Variant report

Variant	rs6601536
Chromosome Location	chr8:10696311-10696312
allele	C/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	SMC3	chr8:10695944-10697003	SK-N-SH	brain:	n/a	chr8:10696560-10696574
2	HCFC1	chr8:10696157-10697962	Hela-S3	cervix:	n/a	n/a
3	MXI1	chr8:10696152-10697954	GM12878	blood:	n/a	n/a
4	POLR2A	chr8:10695994-10696797	HepG2	liver:	n/a	n/a
5	RAD21	chr8:10696267-10696682	MCF-7	breast:	n/a	chr8:10696556-10696575 chr8:10696558-10696570
6	IRF1	chr8:10696308-10696762	K562	blood:	n/a	n/a
7	REST	chr8:10696169-10697919	H1-neurons	neurons:	n/a	chr8:10697451-10697464
8	RAD21	chr8:10696290-10696873	ECC-1	luminal epithelium:	n/a	chr8:10696556-10696575 chr8:10696558-10696570
9	CTCF	chr8:10696150-10696915	HCT-116	colon:	n/a	chr8:10696558-10696576 chr8:10696560-10696573 chr8:10696559-10696575 chr8:10696553-10696574
10	MXI1	chr8:10696242-10697893	IMR90	lung:	n/a	n/a
11	POLR2A	chr8:10696231-10696848	PFSK-1	brain:	n/a	n/a
12	POLR2A	chr8:10696117-10696888	HepG2	liver:	n/a	n/a
13	EP300	chr8:10696299-10696558	GM12878	blood:	n/a	n/a
14	MXI1	chr8:10696164-10698606	SK-N-SH	brain:	n/a	n/a
15	POLR2A	chr8:10696084-10698426	GM12891	blood:	n/a	n/a
16	RAD21	chr8:10696286-10696835	A549	lung:	n/a	chr8:10696556-10696575 chr8:10696558-10696570
17	POLR2A	chr8:10695983-10697821	GM12878	blood:	n/a	n/a
18	POLR2A	chr8:10696268-10696716	GM12892	blood:	n/a	n/a
19	POLR2A	chr8:10696212-10698336	K562	blood:	n/a	n/a
20	USF2	chr8:10696020-10696654	GM12878	blood:	n/a	n/a
21	RAD21	chr8:10696290-10696836	H1-hESC	embryonic stem cell:	n/a	chr8:10696556-10696575 chr8:10696558-10696570
22	MYC	chr8:10696087-10697961	K562	blood:	n/a	n/a
23	POLR2A	chr8:10696270-10697725	IMR90	lung:	n/a	n/a
24	POLR2A	chr8:10696302-10697927	GM12892	blood:	n/a	n/a
25	POLR2A	chr8:10696283-10697871	K562	blood:	n/a	n/a
26	TCF12	chr8:10696183-10697785	ECC-1	luminal epithelium:	n/a	n/a
27	BHLHE40	chr8:10696305-10698013	GM12878	blood:	n/a	chr8:10697375-10697391 chr8:10697367-10697383
28	CTCF	chr8:10696264-10696953	GM12878	blood:	n/a	chr8:10696558-10696576 chr8:10696560-10696573 chr8:10696559-10696575 chr8:10696553-10696574
29	CTCF	chr8:10696012-10697813	SK-N-SH	brain:	n/a	chr8:10696558-10696576 chr8:10696560-10696573 chr8:10696559-10696575 chr8:10696553-10696574
30	RAD21	chr8:10696219-10696837	A549	lung:	n/a	chr8:10696556-10696575 chr8:10696558-10696570
31	EP300	chr8:10696262-10696671	HepG2	liver:	n/a	n/a
32	MAZ	chr8:10696236-10696710	GM12878	blood:	n/a	n/a
33	POLR2A	chr8:10696074-10696878	GM12878	blood:	n/a	n/a
34	CTCF	chr8:10696301-10696900	HCT-116	colon:	n/a	chr8:10696558-10696576 chr8:10696560-10696573 chr8:10696559-10696575 chr8:10696553-10696574
35	POLR2A	chr8:10696200-10697886	H1-hESC	embryonic stem cell:	n/a	n/a
36	RAD21	chr8:10696176-10696933	SK-N-SH	brain:	n/a	chr8:10696556-10696575 chr8:10696558-10696570
37	RAD21	chr8:10696181-10696988	HCT-116	colon:	n/a	chr8:10696556-10696575 chr8:10696558-10696570
38	POLR2A	chr8:10696269-10696850	K562	blood:	n/a	n/a
39	RAD21	chr8:10696265-10696884	HCT-116	colon:	n/a	chr8:10696556-10696575 chr8:10696558-10696570
40	PML	chr8:10696270-10697996	GM12878	blood:	n/a	n/a
41	CTCF	chr8:10695761-10698042	A549	lung:	n/a	chr8:10696558-10696576 chr8:10696560-10696573 chr8:10696559-10696575 chr8:10696553-10696574

No.	Distal block	Cell Line	Cell type
1	chr8:10683525..10686850-chr8:10694502..10697878,5	K562	blood:
2	chr8:10683547..10686608-chr8:10694341..10697878,5	K562	blood:
3	chr8:10447281..10448089-chr8:10696064..10697196,3	MCF-7	breast:
4	chr8:10674954..10678350-chr8:10693952..10697087,3	K562	blood:
5	chr8:10442817..10445019-chr8:10695179..10696964,2	MCF-7	breast:
6	chr8:10694381..10696683-chr8:10699083..10701009,2	K562	blood:
7	chr8:10694766..10696620-chr8:10707984..10711858,3	K562	blood:
8	chr8:10687156..10690707-chr8:10693616..10698468,7	K562	blood:
9	chr8:10690421..10694581-chr8:10695821..10698975,5	MCF-7	breast:
10	chr8:10405123..10407146-chr8:10694080..10697115,3	MCF-7	breast:
11	chr8:10405304..10405893-chr8:10696191..10696982,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000253695	TF binding region
ENSG00000254093	Chromatin interaction

Extended variants
information (count: 97 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs10046628	1.00[CHB][hapmap];0.93[JPT][hapmap];0.95[ASN][1000 genomes]
rs10088888	0.81[ASN][1000 genomes]
rs10089153	0.94[CHB][hapmap];0.81[ASN][1000 genomes]
rs10091386	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10093774	0.81[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.85[GIH][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs10098699	0.81[CEU][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs10099929	0.98[ASN][1000 genomes]
