Variant report

Variant	esv3355014
Chromosome Location	chr15:40572360-40576658
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:485)
CpG islands
(count:793)
Chromatin interactive
region (count:14)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:485 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr15:40572585-40573004	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr15:40575867-40575959	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr15:40574230-40575035	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr15:40574294-40574494	K562	blood:	n/a	n/a
5	BHLHE40	chr15:40574722-40575324	K562	blood:	n/a	chr15:40574909-40574925
6	BRCA1	chr15:40574445-40574470	HepG2	liver:	n/a	n/a
7	BRCA1	chr15:40573100-40573161	H1-hESC	embryonic stem cell:	n/a	n/a
8	CBX3	chr15:40574263-40574555	K562	blood:	n/a	n/a
9	CBX3	chr15:40574619-40574915	K562	blood:	n/a	n/a
10	CCNT2	chr15:40574052-40575401	K562	blood:	n/a	n/a
11	CHD2	chr15:40574506-40574509	K562	blood:	n/a	n/a
12	CHD2	chr15:40574848-40575010	K562	blood:	n/a	n/a
13	CHD2	chr15:40572815-40572919	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr15:40574357-40574505	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTBP2	chr15:40572719-40576563	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr15:40574360-40574510	GM12873	blood:	n/a	n/a
17	CTCF	chr15:40574540-40574690	HCM	heart:	n/a	n/a
18	CTCF	chr15:40574780-40574930	GM12866	blood:	n/a	chr15:40574821-40574837
19	CTCF	chr15:40574720-40574870	GM12864	blood:	n/a	chr15:40574821-40574837
20	CTCF	chr15:40574700-40574850	AoAF	blood vessel:	n/a	chr15:40574821-40574837
21	CTCF	chr15:40574780-40574930	SAEC	small airway:	n/a	chr15:40574821-40574837
22	CTCF	chr15:40574353-40574464	HepG2	liver:	n/a	n/a
23	CTCF	chr15:40574800-40574950	GM12866	blood:	n/a	chr15:40574821-40574837
24	CTCF	chr15:40574740-40574890	NHEK	skin:	n/a	chr15:40574821-40574837
25	CTCF	chr15:40574760-40574910	BJ	skin:	n/a	chr15:40574821-40574837
26	CTCF	chr15:40574716-40574911	HUVEC	blood vessel:	n/a	chr15:40574821-40574837
27	CTCF	chr15:40575224-40575298	GM19238	blood:	n/a	n/a
28	CTCF	chr15:40574700-40574850	Caco-2	colon:	n/a	chr15:40574821-40574837
29	CTCF	chr15:40574665-40574993	IMR90	lung:	n/a	chr15:40574821-40574837
30	CTCF	chr15:40574260-40574410	GM12872	blood:	n/a	n/a
31	CTCF	chr15:40574720-40574870	SK-N-SH_RA	brain:	n/a	chr15:40574821-40574837
32	CTCF	chr15:40574700-40574850	GM12872	blood:	n/a	chr15:40574821-40574837
33	CTCF	chr15:40574683-40574952	MCF-7	breast:	n/a	chr15:40574821-40574837
34	CTCF	chr15:40574340-40574490	AG09319	gingival:	n/a	n/a
35	CTCF	chr15:40574800-40574950	WI-38	lung:	n/a	chr15:40574821-40574837
36	CTCF	chr15:40574546-40574596	GM13976	blood:	n/a	n/a
37	CTCF	chr15:40574400-40574550	GM12866	blood:	n/a	n/a
38	CTCF	chr15:40574520-40574670	HMEC	breast:	n/a	n/a
39	CTCF	chr15:40574319-40574957	GM19239	blood:	n/a	chr15:40574821-40574837
40	CTCF	chr15:40574596-40575113	MCF-7	breast:	n/a	chr15:40574821-40574837
41	CTCF	chr15:40574760-40574910	NHLF	lung:	n/a	chr15:40574821-40574837
42	CTCF	chr15:40574636-40574957	K562	blood:	n/a	chr15:40574821-40574837
43	CTCF	chr15:40574720-40574870	HA-sp	spinal cord:	n/a	chr15:40574821-40574837
44	CTCF	chr15:40574274-40575061	K562	blood:	n/a	chr15:40574821-40574837
45	CTCF	chr15:40574408-40574434	GM12878	blood:	n/a	n/a
46	CTCF	chr15:40574680-40574830	GM12872	blood:	n/a	n/a
47	CTCF	chr15:40574740-40574890	HMEC	breast:	n/a	chr15:40574821-40574837
48	CTCF	chr15:40575165-40575286	NHEK	skin:	n/a	n/a
49	CTCF	chr15:40574360-40574510	GM06990	blood:	n/a	n/a
50	CTCF	chr15:40574780-40574930	HEK293	kidney:	n/a	chr15:40574821-40574837

