Variant report

Variant	rs9267488
Chromosome Location	chr6:31514247-31514248
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	CTCF	chr6:31514204-31515545	A549	lung:	n/a	n/a
2	MAX	chr6:31514244-31514724	H1-hESC	embryonic stem cell:	n/a	chr6:31514653-31514663
3	TCF12	chr6:31514200-31514687	H1-hESC	embryonic stem cell:	n/a	n/a
4	SIN3A	chr6:31513957-31515569	H1-hESC	embryonic stem cell:	n/a	n/a
5	PBX3	chr6:31514246-31514807	SK-N-SH	brain:	n/a	n/a
6	POLR2A	chr6:31514171-31516364	HUVEC	blood vessel:	n/a	n/a
7	ATF2	chr6:31514162-31515523	H1-hESC	embryonic stem cell:	n/a	n/a
8	SP1	chr6:31514116-31515620	HCT-116	colon:	n/a	chr6:31514526-31514537 chr6:31515171-31515185 chr6:31514846-31514858 chr6:31514202-31514211 chr6:31514840-31514852 chr6:31514848-31514857 chr6:31514842-31514851 chr6:31515227-31515234 chr6:31514565-31514572 chr6:31514841-31514855 chr6:31514201-31514211 chr6:31514388-31514402 chr6:31515172-31515181 chr6:31515285-31515296 chr6:31515166-31515180 chr6:31514840-31514852
9	BCLAF1	chr6:31514205-31514932	GM12878	blood:	n/a	n/a
10	POLR2A	chr6:31514153-31515692	H1-neurons	neurons:	n/a	n/a
11	NR2F2	chr6:31514167-31516638	K562	blood:	n/a	n/a
12	REST	chr6:31514211-31514699	SK-N-SH	brain:	n/a	chr6:31514391-31514404
13	CREB1	chr6:31514189-31515729	GM12878	blood:	n/a	n/a
14	POLR2A	chr6:31514218-31514781	HCT-116	colon:	n/a	n/a
15	RCOR1	chr6:31513595-31516462	IMR90	lung:	n/a	n/a
16	POLR2A	chr6:31514116-31516326	SK-N-MC	brain:	n/a	n/a
17	CTCF	chr6:31514100-31514250	HVMF	connective:	n/a	n/a
18	RUNX3	chr6:31514208-31515635	GM12878	blood:	n/a	n/a
19	GABPA	chr6:31514188-31515704	A549	lung:	n/a	n/a
20	KAP1	chr6:31514155-31515391	U2OS	brain:	n/a	n/a
21	RAD21	chr6:31514194-31515024	MCF-7	breast:	n/a	n/a
22	MAX	chr6:31514183-31514804	SK-N-SH	brain:	n/a	chr6:31514653-31514663
23	MYBL2	chr6:31514231-31514911	HepG2	liver:	n/a	n/a
24	RAD21	chr6:31514202-31515643	HCT-116	colon:	n/a	n/a
25	SIN3AK20	chr6:31514143-31514780	H1-hESC	embryonic stem cell:	n/a	n/a
26	RAD21	chr6:31514246-31514759	SK-N-SH_RA	brain:	n/a	n/a
27	POLR2A	chr6:31514210-31514835	SK-N-SH	brain:	n/a	n/a
28	REST	chr6:31513683-31515927	H1-neurons	neurons:	n/a	chr6:31513993-31514011 chr6:31514391-31514404
29	ELF1	chr6:31514213-31514765	GM12878	blood:	n/a	n/a
30	TAF1	chr6:31514177-31514945	H1-neurons	neurons:	n/a	n/a
31	NFATC1	chr6:31514230-31515618	GM12878	blood:	n/a	n/a
32	SP1	chr6:31514057-31515743	HCT-116	colon:	n/a	chr6:31514526-31514537 chr6:31515171-31515185 chr6:31514846-31514858 chr6:31514202-31514211 chr6:31514840-31514852 chr6:31514848-31514857 chr6:31514842-31514851 chr6:31515227-31515234 chr6:31514565-31514572 chr6:31514841-31514855 chr6:31514201-31514211 chr6:31514388-31514402 chr6:31515172-31515181 chr6:31515285-31515296 chr6:31515166-31515180 chr6:31514840-31514852
33	YY1	chr6:31514185-31514711	HepG2	liver:	n/a	chr6:31514263-31514283
34	ZNF263	chr6:31513996-31515500	HEK293-T-REx	kidney:	n/a	chr6:31514533-31514554 chr6:31514462-31514483 chr6:31514494-31514515
35	TEAD4	chr6:31514235-31515678	K562	blood:	n/a	n/a
36	MAX	chr6:31514210-31514781	H1-hESC	embryonic stem cell:	n/a	chr6:31514653-31514663
37	SP4	chr6:31514154-31514838	H1-hESC	embryonic stem cell:	n/a	chr6:31514526-31514537
38	FOSL1	chr6:31514229-31514663	K562	blood:	n/a	n/a
39	SP1	chr6:31514197-31514804	A549	lung:	n/a	chr6:31514526-31514537 chr6:31514202-31514211 chr6:31514565-31514572 chr6:31514201-31514211 chr6:31514388-31514402
40	CREB1	chr6:31514203-31514877	H1-hESC	embryonic stem cell:	n/a	n/a
41	TAF1	chr6:31514230-31514866	H1-hESC	embryonic stem cell:	n/a	n/a
42	GABPA	chr6:31514222-31515722	MCF-7	breast:	n/a	n/a
43	FOSL1	chr6:31514220-31514673	H1-hESC	embryonic stem cell:	n/a	n/a
44	RAD21	chr6:31514237-31514863	H1-hESC	embryonic stem cell:	n/a	n/a
45	SIN3AK20	chr6:31514206-31514779	SK-N-SH	brain:	n/a	n/a
46	MAX	chr6:31514188-31514879	H1-hESC	embryonic stem cell:	n/a	chr6:31514843-31514853 chr6:31514653-31514663
47	GABPA	chr6:31514137-31515634	SK-N-SH	brain:	n/a	n/a
48	TAF1	chr6:31514244-31514671	GM12878	blood:	n/a	n/a
49	PBX3	chr6:31514226-31514750	SK-N-SH	brain:	n/a	n/a
50	ZNF143	chr6:31514225-31514807	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:31512487..31517874-chr6:31628889..31634381,12	K562	blood:
2	chr6:31464396..31467286-chr6:31513352..31515783,2	MCF-7	breast:
3	chr6:31513172..31514702-chr6:31830028..31832398,2	MCF-7	breast:
4	chr6:31461866..31464235-chr6:31513189..31515982,2	K562	blood:
5	chr6:31507451..31516055-chr6:31617949..31624791,11	MCF-7	breast:
6	chr6:31511781..31517209-chr6:31545410..31553496,14	K562	blood:
7	chr6:31513227..31514963-chr6:31602419..31605642,3	K562	blood:
8	chr6:31513206..31515445-chr6:31647940..31649568,2	MCF-7	breast:
9	chr6:31513047..31514729-chr6:31802148..31804053,2	MCF-7	breast:
10	chr6:31513724..31516419-chr6:31731123..31734011,2	K562	blood:
11	chr6:31462227..31464927-chr6:31513555..31516059,3	MCF-7	breast:
12	chr6:31460255..31464524-chr6:31513189..31516444,5	K562	blood:
13	chr6:31512960..31516876-chr6:31549415..31551752,3	MCF-7	breast:
14	chr6:31512174..31516924-chr6:31632110..31634699,4	MCF-7	breast:
15	chr6:31512553..31516955-chr6:31618753..31622292,7	K562	blood:
16	chr6:31511829..31516829-chr6:31586761..31590434,8	MCF-7	breast:
17	chr6:31513113..31516557-chr6:31559255..31561759,3	K562	blood:
18	chr6:31513116..31516827-chr6:31558104..31561639,4	K562	blood:
19	chr6:31513053..31519210-chr6:31585987..31595406,29	K562	blood:
20	chr6:31513771..31519008-chr6:31582734..31585702,4	K562	blood:
21	chr6:31465192..31467253-chr6:31513874..31515853,2	K562	blood:
22	chr6:31513726..31516111-chr6:31705969..31708009,2	MCF-7	breast:
23	chr6:31507406..31516955-chr6:31615847..31623354,26	K562	blood:
24	chr6:31513237..31516038-chr6:31696007..31697508,2	K562	blood:
25	chr6:31513245..31516542-chr6:31782394..31785632,3	MCF-7	breast:
26	chr6:31514014..31516004-chr6:31637492..31640233,2	MCF-7	breast:
27	chr6:31512646..31517552-chr6:31586243..31590655,20	K562	blood:
28	chr6:31513697..31516891-chr6:31590663..31594798,6	K562	blood:
29	chr6:31513816..31516540-chr6:31705988..31708603,3	K562	blood:
30	chr6:31513842..31516738-chr6:31801353..31804200,3	K562	blood:
31	chr6:31512487..31516692-chr6:31630820..31634965,11	K562	blood:
32	chr6:31514041..31516822-chr6:31607895..31609599,2	K562	blood:
33	chr6:31513234..31515924-chr6:31582326..31585070,2	K562	blood:

Variant related genes	Relation type
DDX39B	TF binding region
NFKBIL1	TF binding region
ENSG00000240053	Chromatin interaction
ENSG00000204475	Chromatin interaction
ENSG00000200816	Chromatin interaction
ENSG00000228727	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000255152	Chromatin interaction
ENSG00000227507	Chromatin interaction
ENSG00000213722	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000201207	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000201680	Chromatin interaction
ENSG00000204410	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000204516	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000204428	Chromatin interaction
ENSG00000204469	Chromatin interaction
ENSG00000204472	Chromatin interaction
ENSG00000235663	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000204435	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10214756	0.92[ASN][1000 genomes]
rs1055384	1.00[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs12181589	0.89[ASN][1000 genomes]
rs1800628	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1800629	0.88[AFR][1000 genomes]
rs2516482	0.91[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs2734583	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3093975	1.00[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs3093988	1.00[AFR][1000 genomes]
rs3094005	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3095233	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3130063	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3130612	0.90[EUR][1000 genomes]
rs3130616	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3130631	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3130923	0.87[EUR][1000 genomes]
rs9267445	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9469020	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015372	chr6:30704734-31582152	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
2	nsv538173	chr6:30704734-31582152	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
3	esv2759414	chr6:31028290-31542308	Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	151 gene(s)	inside rSNPs	diseases
4	nsv601609	chr6:31280101-31799786	Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
5	nsv601610	chr6:31280101-31960770	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	370 gene(s)	inside rSNPs	diseases
6	nsv601628	chr6:31280327-31990098	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
7	nsv601629	chr6:31280327-31996185	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
8	nsv601630	chr6:31280327-32011317	Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS 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	378 gene(s)	inside rSNPs	diseases
9	nsv601631	chr6:31280327-32017540	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
10	nsv1023939	chr6:31325961-32026747	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
