Variant report

Variant	nsv527237
Chromosome Location	chr15:75305040-75321262
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:638)
CpG islands
(count:917)
Chromatin interactive
region (count:52)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:638 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:75315260-75316121	K562	blood:	n/a	n/a
2	ATF2	chr15:75315687-75316148	GM12878	blood:	n/a	n/a
3	ATF2	chr15:75315653-75316175	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr15:75315622-75316204	GM12878	blood:	n/a	n/a
5	ATF2	chr15:75315608-75316216	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr15:75315749-75316347	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr15:75315416-75315594	K562	blood:	n/a	n/a
8	BACH1	chr15:75316330-75316610	K562	blood:	n/a	n/a
9	BCL3	chr15:75315307-75316714	A549	lung:	n/a	chr15:75316029-75316037 chr15:75316004-75316013 chr15:75315791-75315800 chr15:75315838-75315846
10	BCL3	chr15:75315647-75316488	A549	lung:	n/a	chr15:75316029-75316037 chr15:75316004-75316013 chr15:75315791-75315800 chr15:75315838-75315846
11	BCLAF1	chr15:75316372-75316860	GM12878	blood:	n/a	n/a
12	BCLAF1	chr15:75315633-75316306	GM12878	blood:	n/a	chr15:75316029-75316037 chr15:75316004-75316013 chr15:75315791-75315800 chr15:75315838-75315846
13	BCLAF1	chr15:75315693-75316194	GM12878	blood:	n/a	chr15:75316029-75316037 chr15:75316004-75316013 chr15:75315791-75315800 chr15:75315838-75315846
14	BHLHE40	chr15:75315508-75316141	K562	blood:	n/a	n/a
15	BHLHE40	chr15:75315674-75316145	GM12878	blood:	n/a	n/a
16	BHLHE40	chr15:75315706-75316176	HepG2	liver:	n/a	n/a
17	BRCA1	chr15:75315653-75316184	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr15:75315710-75316187	HepG2	liver:	n/a	n/a
19	BRCA1	chr15:75315603-75316556	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr15:75315679-75316186	GM12878	blood:	n/a	n/a
21	CBX3	chr15:75315214-75316158	K562	blood:	n/a	n/a
22	CCNT2	chr15:75315623-75316218	K562	blood:	n/a	n/a
23	CEBPB	chr15:75316398-75316696	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr15:75315716-75316098	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr15:75309884-75310130	K562	blood:	n/a	chr15:75310010-75310027 chr15:75310012-75310023
26	CEBPB	chr15:75316487-75316608	K562	blood:	n/a	n/a
27	CEBPB	chr15:75309908-75310108	IMR90	lung:	n/a	chr15:75310010-75310027 chr15:75310012-75310023
28	CEBPB	chr15:75304808-75305163	K562	blood:	n/a	chr15:75304993-75305002 chr15:75304991-75305004 chr15:75304992-75305003 chr15:75304991-75305002
29	CEBPB	chr15:75304849-75305154	HepG2	liver:	n/a	chr15:75304993-75305002 chr15:75304991-75305004 chr15:75304992-75305003 chr15:75304991-75305002
30	CEBPB	chr15:75304702-75305217	A549	lung:	n/a	chr15:75304993-75305002 chr15:75304991-75305004 chr15:75304992-75305003 chr15:75304991-75305002
31	CEBPB	chr15:75309874-75310137	HepG2	liver:	n/a	chr15:75310010-75310027 chr15:75310012-75310023
32	CEBPB	chr15:75315594-75315973	K562	blood:	n/a	n/a
33	CEBPB	chr15:75304854-75305158	IMR90	lung:	n/a	chr15:75304993-75305002 chr15:75304991-75305004 chr15:75304992-75305003 chr15:75304991-75305002
34	CEBPB	chr15:75309884-75310142	A549	lung:	n/a	chr15:75310010-75310027 chr15:75310012-75310023
35	CEBPB	chr15:75315408-75315925	K562	blood:	n/a	n/a
36	CEBPB	chr15:75304850-75305121	A549	lung:	n/a	chr15:75304993-75305002 chr15:75304991-75305004 chr15:75304992-75305003 chr15:75304991-75305002
37	CEBPB	chr15:75315626-75316589	GM12878	blood:	n/a	n/a
38	CEBPD	chr15:75315185-75316240	K562	blood:	n/a	n/a
39	CEBPD	chr15:75315694-75316164	HepG2	liver:	n/a	n/a
40	CHD1	chr15:75315902-75316458	GM12878	blood:	n/a	n/a
41	CHD1	chr15:75316073-75316415	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr15:75315611-75316688	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr15:75315600-75316317	GM12878	blood:	n/a	n/a
44	CHD2	chr15:75315645-75316273	HepG2	liver:	n/a	n/a
45	CHD2	chr15:75315470-75316396	K562	blood:	n/a	n/a
46	CHD2	chr15:75315634-75316416	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr15:75315668-75316155	ECC-1	luminal epithelium:	n/a	n/a
