Variant report

Variant	rs2304903
Chromosome Location	chr15:75315778-75315779
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOXM1	chr15:75315693-75316247	GM12878	blood:	n/a	n/a
2	CCNT2	chr15:75315623-75316218	K562	blood:	n/a	n/a
3	ELF1	chr15:75315536-75316051	K562	blood:	n/a	chr15:75316003-75316012
4	POLR2A	chr15:75315631-75316868	PANC-1	pancreas:	n/a	n/a
5	TAL1	chr15:75315178-75316216	K562	blood:	n/a	chr15:75315690-75315708 chr15:75315331-75315339
6	POLR2A	chr15:75315719-75316900	GM12878	blood:	n/a	n/a
7	MAX	chr15:75315608-75316715	A549	lung:	n/a	chr15:75315975-75315985 chr15:75316627-75316642
8	POLR2A	chr15:75315597-75316664	SK-N-SH	brain:	n/a	n/a
9	MAX	chr15:75315665-75316217	SK-N-SH	brain:	n/a	chr15:75315975-75315985
10	ZC3H11A	chr15:75315385-75316062	K562	blood:	n/a	n/a
11	SIX5	chr15:75315530-75316112	A549	lung:	n/a	chr15:75315835-75315844 chr15:75315837-75315846 chr15:75315808-75315817 chr15:75315806-75315815
12	TBL1XR1	chr15:75315534-75316244	K562	blood:	n/a	n/a
13	ZBTB33	chr15:75315706-75316082	HepG2	liver:	n/a	chr15:75315878-75315893 chr15:75315923-75315938
14	ELF1	chr15:75315663-75316299	MCF-7	breast:	n/a	chr15:75316003-75316012
15	POLR2A	chr15:75315673-75316939	GM12892	blood:	n/a	n/a
16	ATF2	chr15:75315687-75316148	GM12878	blood:	n/a	n/a
17	JUND	chr15:75315448-75316190	K562	blood:	n/a	chr15:75315782-75315796
18	POLR2A	chr15:75315662-75316273	K562	blood:	n/a	n/a
19	CHD2	chr15:75315611-75316688	Hela-S3	cervix:	n/a	n/a
20	POLR2A	chr15:75315679-75316778	HL-60	blood:	n/a	n/a
21	POLR2A	chr15:75315740-75316807	GM12891	blood:	n/a	n/a
22	USF1	chr15:75315681-75316036	SK-N-SH_RA	brain:	n/a	n/a
23	GTF2F1	chr15:75315646-75316583	Hela-S3	cervix:	n/a	n/a
24	IRF1	chr15:75315670-75316068	K562	blood:	n/a	n/a
25	HEY1	chr15:75315492-75316240	HepG2	liver:	n/a	n/a
26	YY1	chr15:75315655-75316243	SK-N-SH_RA	brain:	n/a	chr15:75316003-75316012 chr15:75316012-75316023 chr15:75316006-75316015
27	CREB1	chr15:75315668-75316155	ECC-1	luminal epithelium:	n/a	n/a
28	HEY1	chr15:75315598-75316288	HepG2	liver:	n/a	n/a
29	POLR2A	chr15:75315683-75316346	ProgFib	skin:	n/a	n/a
30	YY1	chr15:75315665-75316194	ECC-1	luminal epithelium:	n/a	chr15:75316003-75316012 chr15:75316012-75316023 chr15:75316006-75316015
31	POLR2A	chr15:75315777-75316784	GM12878	blood:	n/a	n/a
32	ZBTB33	chr15:75315626-75316206	K562	blood:	n/a	chr15:75315878-75315893 chr15:75315923-75315938
33	TCF12	chr15:75315666-75316252	GM12878	blood:	n/a	n/a
34	POLR2A	chr15:75315761-75316655	Hela-S3	cervix:	n/a	n/a
35	ZNF384	chr15:75315377-75316068	GM12878	blood:	n/a	n/a
36	YY1	chr15:75315671-75316207	A549	lung:	n/a	chr15:75316003-75316012 chr15:75316012-75316023 chr15:75316006-75316015
37	POLR2A	chr15:75315619-75316860	PFSK-1	brain:	n/a	n/a
38	ELF1	chr15:75315611-75316149	K562	blood:	n/a	chr15:75316003-75316012
39	BHLHE40	chr15:75315706-75316176	HepG2	liver:	n/a	n/a
40	POLR2A	chr15:75315683-75317005	GM12892	blood:	n/a	n/a
41	MAX	chr15:75315725-75316062	HepG2	liver:	n/a	chr15:75315975-75315985
42	ETS1	chr15:75315643-75316206	GM12878	blood:	n/a	chr15:75315834-75315847 chr15:75315804-75315817 chr15:75315928-75315937 chr15:75316014-75316027 chr15:75315833-75315846 chr15:75315805-75315818 chr15:75315809-75315816
43	GATA1	chr15:75314966-75316097	PBDE	blood:	n/a	n/a
44	FOS	chr15:75315711-75316005	MCF10A-Er-Src	breast:	n/a	chr15:75315782-75315796
45	ZMIZ1	chr15:75315398-75316381	K562	blood:	n/a	n/a
46	ZBTB7A	chr15:75315602-75316329	K562	blood:	n/a	n/a
47	YY1	chr15:75315624-75316246	GM12878	blood:	n/a	chr15:75316003-75316012 chr15:75316012-75316023 chr15:75316006-75316015
48	POLR2A	chr15:75315623-75316825	Hela-S3	cervix:	n/a	n/a
49	MXI1	chr15:75315737-75316761	GM12878	blood:	n/a	n/a
50	POLR2A	chr15:75315646-75316272	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:75315747-75315797	HIPEpiC	eye:	n/a
2	chr15:75315747-75315797	HNPCEpiC	eye:	n/a
