Variant report

Variant	nsv904552
Chromosome Location	chr15:99954278-99982447
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:520)
CpG islands
(count:1344)
Chromatin interactive
region (count:40)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:520 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:99961418-99962008	HepG2	liver:	n/a	n/a
2	ATF2	chr15:99965347-99965754	GM12878	blood:	n/a	n/a
3	BATF	chr15:99965364-99965661	GM12878	blood:	n/a	chr15:99965442-99965451
4	BHLHE40	chr15:99973687-99973691	GM12878	blood:	n/a	n/a
5	BHLHE40	chr15:99965453-99965469	K562	blood:	n/a	n/a
6	BHLHE40	chr15:99961440-99962002	HepG2	liver:	n/a	n/a
7	BRCA1	chr15:99975665-99975680	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr15:99961492-99961572	IMR90	lung:	n/a	n/a
9	CEBPB	chr15:99961470-99961726	MCF-7	breast:	n/a	n/a
10	CEBPB	chr15:99961467-99961647	HepG2	liver:	n/a	n/a
11	CEBPB	chr15:99965381-99965715	IMR90	lung:	n/a	n/a
12	CEBPB	chr15:99965407-99965607	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr15:99961370-99961725	HepG2	liver:	n/a	n/a
14	CEBPB	chr15:99961361-99961734	HepG2	liver:	n/a	n/a
15	CEBPD	chr15:99961442-99961604	HepG2	liver:	n/a	n/a
16	CHD2	chr15:99965573-99965713	Hela-S3	cervix:	n/a	n/a
17	CHD2	chr15:99975690-99975908	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr15:99973825-99973857	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr15:99973694-99973933	GM12878	blood:	n/a	n/a
20	CHD2	chr15:99961599-99961785	HepG2	liver:	n/a	n/a
21	CHD2	chr15:99961572-99961672	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr15:99966206-99966443	GM12878	blood:	n/a	n/a
23	CTCF	chr15:99966260-99966410	HepG2	liver:	n/a	n/a
24	CTCF	chr15:99973400-99973550	GM12875	blood:	n/a	n/a
25	CTCF	chr15:99966280-99966430	BE2_C	brain:	n/a	n/a
26	CTCF	chr15:99973360-99973510	GM12872	blood:	n/a	n/a
27	CTCF	chr15:99973300-99973450	GM12867	blood:	n/a	n/a
28	CTCF	chr15:99966240-99966390	HCPEpiC	choroid plexus:	n/a	n/a
29	CTCF	chr15:99966260-99966410	HMF	breast:	n/a	n/a
30	CTCF	chr15:99965620-99965770	HRE	kidney:	n/a	n/a
31	CTCF	chr15:99966260-99966410	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr15:99966240-99966390	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr15:99966340-99966490	HFF-Myc	foreskin:	n/a	n/a
34	CTCF	chr15:99966260-99966410	HCT-116	colon:	n/a	n/a
35	CTCF	chr15:99966300-99966450	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr15:99966260-99966410	AG04449	skin:	n/a	n/a
37	CTCF	chr15:99966242-99966386	GM12891	blood:	n/a	n/a
38	CTCF	chr15:99966241-99966460	A549	lung:	n/a	n/a
39	CTCF	chr15:99975580-99975730	NHEK	skin:	n/a	n/a
40	CTCF	chr15:99973260-99973410	GM12866	blood:	n/a	n/a
41	CTCF	chr15:99965818-99965869	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr15:99966218-99966397	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr15:99966237-99966402	Gliobla	brain:	n/a	n/a
44	CTCF	chr15:99971380-99971530	HepG2	liver:	n/a	chr15:99971424-99971445 chr15:99971429-99971447
45	CTCF	chr15:99966260-99966410	GM12872	blood:	n/a	n/a
46	CTCF	chr15:99966240-99966390	HVMF	connective:	n/a	n/a
47	CTCF	chr15:99966190-99966442	MCF-7	breast:	n/a	n/a
48	CTCF	chr15:99966200-99966350	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr15:99966200-99966350	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr15:99966120-99966270	HRPEpiC	eye:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:99978986-99979036	H1-hESC	embryonic stem cell:	embryo
2	chr15:99979013-99979063	SK-N-SH_RA	brain:	n/a
3	chr15:99978986-99979036	H1-hESC	embryonic stem cell:	embryo
4	chr15:99979013-99979063	SK-N-SH_RA	brain:	n/a
5	chr15:99978986-99979036	MCF-7	breast:	n/a
6	chr15:99971329-99971379	ProgFib	skin:	n/a
7	chr15:99979290-99979340	HIPEpiC	eye:	n/a
8	chr15:99966968-99967018	ProgFib	skin:	n/a
9	chr15:99971423-99971473	SKMC	muscle:	n/a
10	chr15:99975470-99975520	HRCEpiC	kidney:	n/a
11	chr15:99979584-99979634	HCPEpiC	choroid plexus:	n/a
12	chr15:99971329-99971379	GM12878	blood:	n/a
13	chr15:99971213-99971263	SK-N-SH	brain:	n/a
14	chr15:99974881-99974931	HCM	heart:	n/a
15	chr15:99975141-99975191	PFSK-1	brain:	n/a
16	chr15:99971329-99971379	AG04450	lung:	fetal
17	chr15:99975334-99975384	Hela-S3	cervix:	n/a
18	chr15:99979584-99979634	H1-hESC	embryonic stem cell:	embryo
19	chr15:99979346-99979396	HNPCEpiC	eye:	n/a
20	chr15:99979290-99979340	GM12891	blood:	n/a
21	chr15:99979059-99979109	HIPEpiC	eye:	n/a
22	chr15:99979527-99979577	HCF	heart:	n/a