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:40575645-40575695	RPTEC	kidney:	n/a
2	chr15:40573976-40574026	SKMC	muscle:	n/a
3	chr15:40575431-40575481	HCF	heart:	n/a
4	chr15:40576538-40576588	MCF-7	breast:	n/a
5	chr15:40573976-40574026	HCF	heart:	n/a
6	chr15:40575645-40575695	GM06990	blood:	n/a
7	chr15:40572794-40572844	HEEpiC	esophagus:	n/a
8	chr15:40573976-40574026	LNCaP	prostate:	n/a
9	chr15:40572550-40572600	AG04450	lung:	fetal
10	chr15:40575431-40575481	H1-hESC	embryonic stem cell:	embryo
11	chr15:40572326-40572376	IMR90	lung:	fetal
12	chr15:40573976-40574026	HRE	kidney:	n/a
13	chr15:40574925-40574975	HCF	heart:	n/a
14	chr15:40576538-40576588	H1-hESC	embryonic stem cell:	embryo
15	chr15:40572326-40572376	SK-N-SH_RA	brain:	n/a
16	chr15:40576538-40576588	SAEC	small airway:	n/a
17	chr15:40575645-40575695	T-47D	breast:	n/a
18	chr15:40573419-40573469	HAEpiC	amniotic membrane:	n/a
19	chr15:40572550-40572600	SKMC	muscle:	n/a
20	chr15:40574925-40574975	ovcar-3	ovarian:	n/a
21	chr15:40575645-40575695	MCF-7	breast:	n/a
22	chr15:40575431-40575481	HEK293	kidney:	embryo
23	chr15:40574697-40574747	MCF-7	breast:	n/a
24	chr15:40574697-40574747	HRE	kidney:	n/a
25	chr15:40575645-40575695	SAEC	small airway:	n/a
26	chr15:40576538-40576588	HRPEpiC	eye:	n/a
27	chr15:40574544-40574594	HNPCEpiC	eye:	n/a
28	chr15:40574544-40574594	HRE	kidney:	n/a
29	chr15:40572550-40572600	HCT-116	colon:	n/a
30	chr15:40576538-40576588	SK-N-SH	brain:	n/a
31	chr15:40572550-40572600	HCPEpiC	choroid plexus:	n/a
32	chr15:40575730-40575780	ECC-1	luminal epithelium:	n/a
33	chr15:40575645-40575695	ProgFib	skin:	n/a
34	chr15:40575356-40575406	LNCaP	prostate:	n/a
35	chr15:40574544-40574594	HCF	heart:	n/a
36	chr15:40574925-40574975	RPTEC	kidney:	n/a
37	chr15:40574697-40574747	BE2_C	brain:	n/a
38	chr15:40574697-40574747	IMR90	lung:	fetal
39	chr15:40574925-40574975	MCF10A-Er-Src	breast:	n/a
40	chr15:40573419-40573469	AoSMC	blood vessel:	n/a
41	chr15:40572550-40572600	HEK293	kidney:	embryo
42	chr15:40574544-40574594	PANC-1	pancreas:	n/a
43	chr15:40575431-40575481	Hela-S3	cervix:	n/a
44	chr15:40575645-40575695	PrEC	prostate:	n/a
45	chr15:40575356-40575406	HIPEpiC	eye:	n/a
46	chr15:40575730-40575780	HNPCEpiC	eye:	n/a
47	chr15:40574544-40574594	HEEpiC	esophagus:	n/a
48	chr15:40573976-40574026	GM12878	blood:	n/a
49	chr15:40574544-40574594	GM12892	blood:	n/a
50	chr15:40572326-40572376	NHDF-neo	bronchial:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:40572270..40573835-chr15:40597340..40599224,2	MCF-7	breast:
2	chr15:40569115..40573106-chr15:40573581..40578796,5	K562	blood:
3	chr15:40573168..40574775-chr15:40591087..40593590,2	K562	blood:
4	chr15:40571973..40573796-chr15:40712353..40713860,2	K562	blood:
5	chr15:40571544..40572394-chr15:40629960..40630610,3	K562	blood:
6	chr15:40574062..40576054-chr15:40576149..40578391,2	K562	blood:
7	chr15:40571284..40573045-chr15:40595754..40597845,2	K562	blood:
8	chr15:40571385..40572541-chr15:40629850..40630639,3	MCF-7	breast:
9	chr15:40575404..40577527-chr15:40578874..40580653,2	MCF-7	breast:
10	chr15:40575377..40577430-chr15:40595263..40597103,2	K562	blood:
11	chr15:40573917..40574516-chr15:40601900..40602438,2	MCF-7	breast:
12	chr15:40566616..40567536-chr15:40575443..40576329,2	K562	blood:
13	chr15:40572393..40574286-chr15:40615089..40617839,2	K562	blood:
14	chr15:40574554..40576537-chr15:40576629..40578391,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLCB2-1	chr15:40576640-40576732	NONHSAT041820

No data

Variant related genes	Relation type
ANKRD63	TF binding region
ANKRD63	CpG island
ENSG00000259307	chromatin interactions
ENSG00000137841	chromatin interactions
ENSG00000230778	chromatin interactions
ENSG00000188549	chromatin interactions
ENSG00000259330	chromatin interactions