48	CREB1	chr15:75315665-75316169	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr15:75315697-75316067	A549	lung:	n/a	n/a
50	CREB1	chr15:75315581-75316321	GM12878	blood:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:75315579-75315629	LNCaP	prostate:	n/a
2	chr15:75315724-75315774	HCPEpiC	choroid plexus:	n/a
3	chr15:75315579-75315629	LNCaP	prostate:	n/a
4	chr15:75315724-75315774	HCPEpiC	choroid plexus:	n/a
5	chr15:75307476-75307526	HRCEpiC	kidney:	n/a
6	chr15:75316323-75316373	BE2_C	brain:	n/a
7	chr15:75314761-75314811	HUVEC	blood vessel:	n/a
8	chr15:75315579-75315629	HAEpiC	amniotic membrane:	n/a
9	chr15:75313579-75313629	HEK293	kidney:	embryo
10	chr15:75314761-75314811	HL-60	blood:	n/a
11	chr15:75315747-75315797	SK-N-SH_RA	brain:	n/a
12	chr15:75315747-75315797	HRPEpiC	eye:	n/a
13	chr15:75307476-75307526	HAEpiC	amniotic membrane:	n/a
14	chr15:75314761-75314811	MCF10A-Er-Src	breast:	n/a
15	chr15:75315928-75315978	SKMC	muscle:	n/a
16	chr15:75316240-75316290	CMK	blood:	n/a
17	chr15:75307476-75307526	SK-N-MC	brain:	n/a
18	chr15:75315856-75315906	HCF	heart:	n/a
19	chr15:75315747-75315797	SK-N-MC	brain:	n/a
20	chr15:75316240-75316290	HL-60	blood:	n/a
21	chr15:75316111-75316161	U87	brain:	n/a
22	chr15:75315724-75315774	SKMC	muscle:	n/a
23	chr15:75315928-75315978	HCPEpiC	choroid plexus:	n/a
24	chr15:75307476-75307526	U87	brain:	n/a
25	chr15:75315928-75315978	NHDF-neo	bronchial:	n/a
26	chr15:75316111-75316161	HepG2	liver:	n/a
27	chr15:75316323-75316373	AG04450	lung:	fetal
28	chr15:75315856-75315906	U87	brain:	n/a
29	chr15:75316111-75316161	HUVEC	blood vessel:	n/a
30	chr15:75315724-75315774	HEK293	kidney:	embryo
31	chr15:75313579-75313629	RPTEC	kidney:	n/a
32	chr15:75315928-75315978	SK-N-SH_RA	brain:	n/a
33	chr15:75316240-75316290	Jurkat	blood:	n/a
34	chr15:75315956-75316006	GM12892	blood:	n/a
35	chr15:75315724-75315774	HCM	heart:	n/a
36	chr15:75315874-75315924	AG09309	skin:	n/a
37	chr15:75316240-75316290	HNPCEpiC	eye:	n/a
38	chr15:75319403-75319453	NH-A	brain:	n/a
39	chr15:75313579-75313629	Hepatocyte	liver:	n/a
40	chr15:75315956-75316006	NHBE	bronchial:	n/a
41	chr15:75315956-75316006	MCF10A-Er-Src	breast:	n/a
42	chr15:75315724-75315774	RPTEC	kidney:	n/a
43	chr15:75316323-75316373	HCM	heart:	n/a
44	chr15:75316240-75316290	RPTEC	kidney:	n/a
45	chr15:75315856-75315906	AG04450	lung:	fetal
46	chr15:75314761-75314811	HAEpiC	amniotic membrane:	n/a
47	chr15:75316323-75316373	NH-A	brain:	n/a
48	chr15:75316111-75316161	HAEpiC	amniotic membrane:	n/a
49	chr15:75315928-75315978	MCF10A-Er-Src	breast:	n/a
50	chr15:75316323-75316373	H1-hESC	embryonic stem cell:	embryo

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:75315804..75316415-chr5:111093426..111093927,2	NB4	blood:
2	chr1:151512687..151513188-chr15:75315845..75316431,2	Hela-S3	cervix:
3	chr15:75319473..75322181-chr17:62205905..62208887,2	MCF-7	breast:
4	chr15:75315988..75318426-chr15:75334585..75336329,2	K562	blood:
5	chr15:75314427..75332274-chr15:75491598..75502885,56	MCF-7	breast:
6	chr15:75287456..75290010-chr15:75314463..75316098,2	K562	blood:
7	chr15:75315821..75316629-chr6:38670308..38670932,2	Hela-S3	cervix:
8	chr15:75302980..75304655-chr15:75315027..75317604,2	MCF-7	breast:
9	chr15:75287065..75288881-chr15:75303278..75305678,2	MCF-7	breast:
10	chr13:48611622..48612268-chr15:75315982..75316532,2	Hela-S3	cervix:
11	chr15:75307941..75311039-chr15:75492807..75495397,4	MCF-7	breast:
12	chr15:75314438..75320960-chr15:75334023..75339188,6	K562	blood:
13	chr15:75316439..75318954-chr15:75442453..75445329,2	K562	blood:
14	chr15:75299758..75302262-chr15:75305323..75307805,2	K562	blood:
15	chr15:75247469..75252493-chr15:75314645..75318771,7	MCF-7	breast:
16	chr15:75316003..75319633-chr15:75325409..75329451,5	MCF-7	breast:
17	chr11:62431893..62432696-chr15:75315867..75316629,2	Hela-S3	cervix:
18	chr15:75249504..75251132-chr15:75306617..75309149,2	MCF-7	breast:
19	chr15:75304706..75307905-chr15:75494120..75496489,3	MCF-7	breast:
20	chr15:75316867..75318427-chr15:75489096..75491269,2	K562	blood:
21	chr15:75306128..75307779-chr15:75522303..75524360,2	MCF-7	breast:
22	chr15:75315895..75316445-chr6:26217044..26217706,2	Hela-S3	cervix:
23	chr15:75304775..75307425-chr15:75315753..75317450,2	MCF-7	breast:
24	chr15:75315116..75318130-chr15:75502238..75505511,3	K562	blood:
25	chr15:75320338..75322055-chr15:75659198..75660857,2	K562	blood:
26	chr15:75315711..75316297-chr9:131940036..131940688,2	Hela-S3	cervix:
27	chr15:75320936..75323384-chr15:75742999..75744813,2	K562	blood:
28	chr15:75314737..75326433-chr15:75490770..75500610,30	K562	blood:
29	chr15:75197976..75200333-chr15:75311534..75313971,2	MCF-7	breast:
30	chr15:75313706..75315834-chr15:75659150..75661879,2	K562	blood:
31	chr15:75227655..75229943-chr15:75305697..75307723,2	MCF-7	breast:
32	chr15:75248156..75250138-chr15:75312985..75314621,2	K562	blood:
33	chr15:75300826..75305111-chr15:75313603..75318752,6	MCF-7	breast:
34	chr15:75315622..75316343-chrX:53710851..53711547,2	Hela-S3	cervix:
35	chr15:75286200..75292858-chr15:75303462..75309796,11	MCF-7	breast:
36	chr15:75287417..75289225-chr15:75314885..75317439,2	MCF-7	breast:
37	chr15:75289096..75291038-chr15:75311135..75313518,2	K562	blood:
38	chr15:75163895..75166026-chr15:75315159..75317542,2	MCF-7	breast:
39	chr15:75312886..75327225-chr15:75491522..75500922,36	K562	blood:
40	chr15:75249439..75250408-chr15:75315837..75316367,2	Hela-S3	cervix:
41	chr15:75312974..75314545-chr15:75319441..75321661,2	K562	blood:
42	chr15:75316059..75318846-chr15:75482061..75483763,2	K562	blood:
43	chr15:75320623..75324392-chr15:75326315..75329283,4	K562	blood:
44	chr15:75286466..75289268-chr15:75313854..75316191,2	MCF-7	breast:
45	chr11:119177443..119177955-chr15:75319985..75320485,2	NB4	blood:
46	chr15:75318584..75321988-chr15:75334747..75339188,4	K562	blood:
47	chr15:75300826..75305111-chr15:75313603..75318752,6	MCF-7	breast:
48	chr15:75317681..75319554-chr15:75468092..75469844,2	MCF-7	breast:
49	chr15:75314704..75323577-chr15:75491522..75500562,29	MCF-7	breast:
50	chr15:75246752..75249656-chr15:75313121..75316891,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPCDC-2	chr15:75315321-75315597	NONHSAT047286
2	lnc-PPCDC-4	chr15:75305018-75305146	NONHSAT047284
3	lnc-PPCDC-4	chr15:75310211-75310287	NONHSAT047284
4	lnc-SCAMP5-2	chr15:75315941-75315967	NONHSAT047287

No data

Variant related genes	Relation type
ENSG00000260483	TF binding region
PPCDC	TF binding region
SCAMP5	TF binding region
ENSG00000260483	CpG island
PPCDC	CpG island
SCAMP5	CpG island
ENSG00000178761	chromatin interactions
ENSG00000140497	chromatin interactions
ENSG00000138621	chromatin interactions
ENSG00000136143	chromatin interactions
ENSG00000260274	chromatin interactions
ENSG00000134986	chromatin interactions
ENSG00000178607	chromatin interactions
ENSG00000168274	chromatin interactions
ENSG00000143367	chromatin interactions
ENSG00000261779	chromatin interactions
ENSG00000255432	chromatin interactions
ENSG00000086758	chromatin interactions
ENSG00000188483	chromatin interactions
ENSG00000178718	chromatin interactions
ENSG00000162194	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000198794	chromatin interactions
ENSG00000260483	chromatin interactions
ENSG00000140400	chromatin interactions
ENSG00000136159	chromatin interactions
ENSG00000167173	chromatin interactions
ENSG00000169375	chromatin interactions
ENSG00000124767	chromatin interactions

Extended variants
information (count: 605 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:605 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7174129	chr15:75305040-75305041	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544124213	chr15:75305055-75305056	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
3	rs374460253	chr15:75305057-75305058	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
4	rs60910940	chr15:75305058-75305059	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs371182880	chr15:75305074-75305075	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