3	chr15:75315747-75315797	HEEpiC	esophagus:	n/a
4	chr15:75315747-75315797	GM12891	blood:	n/a
5	chr15:75315747-75315797	AG04450	lung:	fetal
6	chr15:75315747-75315797	IMR90	lung:	fetal
7	chr15:75315747-75315797	HCM	heart:	n/a
8	chr15:75315747-75315797	CMK	blood:	n/a
9	chr15:75315747-75315797	ovcar-3	ovarian:	n/a
10	chr15:75315747-75315797	Caco-2	colon:	n/a
11	chr15:75315747-75315797	NT2-D1	testis:	n/a
12	chr15:75315747-75315797	HEK293	kidney:	embryo
13	chr15:75315747-75315797	PFSK-1	brain:	n/a
14	chr15:75315747-75315797	ProgFib	skin:	n/a
15	chr15:75315747-75315797	SKMC	muscle:	n/a
16	chr15:75315747-75315797	BJ	skin:	n/a
17	chr15:75315747-75315797	BE2_C	brain:	n/a
18	chr15:75315747-75315797	LNCaP	prostate:	n/a
19	chr15:75315747-75315797	GM19239	blood:	n/a
20	chr15:75315747-75315797	HMEC	breast:	n/a
21	chr15:75315747-75315797	GM12892	blood:	n/a
22	chr15:75315747-75315797	AG10803	skin:	n/a
23	chr15:75315747-75315797	A549	lung:	n/a
24	chr15:75315747-75315797	MCF-7	breast:	n/a
25	chr15:75315747-75315797	Jurkat	blood:	n/a
26	chr15:75315747-75315797	K562	blood:	n/a
27	chr15:75315747-75315797	HUVEC	blood vessel:	n/a
28	chr15:75315747-75315797	HPAEpiC	pulmonary alveolar:	n/a
29	chr15:75315747-75315797	SK-N-SH_RA	brain:	n/a
30	chr15:75315747-75315797	NH-A	brain:	n/a
31	chr15:75315747-75315797	HCPEpiC	choroid plexus:	n/a
32	chr15:75315747-75315797	GM06990	blood:	n/a
33	chr15:75315747-75315797	NHDF-neo	bronchial:	n/a
34	chr15:75315747-75315797	ECC-1	luminal epithelium:	n/a
35	chr15:75315747-75315797	SAEC	small airway:	n/a
36	chr15:75315747-75315797	T-47D	breast:	n/a
37	chr15:75315747-75315797	PrEC	prostate:	n/a
38	chr15:75315747-75315797	HRE	kidney:	n/a
39	chr15:75315747-75315797	AG04449	skin:	fetal
40	chr15:75315747-75315797	PANC-1	pancreas:	n/a
41	chr15:75315747-75315797	NB4	blood:	n/a
42	chr15:75315747-75315797	HAEpiC	amniotic membrane:	n/a
43	chr15:75315747-75315797	AG09319	gingival:	n/a
44	chr15:75315747-75315797	HL-60	blood:	n/a
45	chr15:75315747-75315797	SK-N-MC	brain:	n/a
46	chr15:75315747-75315797	Hepatocyte	liver:	n/a
47	chr15:75315747-75315797	SK-N-SH	brain:	n/a
48	chr15:75315747-75315797	H1-hESC	embryonic stem cell:	embryo
49	chr15:75315747-75315797	RPTEC	kidney:	n/a
50	chr15:75315747-75315797	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:75315116..75318130-chr15:75502238..75505511,3	K562	blood:
2	chr15:75314427..75332274-chr15:75491598..75502885,56	MCF-7	breast:
3	chr15:75314438..75320960-chr15:75334023..75339188,6	K562	blood:
4	chr15:75314704..75323577-chr15:75491522..75500562,29	MCF-7	breast:
5	chr15:75300826..75305111-chr15:75313603..75318752,6	MCF-7	breast:
6	chr15:75163895..75166026-chr15:75315159..75317542,2	MCF-7	breast:
7	chr15:75247469..75252493-chr15:75314645..75318771,7	MCF-7	breast:
8	chr15:75313706..75315834-chr15:75659150..75661879,2	K562	blood:
9	chr15:75315711..75316297-chr9:131940036..131940688,2	Hela-S3	cervix:
10	chr15:75287417..75289225-chr15:75314885..75317439,2	MCF-7	breast:
11	chr15:75314737..75326433-chr15:75490770..75500610,30	K562	blood:
12	chr15:75302980..75304655-chr15:75315027..75317604,2	MCF-7	breast:
13	chr15:75286466..75289268-chr15:75313854..75316191,2	MCF-7	breast:
14	chr15:75246752..75249656-chr15:75313121..75316891,3	K562	blood:
15	chr15:75312886..75327225-chr15:75491522..75500922,36	K562	blood:
16	chr15:75287456..75290010-chr15:75314463..75316098,2	K562	blood:
17	chr15:75315622..75316343-chrX:53710851..53711547,2	Hela-S3	cervix:

Variant related genes	Relation type
PPCDC	TF binding region
PPCDC	CpG island
ENSG00000140497	Chromatin interaction
ENSG00000261779	Chromatin interaction
ENSG00000178718	Chromatin interaction
ENSG00000167173	Chromatin interaction
ENSG00000138621	Chromatin interaction
ENSG00000086758	Chromatin interaction
ENSG00000198794	Chromatin interaction
ENSG00000140400	Chromatin interaction
ENSG00000260274	Chromatin interaction
