Variant report

Variant	nsv517068
Chromosome Location	chr15:77254544-77381222
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3008)
CpG islands
(count:2570)
Chromatin interactive
region (count:110)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3008 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:77324454-77324600	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:77359696-77360073	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:77360322-77360620	K562	blood:	n/a	n/a
4	ARID3A	chr15:77356962-77357653	K562	blood:	n/a	n/a
5	ARID3A	chr15:77357124-77357218	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:77359749-77360087	K562	blood:	n/a	n/a
7	ATF1	chr15:77377561-77377886	K562	blood:	n/a	n/a
8	ATF1	chr15:77356868-77357302	K562	blood:	n/a	n/a
9	ATF2	chr15:77314226-77314800	GM12878	blood:	n/a	n/a
10	ATF2	chr15:77306056-77307216	GM12878	blood:	n/a	n/a
11	ATF2	chr15:77316619-77316962	GM12878	blood:	n/a	n/a
12	ATF2	chr15:77306145-77306892	GM12878	blood:	n/a	n/a
13	ATF2	chr15:77280492-77281189	GM12878	blood:	n/a	n/a
14	ATF2	chr15:77314306-77314560	GM12878	blood:	n/a	n/a
15	ATF2	chr15:77280450-77281122	GM12878	blood:	n/a	n/a
16	ATF3	chr15:77345998-77346388	K562	blood:	n/a	n/a
17	BACH1	chr15:77377554-77377837	K562	blood:	n/a	n/a
18	BACH1	chr15:77363295-77363664	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr15:77320425-77320611	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr15:77362785-77363076	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr15:77280368-77281177	GM12878	blood:	n/a	n/a
22	BATF	chr15:77377687-77378083	GM12878	blood:	n/a	n/a
23	BATF	chr15:77377594-77378131	GM12878	blood:	n/a	n/a
24	BATF	chr15:77290050-77290368	GM12878	blood:	n/a	chr15:77290281-77290290
25	BATF	chr15:77268877-77269183	GM12878	blood:	n/a	n/a
26	BATF	chr15:77280672-77281099	GM12878	blood:	n/a	n/a
27	BATF	chr15:77306056-77306497	GM12878	blood:	n/a	chr15:77306290-77306300 chr15:77306289-77306300 chr15:77306286-77306296
28	BATF	chr15:77312280-77312501	GM12878	blood:	n/a	n/a
29	BATF	chr15:77306094-77306473	GM12878	blood:	n/a	chr15:77306290-77306300 chr15:77306289-77306300 chr15:77306286-77306296
30	BATF	chr15:77290041-77290431	GM12878	blood:	n/a	chr15:77290281-77290290
31	BCL11A	chr15:77280639-77281215	GM12878	blood:	n/a	n/a
32	BCL11A	chr15:77290034-77290413	GM12878	blood:	n/a	chr15:77290214-77290223
33	BCL11A	chr15:77306811-77307122	GM12878	blood:	n/a	n/a
34	BCL11A	chr15:77280649-77281093	GM12878	blood:	n/a	n/a
35	BCL11A	chr15:77306807-77307126	GM12878	blood:	n/a	n/a
36	BCL3	chr15:77319696-77320041	GM12878	blood:	n/a	n/a
37	BCL3	chr15:77359613-77360283	A549	lung:	n/a	n/a
38	BCL3	chr15:77327427-77328043	A549	lung:	n/a	n/a
39	BCL3	chr15:77280656-77281077	GM12878	blood:	n/a	n/a
40	BCL3	chr15:77325651-77326184	A549	lung:	n/a	n/a
41	BCL3	chr15:77326777-77327284	A549	lung:	n/a	n/a
42	BCL3	chr15:77325266-77325980	A549	lung:	n/a	n/a
43	BCL3	chr15:77326463-77328028	A549	lung:	n/a	n/a
44	BCL3	chr15:77319746-77319961	GM12878	blood:	n/a	n/a
45	BCLAF1	chr15:77306496-77307260	GM12878	blood:	n/a	n/a
46	BCLAF1	chr15:77280280-77281228	GM12878	blood:	n/a	n/a
47	BCLAF1	chr15:77265609-77265941	GM12878	blood:	n/a	chr15:77265853-77265861
48	BHLHE40	chr15:77319308-77319431	K562	blood:	n/a	n/a
49	BHLHE40	chr15:77290077-77290411	GM12878	blood:	n/a	n/a
50	BHLHE40	chr15:77312372-77312424	GM12878	blood:	n/a	n/a

(count:2570 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:77287762-77287812	AG10803	skin:	n/a
2	chr15:77320787-77320837	NH-A	brain:	n/a
3	chr15:77287762-77287812	NHDF-neo	bronchial:	n/a
4	chr15:77376250-77376300	T-47D	breast:	n/a
5	chr15:77323565-77323615	HL-60	blood:	n/a
6	chr15:77324758-77324808	Hepatocyte	liver:	n/a
7	chr15:77320672-77320722	MCF-7	breast:	n/a