23	chr15:99975010-99975060	HNPCEpiC	eye:	n/a
24	chr15:99975010-99975060	HCPEpiC	choroid plexus:	n/a
25	chr15:99979389-99979439	HNPCEpiC	eye:	n/a
26	chr15:99979389-99979439	NB4	blood:	n/a
27	chr15:99979346-99979396	GM12892	blood:	n/a
28	chr15:99971329-99971379	SK-N-SH	brain:	n/a
29	chr15:99975141-99975191	AG09319	gingival:	n/a
30	chr15:99975010-99975060	HMEC	breast:	n/a
31	chr15:99966833-99966883	SK-N-SH_RA	brain:	n/a
32	chr15:99979584-99979634	HCF	heart:	n/a
33	chr15:99971213-99971263	AG04450	lung:	fetal
34	chr15:99974369-99974419	GM19239	blood:	n/a
35	chr15:99974332-99974382	AG10803	skin:	n/a
36	chr15:99971329-99971379	PrEC	prostate:	n/a
37	chr15:99975470-99975520	ovcar-3	ovarian:	n/a
38	chr15:99967055-99967105	GM19239	blood:	n/a
39	chr15:99979584-99979634	Hepatocyte	liver:	n/a
40	chr15:99975310-99975360	GM12878	blood:	n/a
41	chr15:99979527-99979577	GM06990	blood:	n/a
42	chr15:99966833-99966883	Hepatocyte	liver:	n/a
43	chr15:99975310-99975360	BJ	skin:	n/a
44	chr15:99974332-99974382	IMR90	lung:	fetal
45	chr15:99979346-99979396	AoSMC	blood vessel:	n/a
46	chr15:99975010-99975060	ovcar-3	ovarian:	n/a
47	chr15:99979059-99979109	LNCaP	prostate:	n/a
48	chr15:99979346-99979396	HepG2	liver:	n/a
49	chr15:99974369-99974419	ProgFib	skin:	n/a
50	chr15:99974369-99974419	HPAEpiC	pulmonary alveolar:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:99951575..99954227-chr15:99954620..99956790,2	K562	blood:
2	chr15:99960211..99963086-chr15:99964919..99968237,3	MCF-7	breast:
3	chr15:99963793..99965594-chr15:99976352..99978718,2	K562	blood:
4	chr15:99966071..99969014-chr15:100104345..100107384,3	MCF-7	breast:
5	chr15:99974033..99977897-chr15:99978912..99982934,5	K562	blood:
6	chr15:99972394..99975109-chr15:99977541..99980166,2	MCF-7	breast:
7	chr15:99960211..99963086-chr15:99964919..99968237,3	MCF-7	breast:
8	chr15:99962979..99964880-chr15:99972892..99975204,2	MCF-7	breast:
9	chr15:99947710..99950479-chr15:99955909..99957738,2	MCF-7	breast:
10	chr15:99975615..99977769-chr15:99978276..99979849,2	MCF-7	breast:
11	chr15:99966102..99966691-chr15:100044817..100045390,2	MCF-7	breast:
12	chr15:99949149..99950707-chr15:99953216..99956210,2	MCF-7	breast:
13	chr15:99981264..99984715-chr15:99985641..99987973,4	MCF-7	breast:
14	chr15:99966031..99966539-chr15:100044729..100045649,2	MCF-7	breast:
15	chr15:99972525..99976931-chr15:99986719..99991606,5	MCF-7	breast:
16	chr15:99974033..99977897-chr15:99978912..99982934,5	K562	blood:
17	chr15:99965407..99967484-chr15:99969675..99971240,2	K562	blood:
18	chr15:99979674..99981771-chr15:99994725..99997256,2	K562	blood:
19	chr15:99963793..99965594-chr15:99976352..99978718,2	K562	blood:
20	chr15:99975316..99977266-chr15:99981293..99982934,2	K562	blood:
21	chr15:99949082..99949796-chr15:99965826..99966399,2	MCF-7	breast:
22	chr15:99960171..99963200-chr15:100104719..100108193,3	MCF-7	breast:
23	chr15:99965843..99966811-chr15:100243795..100245106,3	MCF-7	breast:
24	chr15:99975316..99977266-chr15:99981293..99982934,2	K562	blood:
25	chr15:99964977..99967345-chr15:100103742..100106400,3	MCF-7	breast:
26	chr15:99981781..99983657-chr15:100018041..100019744,2	MCF-7	breast:
27	chr15:99962979..99964880-chr15:99972892..99975204,2	MCF-7	breast:
28	chr15:99976374..99976897-chr15:100105314..100105862,2	Hela-S3	cervix:
29	chr15:99966023..99966782-chr15:100243828..100244741,2	MCF-7	breast:
30	chr15:99971316..99975999-chr15:100104042..100107403,7	MCF-7	breast:
31	chr15:99977572..99979807-chr15:99980072..99982815,2	K562	blood:
32	chr15:99972394..99975109-chr15:99977541..99980166,2	MCF-7	breast:
33	chr15:99973224..99976448-chr15:99991050..99995157,5	MCF-7	breast:
34	chr15:99962601..99965549-chr15:100104653..100107115,3	MCF-7	breast:
35	chr15:99975615..99977769-chr15:99978276..99979849,2	MCF-7	breast:
36	chr15:99976307..99978594-chr15:100018036..100019822,2	MCF-7	breast:
37	chr15:99977572..99979807-chr15:99980072..99982815,2	K562	blood:
38	chr15:99981180..99982961-chr15:99993073..99995315,2	MCF-7	breast:
39	chr15:99979583..99981872-chr15:99983556..99985309,2	MCF-7	breast:
40	chr15:99952846..99955288-chr15:100271943..100274389,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTC23-5	chr15:99961346-99963761	l_1247_chr15:99961345-99972053_liver
2	lnc-TTC23-5	chr15:99971261-99971500	l_1247_chr15:99961345-99972053_liver
3	lnc-TTC23-5	chr15:99964546-99965708	l_1247_chr15:99961345-99972053_liver
4	lnc-TTC23-3	chr15:99967214-99967407	ENSG00000259341.1