ENSG00000188483	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs12185077	0.87[EUR][1000 genomes]
rs12185078	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12185102	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12324912	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12591119	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12593542	0.85[LWK][hapmap]
rs12898259	0.87[AFR][1000 genomes]
rs12901243	0.87[AFR][1000 genomes]
rs12903201	0.87[AFR][1000 genomes]
rs12910644	0.84[CEU][hapmap];0.91[JPT][hapmap];0.87[EUR][1000 genomes]
rs12911421	0.95[TSI][hapmap];0.84[EUR][1000 genomes]
rs12917120	0.89[LWK][hapmap];0.90[YRI][hapmap];0.81[AFR][1000 genomes]
rs13056	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.92[MEX][hapmap];0.95[MKK][hapmap];0.97[TSI][hapmap];0.89[YRI][hapmap];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1867146	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1867150	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2083731	0.87[AFR][1000 genomes]
rs2120019	1.00[ASW][hapmap];0.92[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];0.95[TSI][hapmap];0.90[YRI][hapmap];0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2120020	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2289582	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2304899	0.83[YRI][hapmap]
rs2415253	0.87[AFR][1000 genomes]
rs2415254	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2415255	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34237279	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34655806	0.87[AFR][1000 genomes]
rs34713999	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34835684	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34913788	0.87[AFR][1000 genomes]
rs35577967	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35736167	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35911108	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3812944	0.83[YRI][hapmap]
rs3850093	1.00[CEU][hapmap];0.95[CHB][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs5020842	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[AFR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59094290	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs60425110	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6495135	0.83[ASW][hapmap];0.91[LWK][hapmap]
rs6495147	0.85[AFR][1000 genomes]
rs67324798	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs67544533	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7162900	0.85[AFR][1000 genomes]
rs7163390	0.89[LWK][hapmap]
rs7163636	0.83[YRI][hapmap]
rs7167285	0.84[AFR][1000 genomes]
rs7168680	0.85[AFR][1000 genomes]
rs7173833	0.87[AFR][1000 genomes]
rs7174129	0.83[ASW][hapmap];0.91[LWK][hapmap]
rs7175720	0.92[CEU][hapmap];0.85[GIH][hapmap];0.91[JPT][hapmap];0.83[LWK][hapmap];0.85[MEX][hapmap];0.90[TSI][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7342591	0.82[ASW][hapmap];0.91[LWK][hapmap]
rs7342601	0.83[ASW][hapmap];0.89[LWK][hapmap]
rs8028632	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.90[YRI][hapmap];0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8030089	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8033837	0.92[CEU][hapmap];0.91[JPT][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8033925	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8036197	0.87[AFR][1000 genomes]
rs8036573	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs8039755	0.83[YRI][hapmap]
rs8040169	0.87[AFR][1000 genomes]
rs8042409	0.92[CEU][hapmap];0.91[JPT][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8042558	0.83[ASW][hapmap];0.90[CHD][hapmap];0.87[JPT][hapmap];0.87[LWK][hapmap];0.86[MKK][hapmap];0.90[TSI][hapmap];0.81[ASN][1000 genomes]
rs9672995	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv569993	chr15:75242155-75483752	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