rs10109416	0.87[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10109550	0.87[CHB][hapmap]
rs10481451	0.81[CEU][hapmap]
rs1055329	0.83[CHD][hapmap]
rs11250077	0.81[CEU][hapmap]
rs11250081	0.98[ASN][1000 genomes]
rs11250083	1.00[CHB][hapmap];0.90[CHD][hapmap];0.88[JPT][hapmap];0.90[ASN][1000 genomes]
rs11776674	0.93[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs11776767	0.94[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs11986043	0.92[CEU][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11986845	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11986935	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11996727	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12541110	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12676417	0.81[CEU][hapmap]
rs13254059	0.89[ASN][1000 genomes]
rs13254592	0.89[ASN][1000 genomes]
rs13274017	0.90[ASN][1000 genomes]
rs1469556	1.00[CHB][hapmap];0.88[JPT][hapmap];0.89[ASN][1000 genomes]
rs1549796	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17152576	0.90[ASN][1000 genomes]
rs1991649	0.90[ASN][1000 genomes]
rs1991650	1.00[CHB][hapmap];0.90[CHD][hapmap];0.88[JPT][hapmap];0.90[ASN][1000 genomes]
rs1991651	0.81[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.87[GIH][hapmap];0.88[JPT][hapmap];0.90[ASN][1000 genomes]
rs2271355	1.00[ASW][hapmap];0.96[CEU][hapmap];0.83[CHD][hapmap];0.95[GIH][hapmap];0.94[JPT][hapmap];0.95[LWK][hapmap];0.94[MEX][hapmap];0.97[MKK][hapmap];0.89[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2271357	0.85[ASW][hapmap];0.94[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2277130	0.80[CEU][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs2278335	1.00[CHB][hapmap];0.96[CHD][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs2292370	0.94[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs2292371	0.87[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs2409649	0.93[ASN][1000 genomes]
rs2409650	0.93[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs28613656	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34653170	0.85[ASN][1000 genomes]
rs35091929	0.98[ASN][1000 genomes]
rs3808603	0.96[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.98[GIH][hapmap];0.94[JPT][hapmap];0.94[MEX][hapmap];0.84[TSI][hapmap];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3808605	0.82[ASN][1000 genomes]
rs4840519	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4841452	0.82[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6601529	0.81[CEU][hapmap]
rs6601533	0.92[ASN][1000 genomes]
rs6601534	0.96[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];0.94[JPT][hapmap];0.94[MEX][hapmap];0.82[MKK][hapmap];0.89[TSI][hapmap];0.82[YRI][hapmap];0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6601535	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs66844016	0.93[ASN][1000 genomes]
rs67211633	0.90[ASN][1000 genomes]
rs6980805	0.81[CEU][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs6982769	0.93[ASN][1000 genomes]
rs6984388	0.93[ASN][1000 genomes]
rs6987200	0.93[ASN][1000 genomes]
rs6988598	0.87[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6989160	0.81[CEU][hapmap]
rs6989846	0.87[CHB][hapmap]
rs6990055	0.94[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6990589	0.87[CHB][hapmap];0.93[CHD][hapmap]
rs6991499	0.94[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6991526	0.94[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6992366	0.94[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6993121	0.87[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs7000939	0.94[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs7001887	0.98[ASN][1000 genomes]
rs7002282	0.81[CEU][hapmap]
rs7004998	0.94[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7005531	0.81[CHB][hapmap];0.83[CHD][hapmap]
rs7010680	0.95[ASN][1000 genomes]
rs7010709	0.87[CHB][hapmap];0.86[CHD][hapmap]
rs7012206	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7013032	1.00[CHB][hapmap];0.82[JPT][hapmap];0.91[ASN][1000 genomes]
rs7814757	0.80[CEU][hapmap]
rs7818181	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];1.00[MEX][hapmap];1.00[MKK][hapmap];0.89[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7824384	0.87[CHB][hapmap]
rs7825100	0.89[ASN][1000 genomes]
rs7829089	0.94[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7829201	0.92[ASN][1000 genomes]
rs7830317	0.97[ASN][1000 genomes]
rs7830431	0.92[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.97[ASN][1000 genomes]
rs7833128	0.93[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7833945	0.80[CEU][hapmap];0.94[CHB][hapmap];0.93[JPT][hapmap];0.97[ASN][1000 genomes]
rs7840785	0.81[CHB][hapmap];0.83[CHD][hapmap]
