Variant report

Variant	rs2242577
Chromosome Location	chr1:155224301-155224302
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:27)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:27 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr1:155224160-155224410	GM12870	blood:	n/a	chr1:155224342-155224360
2	CTCF	chr1:155224260-155224410	HRPEpiC	eye:	n/a	chr1:155224342-155224360
3	MAX	chr1:155224161-155224551	K562	blood:	n/a	n/a
4	MAZ	chr1:155224131-155225987	IMR90	lung:	n/a	n/a
5	CTCF	chr1:155224240-155224390	HBMEC	blood vessel:	n/a	chr1:155224342-155224360
6	ZNF263	chr1:155223133-155226440	HEK293-T-REx	kidney:	n/a	chr1:155225286-155225295 chr1:155225617-155225626
7	CTCF	chr1:155224220-155224370	AG04449	skin:	n/a	chr1:155224342-155224360
8	SIN3AK20	chr1:155224079-155224877	PANC-1	pancreas:	n/a	n/a
9	POLR2A	chr1:155223847-155226981	SK-N-MC	brain:	n/a	n/a
10	RUNX3	chr1:155224100-155224363	GM12878	blood:	n/a	n/a
11	CTCF	chr1:155224280-155224430	HAc	cerebellar:	n/a	chr1:155224342-155224360
12	POLR2A	chr1:155223686-155224717	PFSK-1	brain:	n/a	n/a
13	MAX	chr1:155224082-155225765	A549	lung:	n/a	n/a
14	POLR2A	chr1:155224133-155226107	HUVEC	blood vessel:	n/a	n/a
15	CTCF	chr1:155224260-155224410	AG09319	gingival:	n/a	chr1:155224342-155224360
16	CTCF	chr1:155224180-155224330	HMEC	breast:	n/a	n/a
17	MAX	chr1:155224153-155225515	MCF-7	breast:	n/a	n/a
18	MXI1	chr1:155223540-155226345	IMR90	lung:	n/a	n/a
19	CTCF	chr1:155224280-155224430	BJ	skin:	n/a	chr1:155224342-155224360
20	MAX	chr1:155224252-155224380	K562	blood:	n/a	n/a
21	CTBP2	chr1:155224147-155225601	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr1:155224227-155224788	HepG2	liver:	n/a	n/a
23	MTA3	chr1:155224020-155225608	GM12878	blood:	n/a	n/a
24	CTCF	chr1:155224300-155224450	HVMF	connective:	n/a	chr1:155224342-155224360
25	MXI1	chr1:155222997-155226068	SK-N-SH	brain:	n/a	n/a
26	CTCF	chr1:155224280-155224430	HCPEpiC	choroid plexus:	n/a	chr1:155224342-155224360
27	SIN3AK20	chr1:155224260-155224694	SK-N-SH	brain:	n/a	n/a

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:155223569..155226696-chr1:155275954..155279861,6	K562	blood:
2	chr1:155223569..155227620-chr1:155275954..155279861,5	K562	blood:
3	chr1:149907697..149909592-chr1:155223103..155225429,2	MCF-7	breast:
4	chr1:155223794..155226979-chr1:155292101..155295505,5	K562	blood:
5	chr1:155194687..155197665-chr1:155223228..155225374,3	MCF-7	breast:
6	chr1:155210404..155213133-chr1:155222950..155225276,2	MCF-7	breast:
7	chr1:155223788..155226914-chr1:155293518..155296850,4	K562	blood:
8	chr1:155221948..155224777-chr1:155277014..155278574,2	MCF-7	breast:
9	chr1:155021843..155023415-chr1:155222599..155225501,2	MCF-7	breast:
10	chr1:155223299..155226083-chr1:155288003..155289831,2	MCF-7	breast:
11	chr1:155218456..155235751-chr1:155288837..155299195,44	MCF-7	breast:
12	chr1:155162819..155165123-chr1:155223142..155225278,3	K562	blood:
13	chr1:155213237..155217995-chr1:155221685..155226391,8	MCF-7	breast:

No data

Variant related genes	Relation type
FAM189B	TF binding region
ENSG00000225855	Chromatin interaction
ENSG00000143537	Chromatin interaction
ENSG00000014914	Chromatin interaction
ENSG00000160766	Chromatin interaction
ENSG00000177628	Chromatin interaction
ENSG00000160752	Chromatin interaction
ENSG00000160753	Chromatin interaction
ENSG00000271748	Chromatin interaction

