Variant report

Variant	nsv579633
Chromosome Location	chr19:42925636-42929254
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:379)
CpG islands
(count:489)
Chromatin interactive
region (count:6)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:379 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:42927405-42927427	HepG2	liver:	n/a	n/a
2	ATF2	chr19:42927036-42927474	GM12878	blood:	n/a	n/a
3	BACH1	chr19:42927187-42927770	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr19:42926950-42927301	GM12878	blood:	n/a	n/a
5	BCL3	chr19:42926895-42928320	A549	lung:	n/a	chr19:42927843-42927856 chr19:42927842-42927851 chr19:42927888-42927897 chr19:42927855-42927864
6	BHLHE40	chr19:42927250-42927653	HepG2	liver:	n/a	n/a
7	BHLHE40	chr19:42927069-42928123	GM12878	blood:	n/a	n/a
8	BRCA1	chr19:42927162-42927582	GM12878	blood:	n/a	n/a
9	BRCA1	chr19:42927281-42927600	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr19:42927869-42928021	GM12878	blood:	n/a	n/a
11	CEBPB	chr19:42927467-42928125	A549	lung:	n/a	n/a
12	CEBPB	chr19:42927627-42927885	HepG2	liver:	n/a	n/a
13	CEBPB	chr19:42927592-42927979	A549	lung:	n/a	n/a
14	CEBPB	chr19:42927405-42927967	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr19:42928170-42928496	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr19:42925771-42926067	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr19:42927596-42927980	IMR90	lung:	n/a	n/a
18	CHD1	chr19:42926733-42928070	GM12878	blood:	n/a	n/a
19	CHD1	chr19:42928304-42928485	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD1	chr19:42927123-42927699	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr19:42927905-42928084	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD1	chr19:42926653-42928296	IMR90	lung:	n/a	n/a
23	CHD2	chr19:42927511-42928641	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr19:42927396-42928056	GM12878	blood:	n/a	n/a
25	CREB1	chr19:42927454-42928227	A549	lung:	n/a	n/a
26	CTCF	chr19:42927880-42928030	HCPEpiC	choroid plexus:	n/a	chr19:42927891-42927904
27	CTCF	chr19:42927000-42927150	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr19:42927060-42927210	GM12874	blood:	n/a	n/a
29	CTCF	chr19:42928951-42929104	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr19:42927020-42927170	GM12872	blood:	n/a	n/a
31	CTCF	chr19:42928900-42929050	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr19:42928866-42929148	A549	lung:	n/a	n/a
33	CTCF	chr19:42928980-42929130	HA-sp	spinal cord:	n/a	n/a
34	CTCF	chr19:42928940-42929090	HPF	lung:	n/a	n/a
35	CTCF	chr19:42927940-42928090	GM06990	blood:	n/a	n/a
36	CTCF	chr19:42928802-42929121	K562	blood:	n/a	n/a
37	CTCF	chr19:42928860-42929010	AG04449	skin:	n/a	n/a
38	CTCF	chr19:42928860-42929010	Caco-2	colon:	n/a	n/a
39	CTCF	chr19:42927080-42927230	SAEC	small airway:	n/a	n/a
40	CTCF	chr19:42927080-42927230	GM12873	blood:	n/a	n/a
41	CTCF	chr19:42928906-42929113	HepG2	liver:	n/a	n/a
42	CTCF	chr19:42928812-42928841	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr19:42927240-42927390	GM12874	blood:	n/a	n/a
44	CTCF	chr19:42927140-42927290	GM12864	blood:	n/a	chr19:42927239-42927248
45	CTCF	chr19:42928760-42929321	K562	blood:	n/a	n/a
46	CTCF	chr19:42928943-42929073	Medullo	brain:	n/a	n/a
47	CTCF	chr19:42927980-42928130	HVMF	connective:	n/a	n/a
48	CTCF	chr19:42927020-42927170	GM12865	blood:	n/a	n/a
49	CTCF	chr19:42928920-42929070	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr19:42927788-42928015	Spleen_OC	spleen:	n/a	chr19:42927891-42927904