8	chr15:77324526-77324576	IMR90	lung:	fetal
9	chr15:77287762-77287812	AG10803	skin:	n/a
10	chr15:77320787-77320837	NH-A	brain:	n/a
11	chr15:77287762-77287812	NHDF-neo	bronchial:	n/a
12	chr15:77376250-77376300	T-47D	breast:	n/a
13	chr15:77323565-77323615	HL-60	blood:	n/a
14	chr15:77324758-77324808	Hepatocyte	liver:	n/a
15	chr15:77320672-77320722	MCF-7	breast:	n/a
16	chr15:77324526-77324576	IMR90	lung:	fetal
17	chr15:77324758-77324808	ProgFib	skin:	n/a
18	chr15:77359477-77359527	AG09309	skin:	n/a
19	chr15:77324751-77324801	Hela-S3	cervix:	n/a
20	chr15:77376235-77376285	GM19239	blood:	n/a
21	chr15:77364890-77364940	HEK293	kidney:	embryo
22	chr15:77363627-77363677	HAEpiC	amniotic membrane:	n/a
23	chr15:77364519-77364569	SK-N-SH	brain:	n/a
24	chr15:77336938-77336988	SK-N-SH_RA	brain:	n/a
25	chr15:77364519-77364569	GM06990	blood:	n/a
26	chr15:77364801-77364851	PrEC	prostate:	n/a
27	chr15:77324751-77324801	HCT-116	colon:	n/a
28	chr15:77287345-77287395	PrEC	prostate:	n/a
29	chr15:77348431-77348481	U87	brain:	n/a
30	chr15:77363627-77363677	MCF-7	breast:	n/a
31	chr15:77336938-77336988	HL-60	blood:	n/a
32	chr15:77363299-77363349	HRPEpiC	eye:	n/a
33	chr15:77287243-77287293	ovcar-3	ovarian:	n/a
34	chr15:77320787-77320837	PrEC	prostate:	n/a
35	chr15:77286948-77286998	Caco-2	colon:	n/a
36	chr15:77327887-77327937	ECC-1	luminal epithelium:	n/a
37	chr15:77350049-77350099	HNPCEpiC	eye:	n/a
38	chr15:77364890-77364940	MCF-7	breast:	n/a
39	chr15:77364801-77364851	LNCaP	prostate:	n/a
40	chr15:77363627-77363677	A549	lung:	n/a
41	chr15:77359477-77359527	NHDF-neo	bronchial:	n/a
42	chr15:77287899-77287949	HCPEpiC	choroid plexus:	n/a
43	chr15:77359477-77359527	HCF	heart:	n/a
44	chr15:77348431-77348481	A549	lung:	n/a
45	chr15:77320787-77320837	HEEpiC	esophagus:	n/a
46	chr15:77287762-77287812	HL-60	blood:	n/a
47	chr15:77347405-77347455	HCPEpiC	choroid plexus:	n/a
48	chr15:77363192-77363242	GM12891	blood:	n/a
49	chr15:77323565-77323615	HPAEpiC	pulmonary alveolar:	n/a
50	chr15:77271730-77271780	SK-N-SH	brain:	n/a

(count:110 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:77283310..77284980-chr15:77285061..77287100,2	MCF-7	breast:
2	chr15:77357220..77360797-chr15:77361367..77364060,6	MCF-7	breast:
3	chr15:77257686..77261263-chr15:77264226..77266694,3	K562	blood:
4	chr15:77327656..77329511-chr15:77332033..77335172,3	K562	blood:
5	chr15:77303183..77305636-chr15:77307103..77311098,3	K562	blood:
6	chr15:77259410..77261761-chr15:77265771..77267804,2	MCF-7	breast:
7	chr15:77366731..77368356-chr15:77373004..77374845,2	K562	blood:
8	chr15:77341652..77343382-chr15:77361893..77364466,3	K562	blood:
9	chr15:77257244..77258840-chr15:77260404..77262433,2	K562	blood:
10	chr15:77326257..77328074-chr15:77358170..77359996,2	K562	blood:
11	chr15:77338226..77340379-chr15:77349615..77351544,2	K562	blood:
12	chr15:77334559..77338244-chr15:77361377..77364599,4	K562	blood:
13	chr15:77346695..77349657-chr15:77355266..77357615,2	MCF-7	breast:
14	chr15:77254684..77256252-chr15:77267880..77270200,2	K562	blood:
15	chr15:77259410..77261761-chr15:77265771..77267804,2	MCF-7	breast:
16	chr15:77316351..77317289-chr15:77788854..77789825,3	K562	blood:
17	chr15:77195708..77198409-chr15:77360659..77363583,2	K562	blood:
18	chr15:77358882..77364790-chr15:77365543..77372289,11	K562	blood:
19	chr15:77340819..77342632-chr15:77355039..77357924,2	K562	blood:
20	chr15:77361764..77363824-chr15:77378016..77379591,2	MCF-7	breast:
21	chr15:77327656..77330194-chr15:77332164..77335172,3	K562	blood:
22	chr15:77283555..77285967-chr15:77287143..77289785,2	K562	blood:
23	chr15:77334559..77338244-chr15:77361377..77364599,4	K562	blood:
24	chr15:77372560..77374452-chr15:77380766..77383078,2	K562	blood:
25	chr15:77352302..77353897-chr15:77355148..77357991,2	MCF-7	breast:
26	chr15:77319827..77321678-chr15:77343496..77345800,2	MCF-7	breast:
27	chr15:77362106..77364633-chr15:77375983..77377903,3	MCF-7	breast:
28	chr15:77316659..77317287-chr15:77410867..77411851,3	MCF-7	breast:
29	chr15:77357220..77360797-chr15:77361367..77364060,6	MCF-7	breast:
30	chr15:77282963..77284982-chr15:77290568..77292460,2	K562	blood:
31	chr15:76630323..76632934-chr15:77355490..77357171,2	K562	blood:
32	chr15:77265440..77266266-chr15:77305789..77306421,2	MCF-7	breast:
33	chr15:77282963..77284982-chr15:77290568..77292460,2	K562	blood:
34	chr15:77343568..77346165-chr15:77350645..77352262,2	K562	blood:
35	chr15:77265440..77266266-chr15:77305789..77306421,2	MCF-7	breast:
36	chr12:52607550..52609312-chr15:77270485..77271990,2	MCF-7	breast:
37	chr15:77280526..77282215-chr15:77292098..77294137,2	K562	blood:
38	chr15:77240619..77242509-chr15:77252756..77255459,2	MCF-7	breast:
39	chr15:77257244..77258840-chr15:77260404..77262433,2	K562	blood:
40	chr15:77362899..77363478-chr4:88141336..88142074,2	NB4	blood:
41	chr15:77339779..77342430-chr15:77346063..77348517,2	MCF-7	breast:
42	chr15:77377099..77380194-chr15:77383029..77386419,3	K562	blood:
43	chr15:77336838..77340785-chr15:77352977..77355906,3	K562	blood:
44	chr15:77328280..77330879-chr15:77355103..77356921,2	K562	blood:
45	chr15:77311951..77316312-chr15:77325010..77329080,4	K562	blood:
46	chr15:77305426..77307546-chr15:77319169..77320927,2	K562	blood:
47	chr15:77332598..77335104-chr15:77338074..77339723,2	MCF-7	breast:
48	chr15:77380641..77382728-chr15:77388644..77390863,2	MCF-7	breast:
49	chr15:77336838..77340785-chr15:77352977..77355906,3	K562	blood:
50	chr15:77359065..77361270-chr15:77362713..77364449,3	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSPAN3-1	chr15:77333726-77333740	NONHSAT047418
2	lnc-PEAK1.1-4	chr15:77359996-77360667	ENSG00000269951.1
3	lnc-TSPAN3-1	chr15:77334178-77335144	NONHSAT047418
4	lnc-PEAK1.1-3	chr15:77362209-77362400	NONHSAT047422
5	lnc-TSPAN3-3	chr15:77269258-77269551	NONHSAT047417
6	lnc-PSTPIP1-1	chr15:77336022-77336179	ENSG00000259652.1
7	lnc-TSPAN3-1	chr15:77334178-77335533	ENSG00000260787.1
8	lnc-PSTPIP1-1	chr15:77337397-77337502	ENSG00000259652.1
9	lnc-PEAK1.1-3	chr15:77363234-77363434	NONHSAT047422

No data

Variant related genes	Relation type
ENSG00000260787	TF binding region
TSPAN3	TF binding region
RN7SL278P	TF binding region
PSTPIP1	TF binding region
KRT8P23	TF binding region
ENSG00000269951	TF binding region
ENSG00000259652	TF binding region
ENSG00000260787	CpG island
TSPAN3	CpG island
RN7SL278P	CpG island
PSTPIP1	CpG island
KRT8P23	CpG island
ENSG00000269951	CpG island
ENSG00000259652	CpG island
ENSG00000140368	chromatin interactions
ENSG00000140386	chromatin interactions
ENSG00000140391	chromatin interactions
ENSG00000145332	chromatin interactions
ENSG00000139725	chromatin interactions
ENSG00000260787	chromatin interactions
ENSG00000243365	chromatin interactions
ENSG00000269951	chromatin interactions
ENSG00000212694	chromatin interactions
ENSG00000140374	chromatin interactions
ENSG00000259652	chromatin interactions

Extended variants
information (count: 5129 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:5129 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12148386	chr15:77254544-77254545	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189328070	chr15:77254620-77254621	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs61318775	chr15:77254636-77254637	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs182374736	chr15:77254692-77254693	Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs147993504	chr15:77254693-77254694	Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs543529113	chr15:77254706-77254707	Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs186311159	