Extended variants
information (count: 118 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:101)

rs_ID	r²[population]
rs10128085	0.81[EUR][1000 genomes]
rs1045253	0.88[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1046188	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1052176	0.93[ASN][1000 genomes]
rs1052177	0.93[ASN][1000 genomes]
rs1076556	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1078699	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10796940	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10796943	0.82[CHB][hapmap]
rs10908459	0.91[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10908463	0.83[CHB][hapmap];0.82[CHD][hapmap]
rs10908465	0.83[CHB][hapmap]
rs11264337	0.86[YRI][hapmap]
rs11264338	0.86[YRI][hapmap]
rs11264339	0.86[YRI][hapmap]
rs11264343	0.88[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11264345	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs11264346	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11264347	0.90[EUR][1000 genomes]
rs11264348	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11264349	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11264351	0.88[ASN][1000 genomes]
rs11264352	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11264353	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11264354	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11264355	0.86[ASN][1000 genomes]
rs11264359	0.89[CHB][hapmap];0.85[CHD][hapmap]
rs11264361	0.83[CHB][hapmap];0.82[CHD][hapmap]
rs11264367	0.83[CHB][hapmap]
rs11264369	0.83[CHB][hapmap]
rs11264371	0.83[CHB][hapmap]
rs11264372	0.83[CHB][hapmap]
rs11264375	0.83[CHB][hapmap]
rs1142287	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11577338	0.95[ASN][1000 genomes]
rs12026638	0.89[CHB][hapmap]
rs12034326	0.87[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs12041534	0.83[CHB][hapmap]
rs12042020	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12044063	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12049375	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12067675	0.87[ASN][1000 genomes]
rs12239114	0.83[CHB][hapmap]
rs12407919	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12563994	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12723761	0.87[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12724449	0.80[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12730000	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12732972	0.83[ASN][1000 genomes]
rs12748155	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12749306	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1325908	0.83[CHB][hapmap]
rs1546818	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1800438	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1800442	0.88[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1807042	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2009578	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2071053	0.93[ASN][1000 genomes]
rs2072647	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2075566	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2075569	0.89[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2236863	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2236864	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2242576	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2297480	0.94[CHB][hapmap];0.89[CHD][hapmap];0.85[JPT][hapmap]
rs2361536	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2361543	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28373017	0.83[ASN][1000 genomes]
rs3020781	0.83[ASN][1000 genomes]
rs34906309	0.89[ASN][1000 genomes]
rs3754485	0.89[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3762272	0.85[ASN][1000 genomes]
rs3768566	0.89[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs3814318	0.91[ASN][1000 genomes]
rs3814319	0.91[ASN][1000 genomes]
rs4043	0.87[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4421576	0.86[YRI][hapmap]
rs4460629	0.82[YRI][hapmap]
rs4620533	0.93[ASN][1000 genomes]
rs4971079	0.89[YRI][hapmap]
rs4971085	0.86[YRI][hapmap]
rs4971088	0.86[YRI][hapmap]
rs5005770	0.83[CHB][hapmap]
rs56310840	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs56750937	0.80[ASN][1000 genomes]
rs59062514	0.85[ASN][1000 genomes]
rs59352002	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs734073	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs734074	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs741756	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7520184	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7543234	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7549276	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7554780	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7556304	0.86[YRI][hapmap]
rs762488	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs8177968	0.90[ASN][1000 genomes]
rs8847	0.93[ASN][1000 genomes]
rs932972	0.93[ASN][1000 genomes]
rs9628662	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9729564	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532579	chr1:154548165-155262692	Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	575 gene(s)	inside rSNPs	diseases
2	esv1823746	chr1:154965207-155231904	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	469 gene(s)	inside rSNPs	diseases
3	nsv831614	chr1:155094978-155275031	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	434 gene(s)	inside rSNPs	diseases
4	esv2757756	chr1:155094978-155314807	Bivalent Enhancer Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	452 gene(s)	inside rSNPs	diseases
5	esv2758971	chr1:155094978-155314807	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	452 gene(s)	inside rSNPs	diseases
6	nsv470741	chr1:155115260-155230131	Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	381 gene(s)	inside rSNPs	diseases
7	nsv872457	chr1:155135335-155310443	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	407 gene(s)	inside rSNPs	diseases
8	nsv831625	chr1:155145634-155313409	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	407 gene(s)	inside rSNPs	diseases
9	nsv529709	chr1:155154933-155757219	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	450 gene(s)	inside rSNPs	diseases
10	nsv1008748	chr1:155189148-155230610	Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
11	nsv1011773	chr1:155189148-155234821	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
12	nsv947198	chr1:155206997-155226440	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	35 gene(s)	inside rSNPs	diseases
13	esv1832331	chr1:155213136-155271366	Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
14	esv1826485	chr1:155214478-155264270	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
15	esv1824971	chr1:155215985-155260869	Genic enhancers Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
16	nsv831636	chr1:155219223-155444864	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers 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 miRNA target site	67 gene(s)	inside rSNPs	diseases
17	esv33869	chr1:155223283-155917961	Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	187 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs2242577	GBAP1	cis	Thyroid	GTEx
rs2242577	THBS3	cis	Whole Blood	GTEx
rs2242577	GBAP1	cis	Artery Tibial	GTEx
rs2242577	RIT1	Cis_1M	lymphoblastoid	RTeQTL
rs2242577	FDPS	Cis_1M	lymphoblastoid	RTeQTL
rs2242577	GBA	cis	Esophagus Mucosa	GTEx
rs2242577	RP11-263K19.4	cis	Whole Blood	GTEx