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:42927668-42927718	HCT-116	colon:	n/a
2	chr19:42927668-42927718	HCT-116	colon:	n/a
3	chr19:42929067-42929117	AG10803	skin:	n/a
4	chr19:42928195-42928245	SAEC	small airway:	n/a
5	chr19:42927286-42927336	K562	blood:	n/a
6	chr19:42927286-42927336	GM19239	blood:	n/a
7	chr19:42929067-42929117	NHDF-neo	bronchial:	n/a
8	chr19:42928015-42928065	HCT-116	colon:	n/a
9	chr19:42927074-42927124	SAEC	small airway:	n/a
10	chr19:42928015-42928065	SK-N-MC	brain:	n/a
11	chr19:42927668-42927718	MCF-7	breast:	n/a
12	chr19:42927676-42927726	RPTEC	kidney:	n/a
13	chr19:42927286-42927336	MCF-7	breast:	n/a
14	chr19:42927668-42927718	GM12878	blood:	n/a
15	chr19:42927668-42927718	U87	brain:	n/a
16	chr19:42927286-42927336	H1-hESC	embryonic stem cell:	embryo
17	chr19:42927668-42927718	AG09319	gingival:	n/a
18	chr19:42927286-42927336	HCT-116	colon:	n/a
19	chr19:42929067-42929117	NB4	blood:	n/a
20	chr19:42929067-42929117	H1-hESC	embryonic stem cell:	embryo
21	chr19:42927676-42927726	ECC-1	luminal epithelium:	n/a
22	chr19:42928597-42928647	BE2_C	brain:	n/a
23	chr19:42927668-42927718	ProgFib	skin:	n/a
24	chr19:42927668-42927718	PANC-1	pancreas:	n/a
25	chr19:42927668-42927718	Jurkat	blood:	n/a
26	chr19:42928597-42928647	HRE	kidney:	n/a
27	chr19:42927286-42927336	AG09309	skin:	n/a
28	chr19:42927074-42927124	Jurkat	blood:	n/a
29	chr19:42927074-42927124	Caco-2	colon:	n/a
30	chr19:42927286-42927336	PrEC	prostate:	n/a
31	chr19:42927676-42927726	HNPCEpiC	eye:	n/a
32	chr19:42928015-42928065	GM12892	blood:	n/a
33	chr19:42928597-42928647	AoSMC	blood vessel:	n/a
34	chr19:42929067-42929117	HepG2	liver:	n/a
35	chr19:42927286-42927336	NT2-D1	testis:	n/a
36	chr19:42927668-42927718	NHDF-neo	bronchial:	n/a
37	chr19:42927676-42927726	HEK293	kidney:	embryo
38	chr19:42929067-42929117	AG04449	skin:	fetal
39	chr19:42927668-42927718	HNPCEpiC	eye:	n/a
40	chr19:42928597-42928647	HMEC	breast:	n/a
41	chr19:42928015-42928065	HIPEpiC	eye:	n/a
42	chr19:42927668-42927718	GM12892	blood:	n/a
43	chr19:42928195-42928245	HCM	heart:	n/a
44	chr19:42927074-42927124	SK-N-MC	brain:	n/a
45	chr19:42927668-42927718	LNCaP	prostate:	n/a
46	chr19:42928195-42928245	HEEpiC	esophagus:	n/a
47	chr19:42928597-42928647	HIPEpiC	eye:	n/a
48	chr19:42927286-42927336	HUVEC	blood vessel:	n/a
49	chr19:42929067-42929117	GM19239	blood:	n/a
50	chr19:42928597-42928647	HRCEpiC	kidney:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:42903448..42905839-chr19:42923535..42926055,2	MCF-7	breast:
2	chr19:42925339..42926995-chr19:42928878..42931861,2	K562	blood:
3	chr19:42927142..42929606-chr19:42930289..42932952,2	MCF-7	breast:
4	chr19:42787574..42789864-chr19:42923760..42926145,2	MCF-7	breast:
5	chr19:42637501..42639898-chr19:42924232..42925782,2	K562	blood:
6	chr19:42924851..42926943-chr19:42928310..42931390,3	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC011497.1-2	chr19:42927907-42929356	ENSG00000213904.4
2	lnc-CXCL17-1	chr19:42928536-42928688	ENSG00000268605.1
3	lnc-AC011497.1-2	chr19:42928421-42929356	ENSG00000213904.4
4	lnc-CXCL17-1	chr19:42928816-42929223	ENSG00000268605.1
5	lnc-AC011497.1-2	chr19:42928465-42929294	ENSG00000213904.4
6	lnc-AC011497.1-2	chr19:42927907-42929356	NONHSAT066551

No data

Variant related genes	Relation type
LIPE	TF binding region
LIPE-AS1	TF binding region
ENSG00000268605	TF binding region
LIPE	CpG island
LIPE-AS1	CpG island
ENSG00000268605	CpG island
ENSG00000213904	chromatin interactions
ENSG00000266226	chromatin interactions
ENSG00000079432	chromatin interactions
ENSG00000268605	chromatin interactions
ENSG00000254887	chromatin interactions
ENSG00000079435	chromatin interactions