chr15:77254714-77254715	Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs114125448	chr15:77254744-77254745	Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs114915430	chr15:77254752-77254753	Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs141624581	chr15:77254789-77254790	Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs529288806	chr15:77254799-77254800	Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs554356219	chr15:77254829-77254830	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs550989443	chr15:77254849-77254850	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs537061687	chr15:77254868-77254869	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs569138321	chr15:77254891-77254892	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs371525791	chr15:77254894-77254895	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs372714462	chr15:77254923-77254924	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs115912816	chr15:77254934-77254935	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs376956144	chr15:77254963-77254964	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs555522575	chr15:77254976-77254977	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs573714897	chr15:77255002-77255003	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs111464716	chr15:77255013-77255014	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs191102436	chr15:77255024-77255025	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs2469205	chr15:77255029-77255030	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs542316432	chr15:77255137-77255138	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs566094166	chr15:77255181-77255182	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs533909324	chr15:77255187-77255188	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs150545193	chr15:77255204-77255205	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs532185223	chr15:77255253-77255254	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs542377266	chr15:77255315-77255316	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs555137329	chr15:77255329-77255330	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs138573705	chr15:77255334-77255335	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs182945242	chr15:77255346-77255347	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs550795485	chr15:77255348-77255349	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs76772694	chr15:77255349-77255350	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs533135032	chr15:77255370-77255371	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs552107402	chr15:77255386-77255387	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs79172280	chr15:77255482-77255483	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs186212654	chr15:77255539-77255540	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs551908414	chr15:77255585-77255586	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs114226021	chr15:77255603-77255604	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs537984815	chr15:77255608-77255609	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs559244948	chr15:77255650-77255651	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs374377183	chr15:77255651-77255652	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs371749472	chr15:77255704-77255705	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs577567806	chr15:77255732-77255733	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs538216573	chr15:77255752-77255753	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs114990800	chr15:77255782-77255783	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs573616839	chr15:77255833-77255834	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs191362551	chr15:77255841-77255842	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Acute myeloid leukemia	20962326	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4494 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77224800-77256000	Weak transcription	Pancreas	Pancrea