6	rs12908445	chr15:75305114-75305115	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs374045413	chr15:75305125-75305126	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
8	rs368193195	chr15:75305126-75305127	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
9	rs200339367	chr15:75305167-75305168	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs143481943	chr15:75305172-75305173	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs375634785	chr15:75305184-75305185	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs566494507	chr15:75305202-75305203	Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs527259577	chr15:75305204-75305205	Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs7342649	chr15:75305216-75305217	Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs376265011	chr15:75305307-75305308	Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs146757178	chr15:75305311-75305312	Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs7342650	chr15:75305330-75305331	Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs556520937	chr15:75305331-75305332	Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs191726917	chr15:75305372-75305373	Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs145995296	chr15:75305378-75305379	Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs565252067	chr15:75305430-75305431	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs538777067	chr15:75305489-75305490	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs141177629	chr15:75305496-75305497	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs572116174	chr15:75305507-75305508	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs542607824	chr15:75305514-75305515	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs145005881	chr15:75305573-75305574	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs117130875	chr15:75305635-75305636	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs183140174	chr15:75305666-75305667	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs371457589	chr15:75305736-75305737	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs555184708	chr15:75305740-75305741	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs187254573	chr15:75305789-75305790	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs138776365	chr15:75305790-75305791	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs542500836	chr15:75305817-75305818	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs533130808	chr15:75305847-75305848	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs189672246	chr15:75305867-75305868	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs6495139	chr15:75305931-75305932	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs377329613	chr15:75305978-75305979	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs550258733	chr15:75305992-75305993	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs148949074	chr15:75306033-75306034	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs6495140	chr15:75306041-75306042	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs143728929	chr15:75306058-75306059	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs148136957	chr15:75306079-75306080	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs550039509	chr15:75306139-75306140	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs60597882	chr15:75306176-75306177	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs569601124	chr15:75306224-75306225	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs17421513	chr15:75306264-75306265	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs553851370	chr15:75306278-75306279	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs182337044	chr15:75306281-75306282	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs186959478	chr15:75306304-75306305	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs554700070	chr15:75306361-75306362	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
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
small cell lung cancer	20016488	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