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155220600-155224600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr1:155220800-155224400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr1:155221000-155224400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr1:155223000-155224800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr1:155223200-155224400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr1:155223200-155224400	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr1:155223200-155224400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr1:155223200-155224400	Enhancers	Placenta Amnion	Placenta Amnion
9	chr1:155223200-155224600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
10	chr1:155223200-155224600	Flanking Active TSS	Hela-S3	cervix
11	chr1:155223200-155224600	Flanking Active TSS	HepG2	liver
12	chr1:155223200-155224600	Flanking Active TSS	NHLF	lung
13	chr1:155223200-155224800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr1:155223200-155224800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr1:155223200-155224800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
16	chr1:155223200-155224800	Flanking Active TSS	Dnd41	blood
17	chr1:155223200-155225000	Flanking Active TSS	Stomach Smooth Muscle	stomach
18	chr1:155223200-155226000	Active TSS	iPS-18 Cell Line	embryonic stem cell
19	chr1:155223200-155227600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr1:155223400-155224400	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr1:155223400-155224400	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr1:155223400-155224400	Flanking Active TSS	Brain Angular Gyrus	brain
23	chr1:155223400-155224400	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
24	chr1:155223400-155224400	Enhancers	Fetal Heart	heart
25	chr1:155223400-155224400	Enhancers	Fetal Thymus	thymus
26	chr1:155223400-155224400	Enhancers	Spleen	Spleen
27	chr1:155223400-155224400	Flanking Active TSS	Osteobl	bone
28	chr1:155223400-155224600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
29	chr1:155223400-155224600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr1:155223400-155224600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr1:155223400-155224600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr1:155223400-155224600	Flanking Active TSS	Brain Cingulate Gyrus	brain
33	chr1:155223400-155224600	Flanking Active TSS	Brain Germinal Matrix	brain
34	chr1:155223400-155224600	Flanking Active TSS	Brain Hippocampus Middle	brain
35	chr1:155223400-155224600	Flanking Active TSS	NH-A	brain
36	chr1:155223400-155224800	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr1:155223400-155224800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
38	chr1:155223400-155224800	Flanking Active TSS	Duodenum Mucosa	Duodenum
39	chr1:155223400-155224800	Flanking Active TSS	Fetal Brain Female	brain
40	chr1:155223400-155224800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
41	chr1:155223400-155224800	Flanking Active TSS	K562	blood
42	chr1:155223400-155225000	Flanking Active TSS	HUVEC	blood vessel
43	chr1:155223400-155226000	Flanking Active TSS	HMEC	breast
44	chr1:155223600-155224400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr1:155223600-155224400	Enhancers	Liver	Liver
46	chr1:155223600-155224400	Enhancers	Lung	lung
47	chr1:155223600-155224400	Enhancers	Small Intestine	intestine
48	chr1:155223600-155224600	Enhancers	Primary B cells from peripheral blood	blood
49	chr1:155223600-155224600	Enhancers	Primary T cells fromperipheralblood	blood
50	chr1:155223600-155224600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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