2	nsv542435	chr15:75271788-75321117	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv527237	chr15:75305040-75321262	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2304903	GLCE	cis	cerebellum	SCAN
rs2304903	CYP1A1	cis	cerebellum	SCAN
rs2304903	ULK3	cis	parietal	SCAN

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75289000-75315800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:75290000-75316000	Weak transcription	Small Intestine	intestine
3	chr15:75293200-75315800	Weak transcription	Duodenum Mucosa	Duodenum
4	chr15:75304000-75315800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr15:75304000-75316000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr15:75305000-75315800	Weak transcription	Right Ventricle	heart
7	chr15:75306200-75316000	Weak transcription	Fetal Brain Male	brain
8	chr15:75307800-75315800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr15:75308200-75315800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr15:75309000-75315800	Weak transcription	Placenta	Placenta
11	chr15:75310400-75315800	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr15:75311200-75315800	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr15:75311200-75315800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr15:75311400-75315800	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr15:75311400-75315800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr15:75311400-75315800	Weak transcription	Fetal Intestine Large	intestine
17	chr15:75312600-75315800	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr15:75312600-75315800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr15:75312600-75315800	Weak transcription	Gastric	stomach
20	chr15:75312600-75315800	Weak transcription	Pancreas	Pancrea
21	chr15:75312800-75315800	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr15:75312800-75315800	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr15:75312800-75315800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr15:75313400-75315800	Weak transcription	Colonic Mucosa	Colon
25	chr15:75313600-75315800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr15:75313800-75315800	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr15:75313800-75315800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr15:75314000-75315800	Weak transcription	Brain Germinal Matrix	brain
29	chr15:75314200-75315800	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr15:75314600-75315800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr15:75314800-75315800	Enhancers	Fetal Thymus	thymus
32	chr15:75315000-75315800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr15:75315200-75315800	Enhancers	Brain Substantia Nigra	brain
34	chr15:75315200-75315800	Enhancers	Fetal Muscle Leg	muscle
35	chr15:75315400-75315800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr15:75315400-75315800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr15:75315400-75315800	Enhancers	Primary T cells fromperipheralblood	blood
38	chr15:75315400-75315800	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr15:75315400-75315800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr15:75315400-75315800	Enhancers	Fetal Kidney	kidney
41	chr15:75315400-75315800	Flanking Active TSS	HepG2	liver
42	chr15:75315400-75315800	Enhancers	HUVEC	blood vessel
43	chr15:75315400-75316000	Enhancers	Fetal Heart	heart
44	chr15:75315600-75315800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr15:75315600-75315800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr15:75315600-75315800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr15:75315600-75315800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
48	chr15:75315600-75315800	Enhancers	Primary T cells from cord blood	blood
49	chr15:75315600-75315800	Enhancers	Primary hematopoietic stem cells	blood
50	chr15:75315600-75315800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links