Congenital diaphragmatic hernia	21085971	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Epilepsy	22083797	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:786 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75289000-75315800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:75289400-75305600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr15:75289400-75315400	Weak transcription	Fetal Kidney	kidney
4	chr15:75289600-75305400	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr15:75290000-75309400	Weak transcription	Gastric	stomach
6	chr15:75290000-75316000	Weak transcription	Small Intestine	intestine
7	chr15:75291400-75305400	Weak transcription	Fetal Brain Male	brain
8	chr15:75292600-75305400	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr15:75293200-75315800	Weak transcription	Duodenum Mucosa	Duodenum
10	chr15:75294600-75312200	Weak transcription	Adipose Nuclei	Adipose
11	chr15:75294600-75315600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr15:75298200-75305600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr15:75300400-75312200	Weak transcription	Spleen	Spleen
14	chr15:75301000-75315400	Weak transcription	Thymus	Thymus
15	chr15:75301800-75306600	Weak transcription	Placenta	Placenta
16	chr15:75302000-75314000	Strong transcription	Fetal Intestine Small	intestine
17	chr15:75302200-75313200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr15:75302200-75313400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr15:75303400-75305200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr15:75303600-75309800	Strong transcription	Brain Germinal Matrix	brain
21	chr15:75303600-75313800	Strong transcription	Cortex derived primary cultured neurospheres	brain
22	chr15:75303800-75309400	Strong transcription	Brain Cingulate Gyrus	brain
23	chr15:75303800-75313800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr15:75303800-75314000	Strong transcription	Fetal Brain Female	brain
25	chr15:75304000-75306800	Strong transcription	Fetal Intestine Large	intestine
26	chr15:75304000-75306800	Strong transcription	Pancreas	Pancrea
27	chr15:75304000-75307600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr15:75304000-75308800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
29	chr15:75304000-75309400	Strong transcription	Brain Hippocampus Middle	brain
30	chr15:75304000-75309400	Strong transcription	Brain Inferior Temporal Lobe	brain
31	chr15:75304000-75315800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr15:75304000-75316000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
33	chr15:75304200-75307400	Strong transcription	H9 Cell Line	embryonic stem cell
34	chr15:75304200-75310000	Weak transcription	Fetal Muscle Trunk	muscle
35	chr15:75304400-75306000	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr15:75304400-75307000	Strong transcription	HepG2	liver
37	chr15:75304400-75307400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
38	chr15:75304400-75313600	Strong transcription	Fetal Stomach	stomach
39	chr15:75304600-75306000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
40	chr15:75304600-75313200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr15:75304800-75306800	Strong transcription	H1 Cell Line	embryonic stem cell
42	chr15:75304800-75310200	Strong transcription	Brain Angular Gyrus	brain
43	chr15:75304800-75312600	Strong transcription	Brain Anterior Caudate	brain
44	chr15:75304800-75314000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr15:75305000-75305400	Strong transcription	HUES6 Cell Line	embryonic stem cell
46	chr15:75305000-75306000	Strong transcription	Brain Substantia Nigra	brain
47	chr15:75305000-75306600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr15:75305000-75307600	Strong transcription	HUES48 Cell Line	embryonic stem cell
49	chr15:75305000-75315800	Weak transcription	Right Ventricle	heart
50	chr15:75305200-75305400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin

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