rs7846449	0.94[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs9969626	0.80[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917085	chr8:10237508-10828204	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv1026802	chr8:10576444-10754489	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
3	nsv539469	chr8:10576444-10754489	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
4	nsv1017836	chr8:10591801-10803617	Enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
5	nsv1034988	chr8:10591801-10804243	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
6	nsv831232	chr8:10606053-10774948	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
7	nsv1019754	chr8:10617908-10700140	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
8	nsv539471	chr8:10617908-10700140	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
9	nsv1031726	chr8:10627742-10749369	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
10	nsv508497	chr8:10680621-10750255	Genic enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs6601536	AMAC1L2	cis	parietal	SCAN
rs6601536	MFHAS1	cis	cerebellum	SCAN
rs6601536	DEFB136	cis	parietal	SCAN
rs6601536	FLJ10661	cis	cerebellum	SCAN
rs6601536	CLDN23	cis	multi-tissue	Pritchard
rs6601536	DEFA6	cis	parietal	SCAN
rs6601536	C8orf5	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10686200-10696600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:10686400-10696400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:10688800-10696400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr8:10691400-10696600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr8:10691400-10696600	Weak transcription	Small Intestine	intestine
6	chr8:10691600-10696600	Weak transcription	Aorta	Aorta
7	chr8:10691800-10696600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr8:10691800-10696600	Weak transcription	Lung	lung
9	chr8:10691800-10696600	Weak transcription	Ovary	ovary
10	chr8:10692000-10696600	Weak transcription	Esophagus	oesophagus
11	chr8:10692000-10696600	Weak transcription	Gastric	stomach
12	chr8:10692000-10696600	Weak transcription	Right Ventricle	heart
13	chr8:10692000-10696600	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr8:10692000-10696800	Weak transcription	Spleen	Spleen
15	chr8:10692400-10696600	Weak transcription	Left Ventricle	heart
16	chr8:10692800-10696400	Weak transcription	Fetal Muscle Trunk	muscle
17	chr8:10694400-10696400	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr8:10695000-10696400	Weak transcription	Pancreas	Pancrea
19	chr8:10695400-10696600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr8:10695800-10696400	Flanking Active TSS	K562	blood
21	chr8:10695800-10696600	Flanking Active TSS	HMEC	breast
22	chr8:10695800-10698000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr8:10696000-10696400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:10696000-10696400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
25	chr8:10696000-10696400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr8:10696000-10696400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr8:10696000-10696400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
28	chr8:10696000-10696400	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr8:10696000-10696400	Enhancers	Primary B cells from peripheral blood	blood
30	chr8:10696000-10696400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr8:10696000-10696400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr8:10696000-10696400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr8:10696000-10696400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr8:10696000-10696400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr8:10696000-10696400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr8:10696000-10696400	Enhancers	Brain Germinal Matrix	brain
37	chr8:10696000-10696400	Enhancers	Brain Substantia Nigra	brain
38	chr8:10696000-10696400	Enhancers	Colon Smooth Muscle	Colon
39	chr8:10696000-10696400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr8:10696000-10696400	Enhancers	Fetal Stomach	stomach
41	chr8:10696000-10696400	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr8:10696000-10696400	Flanking Active TSS	A549	lung
43	chr8:10696000-10696400	Enhancers	HSMMtube	muscle
44	chr8:10696000-10696400	Flanking Active TSS	NHLF	lung
45	chr8:10696000-10696600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr8:10696000-10696600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
47	chr8:10696000-10696600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr8:10696000-10696600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr8:10696000-10696600	Flanking Active TSS	Hela-S3	cervix
50	chr8:10696000-10696600	Flanking Active TSS	HepG2	liver

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