11	nsv538188	chr6:31325961-32026747	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
12	nsv1018463	chr6:31337336-31525275	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	104 gene(s)	inside rSNPs	diseases
13	nsv538189	chr6:31337336-31525275	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	104 gene(s)	inside rSNPs	diseases
14	nsv432868	chr6:31338844-31721033	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	250 gene(s)	inside rSNPs	diseases
15	esv2757162	chr6:31353329-31542308	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	99 gene(s)	inside rSNPs	diseases
16	nsv1021747	chr6:31386219-31907266	Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	330 gene(s)	inside rSNPs	diseases
17	nsv432877	chr6:31412961-31528690	Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	88 gene(s)	inside rSNPs	diseases
18	nsv830627	chr6:31496214-31659950	Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
19	nsv470809	chr6:31496915-31544189	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	76 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31510600-31514600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:31510600-31514600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr6:31510600-31515800	Weak transcription	Gastric	stomach
4	chr6:31510800-31514400	Weak transcription	Right Atrium	heart
5	chr6:31510800-31514600	Weak transcription	Small Intestine	intestine
6	chr6:31510800-31515400	Weak transcription	Lung	lung
7	chr6:31511000-31514400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr6:31511000-31514400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr6:31511000-31514400	Weak transcription	Spleen	Spleen
10	chr6:31511000-31514600	Weak transcription	Right Ventricle	heart
11	chr6:31511200-31514400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr6:31511200-31514400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr6:31511200-31514400	Weak transcription	HUVEC	blood vessel
14	chr6:31511200-31514600	Weak transcription	Pancreas	Pancrea
15	chr6:31511600-31514600	Weak transcription	Psoas Muscle	Psoas
16	chr6:31513200-31514800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr6:31513200-31515800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:31513400-31514400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr6:31513400-31514600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr6:31513400-31515000	Flanking Active TSS	Brain Germinal Matrix	brain
21	chr6:31513400-31515800	Active TSS	Brain Angular Gyrus	brain
22	chr6:31513600-31514600	Flanking Active TSS	Brain Anterior Caudate	brain
23	chr6:31513600-31514600	Flanking Active TSS	Brain Substantia Nigra	brain
24	chr6:31513600-31515800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr6:31513600-31515800	Active TSS	NHDF-Ad	bronchial
26	chr6:31513600-31516000	Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr6:31513600-31516000	Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr6:31513600-31516200	Active TSS	HUES64 Cell Line	embryonic stem cell
29	chr6:31513800-31514400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr6:31513800-31514400	Flanking Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr6:31513800-31514400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
32	chr6:31513800-31514400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
33	chr6:31513800-31514400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr6:31513800-31514400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr6:31513800-31514400	Enhancers	Duodenum Smooth Muscle	Duodenum
36	chr6:31513800-31514400	Enhancers	Fetal Heart	heart
37	chr6:31513800-31514400	Enhancers	HepG2	liver
38	chr6:31513800-31514400	Flanking Active TSS	HSMM	muscle
39	chr6:31513800-31514600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr6:31513800-31514600	Flanking Active TSS	Brain Cingulate Gyrus	brain
41	chr6:31513800-31514600	Flanking Active TSS	Fetal Muscle Trunk	muscle
42	chr6:31513800-31514600	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr6:31513800-31514600	Enhancers	NHEK	skin
44	chr6:31513800-31514800	Flanking Active TSS	Fetal Muscle Leg	muscle
45	chr6:31513800-31514800	Flanking Active TSS	Fetal Stomach	stomach
46	chr6:31513800-31515000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr6:31513800-31515000	Flanking Active TSS	Stomach Smooth Muscle	stomach
48	chr6:31513800-31515200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr6:31513800-31515200	Flanking Active TSS	Dnd41	blood
50	chr6:31513800-31515600	Active TSS	H9 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links