5	lnc-TTC23-3	chr15:99971033-99971233	ENSG00000259341.1
6	lnc-TTC23-5	chr15:99971676-99972112	l_1247_chr15:99961345-99972053_liver

No data

Variant related genes	Relation type
ENSG00000259341	TF binding region
ENSG00000259341	CpG island
ENSG00000259341	chromatin interactions
ENSG00000183060	chromatin interactions
ENSG00000068305	chromatin interactions

Extended variants
information (count: 1301 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1301 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4965485	chr15:99954278-99954279	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs538519105	chr15:99954306-99954307	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs550234302	chr15:99954310-99954311	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs201414902	chr15:99954311-99954312	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs539145467	chr15:99954406-99954407	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs568833130	chr15:99954408-99954409	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs370665850	chr15:99954418-99954419	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs553933741	chr15:99954434-99954435	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs180680060	chr15:99954436-99954437	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs537657143	chr15:99954437-99954438	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs74640037	chr15:99954475-99954476	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs75612230	chr15:99954476-99954477	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs533793213	chr15:99954479-99954480	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs555120668	chr15:99954484-99954485	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs573630120	chr15:99954494-99954495	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs185713670	chr15:99954561-99954562	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs555643888	chr15:99954562-99954563	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs562164423	chr15:99954568-99954569	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs577517855	chr15:99954573-99954574	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs545099172	chr15:99954595-99954596	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs560032847	chr15:99954606-99954607	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs527380903	chr15:99954608-99954609	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs549629419	chr15:99954611-99954612	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs117885848	chr15:99954618-99954619	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs201587700	chr15:99954659-99954660	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs561451613	chr15:99954706-99954707	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs532059472	chr15:99954757-99954758	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs190337259	chr15:99954793-99954794	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs571623964	chr15:99954837-99954838	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs538697006	chr15:99954842-99954843	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs547767258	chr15:99954866-99954867	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs11853695	chr15:99954867-99954868	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs536328363	chr15:99954885-99954886	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs370162768	chr15:99954913-99954914	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs181744867	chr15:99954934-99954935	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs573472139	chr15:99954941-99954942	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs35443535	chr15:99955010-99955011	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs56280996	chr15:99955022-99955023	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs556001603	chr15:99955071-99955072	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs34326251	chr15:99955098-99955099	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs577861233	chr15:99955099-99955100	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs143855584	chr15:99955123-99955124	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs560074049	chr15:99955138-99955139	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs572080805	chr15:99955144-99955145	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs542710540	chr15:99955156-99955157	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs561489792	chr15:99955158-99955159	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs146877862	chr15:99955164-99955165	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs139728599	chr15:99955186-99955187	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs557448561	chr15:99955217-99955218	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs565484969	chr15:99955296-99955297	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Intellectual disability	22102821	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	21147756	CNVD
