-38719800	Bivalent Enhancer	Fetal Thymus	thymus
30	chr19:38718600-38720000	Bivalent Enhancer	Primary T cells from cord blood	blood
31	chr19:38718600-38720200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr19:38718600-38720600	Active TSS	Brain Angular Gyrus	brain
33	chr19:38718600-38720600	Active TSS	Right Ventricle	heart
34	chr19:38718600-38720800	Active TSS	H9 Cell Line	embryonic stem cell
35	chr19:38718800-38719200	Active TSS	iPS-18 Cell Line	embryonic stem cell
36	chr19:38718800-38719200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
37	chr19:38718800-38719400	Active TSS	Cortex derived primary cultured neurospheres	brain
38	chr19:38718800-38719800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
39	chr19:38718800-38720000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
40	chr19:38718800-38720200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
41	chr19:38718800-38720600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr19:38718800-38720600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr19:38718800-38720800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
44	chr19:38718800-38720800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
45	chr19:38718800-38720800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
46	chr19:38718800-38721000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr19:38718800-38721000	Active TSS	Brain Inferior Temporal Lobe	brain
48	chr19:38718800-38721200	Active TSS	Brain Germinal Matrix	brain
49	chr19:38718800-38721200	Active TSS	Fetal Brain Female	brain
50	chr19:38719000-38719200	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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