Extended variants
information (count: 155 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:155 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372140271	chr15:40572401-40572402	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs569277783	chr15:40572406-40572407	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs560241460	chr15:40572459-40572460	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs373460836	chr15:40572474-40572475	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs548895548	chr15:40572504-40572505	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs568427928	chr15:40572543-40572544	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs534096998	chr15:40572551-40572552	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs573733282	chr15:40572575-40572576	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs553988480	chr15:40572611-40572612	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs376212622	chr15:40572621-40572622	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs142549856	chr15:40572627-40572628	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs150992135	chr15:40572657-40572658	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs527773409	chr15:40572700-40572701	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs538765293	chr15:40572716-40572717	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs558263582	chr15:40572718-40572719	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs575222635	chr15:40572733-40572734	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs139912528	chr15:40572793-40572794	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs201967043	chr15:40572815-40572816	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs554870342	chr15:40572820-40572821	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs143530684	chr15:40572833-40572834	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs370604572	chr15:40572872-40572873	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs10851394	chr15:40572882-40572883	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs112643887	chr15:40572883-40572884	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs113054975	chr15:40572884-40572885	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs546328262	chr15:40572920-40572921	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs562721625	chr15:40572931-40572932	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs78661670	chr15:40572941-40572942	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs140372437	chr15:40572964-40572965	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs568365055	chr15:40572994-40572995	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs527986035	chr15:40573030-40573031	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs547573874	chr15:40573074-40573075	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs565472784	chr15:40573105-40573106	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs370539629	chr15:40573106-40573107	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs11633123	chr15:40573114-40573115	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs538333231	chr15:40573144-40573145	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs558653655	chr15:40573148-40573149	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs568875741	chr15:40573156-40573157	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs55927878	chr15:40573201-40573202	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs554609987	chr15:40573208-40573209	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs181004197	chr15:40573215-40573216	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs76247836	chr15:40573250-40573251	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs150196864	chr15:40573275-40573276	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs75342191	chr15:40573278-40573279	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs545968350	chr15:40573317-40573318	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs562956848	chr15:40573329-40573330	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs531736487	chr15:40573372-40573373	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs183696897	chr15:40573376-40573377	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs561782191	chr15:40573381-40573382	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs112189073	chr15:40573398-40573399	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs547732005	chr15:40573401-40573402	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21129771	CNVD
Breast cancer	21045282	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:40568000-40573400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:40569000-40573800	Weak transcription	Pancreas	Pancrea
3	chr15:40569400-40572800	Bivalent Enhancer	Fetal Muscle Leg	muscle
4	chr15:40570400-40572400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
5	chr15:40571000-40572600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr15:40571000-40572800	Bivalent Enhancer	Fetal Lung	lung
7	chr15:40571000-40574600	Enhancers	Fetal Heart	heart
8	chr15:40571400-40572600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
9	chr15:40571600-40572600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
10	chr15:40571600-40572800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
11	chr15:40571600-40573000	Bivalent Enhancer	Stomach Mucosa	stomach
12	chr15:40571600-40574000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
13	chr15:40571600-40576800	Bivalent Enhancer	Fetal Brain Male	brain
14	chr15:40571800-40572400	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
15	chr15:40571800-40572400	Enhancers	Right Ventricle	heart
16	chr15:40571800-40572600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
17	chr15:40571800-40572600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
18	chr15:40571800-40572600	Bivalent/Poised TSS	Fetal Brain Female	brain
19	chr15:40571800-40572800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
20	chr15:40571800-40572800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
21	chr15:40571800-40572800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr15:40571800-40572800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr15:40571800-40572800	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
24	chr15:40571800-40573000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
25	chr15:40571800-40573400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr15:40572000-40572400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr15:40572000-40572400	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr15:40572000-40572400	Bivalent Enhancer	Adipose Nuclei	Adipose
29	chr15:40572000-40572400	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
30	chr15:40572000-40572400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
31	chr15:40572000-40572600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
32	chr15:40572000-40572600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
33	chr15:40572000-40572800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
34	chr15:40572000-40572800	Bivalent Enhancer	Fetal Intestine Small	intestine
35	chr15:40572000-40573600	Bivalent/Poised TSS	Brain Anterior Caudate	brain
36	chr15:40572000-40573600	Weak transcription	Gastric	stomach
37	chr15:40572000-40574000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
38	chr15:40572000-40574000	Bivalent Enhancer	Fetal Intestine Large	intestine
39	chr15:40572000-40574000	Bivalent Enhancer	Fetal Stomach	stomach
40	chr15:40572000-40574400	Weak transcription	Hela-S3	cervix
41	chr15:40572000-40574400	Weak transcription	K562	blood
42	chr15:40572000-40592800	Weak transcription	Dnd41	blood
43	chr15:40572200-40572400	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr15:40572200-40572400	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr15:40572200-40572400	Bivalent Enhancer	Colonic Mucosa	Colon
46	chr15:40572200-40572400	Flanking Bivalent TSS/Enh	HepG2	liver
47	chr15:40572200-40572800	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
48	chr15:40572200-40574000	Weak transcription	Right Atrium	heart
49	chr15:40572400-40572600	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr15:40572400-40572600	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain

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