Hepatocellular carcinoma	16750200	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	20811773	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Emphysema	19352772	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17142309	CNVD
Schizophrenia	23813976	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:99944800-99972400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr15:99945000-99954600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:99949400-99954400	Weak transcription	HMEC	breast
4	chr15:99949600-99954800	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr15:99949600-99956400	Weak transcription	HepG2	liver
6	chr15:99949800-99954600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr15:99950000-99954600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr15:99950000-99954600	Weak transcription	Esophagus	oesophagus
9	chr15:99950000-99964800	Weak transcription	Adipose Nuclei	Adipose
10	chr15:99950200-99954600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr15:99950200-99955000	Weak transcription	Left Ventricle	heart
12	chr15:99950200-99956600	Weak transcription	Lung	lung
13	chr15:99950200-99956800	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr15:99950800-99965800	Weak transcription	Aorta	Aorta
15	chr15:99951000-99956800	Weak transcription	Right Atrium	heart
16	chr15:99951000-99965200	Weak transcription	Spleen	Spleen
17	chr15:99951600-99954800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr15:99951600-99955600	Weak transcription	Fetal Heart	heart
19	chr15:99953000-99965400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr15:99953200-99954600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr15:99953200-99955000	Weak transcription	Right Ventricle	heart
22	chr15:99954200-99955800	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr15:99954400-99955600	Enhancers	HMEC	breast
24	chr15:99954600-99954800	Enhancers	Esophagus	oesophagus
25	chr15:99954600-99955400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr15:99954600-99955400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr15:99954600-99955600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr15:99954600-99955600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr15:99954600-99955600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr15:99954600-99955600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr15:99954800-99955000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr15:99954800-99955600	Weak transcription	Esophagus	oesophagus
33	chr15:99954800-99955600	Enhancers	Placenta Amnion	Placenta Amnion
34	chr15:99954800-99957200	Enhancers	Placenta	Placenta
35	chr15:99955000-99955600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr15:99955000-99955600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr15:99955000-99955600	Enhancers	Left Ventricle	heart
38	chr15:99955000-99955600	Enhancers	Right Ventricle	heart
39	chr15:99955000-99956200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr15:99955200-99955400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr15:99955200-99955600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr15:99955200-99955600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr15:99955200-99955800	Enhancers	Fetal Muscle Leg	muscle
44	chr15:99955200-99956200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
45	chr15:99955200-99957200	Enhancers	Fetal Stomach	stomach
46	chr15:99955400-99956600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr15:99955400-99964200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr15:99955600-99955800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr15:99955600-99956400	Enhancers	Esophagus	oesophagus
50	chr15:99955600-99956600	Weak transcription	Placenta Amnion	Placenta Amnion

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