Extended variants
information (count: 140 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:140 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34153633	chr19:42925636-42925637	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs538511736	chr19:42925722-42925723	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs561980953	chr19:42925735-42925736	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs191561994	chr19:42925760-42925761	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs183372477	chr19:42925768-42925769	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs148471097	chr19:42925778-42925779	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs536376898	chr19:42925784-42925785	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs186280684	chr19:42925789-42925790	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs570495629	chr19:42925790-42925791	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs538517053	chr19:42925816-42925817	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs139573029	chr19:42925848-42925849	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs149284921	chr19:42925875-42925876	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs190094935	chr19:42925963-42925964	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs578198049	chr19:42926019-42926020	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs182362002	chr19:42926025-42926026	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs568526226	chr19:42926026-42926027	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs186641677	chr19:42926029-42926030	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs527851468	chr19:42926101-42926102	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs549093557	chr19:42926111-42926112	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs35467032	chr19:42926136-42926137	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs144505985	chr19:42926173-42926174	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs531656147	chr19:42926231-42926232	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs148419890	chr19:42926324-42926325	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs144032842	chr19:42926360-42926361	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs538942254	chr19:42926362-42926363	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs547689158	chr19:42926364-42926365	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs565912703	chr19:42926365-42926366	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs35057744	chr19:42926406-42926407	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs35684151	chr19:42926467-42926468	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs572202091	chr19:42926473-42926474	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs35349390	chr19:42926496-42926497	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs146431304	chr19:42926507-42926508	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs558530804	chr19:42926513-42926514	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs576728733	chr19:42926529-42926530	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs545705834	chr19:42926543-42926544	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs554022390	chr19:42926567-42926568	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs572345555	chr19:42926608-42926609	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs542811020	chr19:42926612-42926613	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs561100347	chr19:42926640-42926641	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs139811183	chr19:42926659-42926660	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs543519038	chr19:42926672-42926673	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs565305354	chr19:42926709-42926710	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs532382409	chr19:42926717-42926718	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs547751848	chr19:42926736-42926737	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs565968121	chr19:42926768-42926769	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs192674040	chr19:42926776-42926777	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs548405636	chr19:42926867-42926868	Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs550705830	chr19:42926919-42926920	Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs569709250	chr19:42926934-42926935	Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs144518176	chr19:42926956-42926957	Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
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
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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	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
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Multiple myeloma	17550852	CNVD

Chromatin state (count:600 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42906200-42926200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr19:42906400-42926400	Weak transcription	Colonic Mucosa	Colon
3	chr19:42906600-42926400	Weak transcription	Fetal Lung	lung
4	chr19:42907400-42926600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr19:42909000-42925800	Weak transcription	Dnd41	blood
6	chr19:42912800-42926200	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr19:42913800-42925800	Weak transcription	NHDF-Ad	bronchial
8	chr19:42914000-42926400	Weak transcription	Ovary	ovary
9	chr19:42914400-42926000	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr19:42915200-42925800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr19:42917000-42926200	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr19:42917400-42926600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr19:42919000-42925800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr19:42922800-42926000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr19:42923000-42926200	Enhancers	Left Ventricle	heart
16	chr19:42923000-42926600	Enhancers	Spleen	Spleen
17	chr19:42923200-42926400	Enhancers	Esophagus	oesophagus
18	chr19:42923400-42926200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr19:42923400-42926400	Enhancers	Right Ventricle	heart
20	chr19:42923400-42926800	Enhancers	Fetal Muscle Leg	muscle
21	chr19:42923600-42925800	Flanking Active TSS	Adipose Nuclei	Adipose
22	chr19:42923600-42925800	Enhancers	Brain Hippocampus Middle	brain
23	chr19:42923600-42926200	Enhancers	Brain Cingulate Gyrus	brain
24	chr19:42923600-42926200	Enhancers	Right Atrium	heart
25	chr19:42923600-42926400	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr19:42923600-42926600	Enhancers	HMEC	breast
27	chr19:42923600-42926800	Enhancers	Placenta	Placenta
28	chr19:42924000-42926200	Enhancers	Brain Germinal Matrix	brain
29	chr19:42924000-42926400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
30	chr19:42924000-42926600	Enhancers	Primary T cells from cord blood	blood
31	chr19:42924000-42926600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chr19:42924000-42927200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr19:42924200-42926000	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr19:42924200-42926000	Genic enhancers	Fetal Stomach	stomach
35	chr19:42924200-42926200	Enhancers	Brain Anterior Caudate	brain
36	chr19:42924200-42926400	Enhancers	Brain Angular Gyrus	brain
37	chr19:42924200-42926600	Enhancers	Primary T cells fromperipheralblood	blood
38	chr19:42924200-42926600	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr19:42924200-42926800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr19:42924200-42926800	Enhancers	Lung	lung
41	chr19:42924200-42927000	Enhancers	Pancreas	Pancrea
42	chr19:42924400-42925800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr19:42924400-42925800	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr19:42924400-42925800	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr19:42924400-42926200	Enhancers	Fetal Heart	heart
46	chr19:42924400-42926200	Enhancers	Rectal Mucosa Donor 29	rectum
47	chr19:42924400-42926400	Enhancers	Primary T killer memory cells from peripheral blood	blood
48	chr19:42924400-42926400	Enhancers	Duodenum Mucosa	Duodenum
49	chr19:42924400-42926600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
50	chr19:42924400-42926600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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