2	chr15:77225000-77254600	Weak transcription	Aorta	Aorta
3	chr15:77225000-77260200	Weak transcription	Right Ventricle	heart
4	chr15:77225400-77255400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr15:77229400-77255000	Weak transcription	Gastric	stomach
6	chr15:77241400-77256000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr15:77243800-77256000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr15:77243800-77256200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr15:77244000-77256000	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr15:77244000-77256000	Weak transcription	NH-A	brain
11	chr15:77244000-77256800	Weak transcription	Primary T cells from cord blood	blood
12	chr15:77247600-77256200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr15:77252000-77259000	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr15:77252000-77259600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr15:77253000-77255200	Enhancers	Ovary	ovary
16	chr15:77253400-77255000	Enhancers	Skeletal Muscle Male	skeletal muscle
17	chr15:77253400-77256000	Enhancers	Fetal Muscle Leg	muscle
18	chr15:77253600-77256800	Enhancers	Rectal Smooth Muscle	rectum
19	chr15:77253800-77254600	Enhancers	Right Atrium	heart
20	chr15:77253800-77255800	Enhancers	HSMMtube	muscle
21	chr15:77253800-77256000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr15:77254000-77254600	Enhancers	Stomach Smooth Muscle	stomach
23	chr15:77254200-77254800	Enhancers	Adipose Nuclei	Adipose
24	chr15:77254200-77259600	Weak transcription	Brain Anterior Caudate	brain
25	chr15:77254400-77254600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr15:77254400-77254600	Enhancers	Colon Smooth Muscle	Colon
27	chr15:77254400-77254600	Enhancers	GM12878-XiMat	blood
28	chr15:77254400-77255000	Enhancers	Primary B cells from peripheral blood	blood
29	chr15:77254400-77256000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr15:77254400-77256200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr15:77254400-77256200	Enhancers	Left Ventricle	heart
32	chr15:77254400-77256400	Enhancers	Psoas Muscle	Psoas
33	chr15:77254600-77254800	Bivalent/Poised TSS	K562	blood
34	chr15:77254600-77256000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr15:77254600-77256400	Enhancers	Aorta	Aorta
36	chr15:77254600-77259600	Weak transcription	Right Atrium	heart
37	chr15:77254600-77259800	Weak transcription	Stomach Smooth Muscle	stomach
38	chr15:77254800-77256000	Weak transcription	Adipose Nuclei	Adipose
39	chr15:77255000-77255200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr15:77255000-77255200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
41	chr15:77255000-77255200	Enhancers	Gastric	stomach
42	chr15:77255000-77256000	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr15:77255200-77255400	Enhancers	Primary B cells from peripheral blood	blood
44	chr15:77255200-77256000	Weak transcription	Gastric	stomach
45	chr15:77255200-77259400	Weak transcription	Ovary	ovary
46	chr15:77255400-77255600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr15:77255400-77255800	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr15:77255600-77256000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr15:77255800-77256200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
50	chr15:77255800-77256400	Bivalent Enhancer	Fetal Intestine Small	intestine

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