Variant report

Variant	rs2055129
Chromosome Location	chr5:37250393-37250394
allele	A/C
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	MAX	chr5:37248769-37250415	A549	lung:	n/a	n/a
2	POLR2A	chr5:37248791-37250420	Hela-S3	cervix:	n/a	n/a
3	STAT3	chr5:37250107-37250664	MCF10A-Er-Src	breast:	n/a	n/a
4	E2F6	chr5:37248833-37250482	H1-hESC	embryonic stem cell:	n/a	chr5:37249619-37249628 chr5:37249494-37249503
5	MXI1	chr5:37248421-37250457	SK-N-SH	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:37244319..37247437-chr5:37248031..37251100,3	MCF-7	breast:

Variant related genes	Relation type
C5orf42	TF binding region
RN7SL37P	TF binding region
ENSG00000242493	Chromatin interaction

Extended variants
information (count: 107 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs10037834	0.81[EUR][1000 genomes]
rs10043395	0.82[EUR][1000 genomes]
rs10052880	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10056009	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs10057270	1.00[CEU][hapmap];0.91[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.87[TSI][hapmap];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10068328	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10068501	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10069109	0.88[CEU][hapmap];0.95[GIH][hapmap];0.86[MEX][hapmap];0.94[TSI][hapmap];0.88[EUR][1000 genomes]
rs10072064	1.00[CEU][hapmap];0.95[GIH][hapmap];0.93[MEX][hapmap];0.94[TSI][hapmap];0.88[EUR][1000 genomes]
rs10072288	1.00[CEU][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes]
rs10076911	1.00[CEU][hapmap];0.91[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.94[TSI][hapmap];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10805625	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs10941320	0.87[EUR][1000 genomes]
rs10941322	0.83[ASN][1000 genomes]
rs10941323	0.82[AMR][1000 genomes]
rs10941324	0.90[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10941325	0.82[AMR][1000 genomes]
rs10941327	0.85[LWK][hapmap];0.86[MEX][hapmap]
rs10941329	0.81[MEX][hapmap]
rs11744730	0.82[AMR][1000 genomes]
rs11750291	0.84[AMR][1000 genomes]
rs11958752	1.00[CEU][hapmap];0.91[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.94[TSI][hapmap];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12108953	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12110010	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12110069	0.88[EUR][1000 genomes]
rs12186733	1.00[CEU][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs12189377	0.86[ASN][1000 genomes]
rs12515518	0.89[ASW][hapmap];1.00[CEU][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];0.94[TSI][hapmap];0.91[YRI][hapmap];0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12515522	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12515577	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12516541	0.82[AMR][1000 genomes]
rs12518867	0.82[CEU][hapmap];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12522481	0.82[AMR][1000 genomes]
rs12523044	0.90[ASN][1000 genomes]
rs16903526	1.00[CEU][hapmap];0.91[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.94[TSI][hapmap];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16903578	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.94[TSI][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16903587	0.82[AMR][1000 genomes]
rs16903601	0.88[LWK][hapmap];0.86[MEX][hapmap]
rs17511925	0.90[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2081109	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2270559	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2272601	0.88[LWK][hapmap];0.86[MEX][hapmap];0.82[AMR][1000 genomes]
rs2272602	0.82[AMR][1000 genomes]
rs2365910	1.00[CEU][hapmap];0.91[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.94[TSI][hapmap];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2365912	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2366275	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2886505	0.83[EUR][1000 genomes]
rs301861	0.88[EUR][1000 genomes]
rs301862	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs301864	0.85[EUR][1000 genomes]
rs301866	0.88[EUR][1000 genomes]
rs301868	0.88[EUR][1000 genomes]
rs301870	1.00[CEU][hapmap];0.95[GIH][hapmap];0.93[MEX][hapmap];0.94[TSI][hapmap];0.88[EUR][1000 genomes]
rs301871	0.88[EUR][1000 genomes]
rs301876	0.88[EUR][1000 genomes]
rs301877	0.88[EUR][1000 genomes]
rs301890	1.00[CEU][hapmap];0.84[CHD][hapmap];1.00[JPT][hapmap]
rs301891	1.00[CEU][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.94[TSI][hapmap];0.88[EUR][1000 genomes]
rs301892	1.00[CEU][hapmap]
rs301893	1.00[CEU][hapmap]
rs301895	1.00[CEU][hapmap]
rs301904	1.00[CEU][hapmap]
rs301907	0.88[EUR][1000 genomes]
rs301910	0.88[EUR][1000 genomes]
rs301911	0.88[EUR][1000 genomes]
rs301914	0.85[EUR][1000 genomes]
rs301915	0.85[EUR][1000 genomes]
rs301916	0.85[EUR][1000 genomes]
rs59278603	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59324297	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs59842820	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6859227	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6897283	1.00[CEU][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.94[TSI][hapmap];0.88[EUR][1000 genomes]
rs73068411	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73750950	0.91[EUR][1000 genomes]
rs7712984	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7724454	1.00[CEU][hapmap];0.95[GIH][hapmap];0.93[MEX][hapmap];0.94[TSI][hapmap];0.88[EUR][1000 genomes]
rs9292649	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9687825	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.94[TSI][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525478	chr5:36804225-37349895	Strong transcription Transcr. at gene 5' and 3' Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	esv1793961	chr5:36866835-37361728	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
3	nsv530225	chr5:36886635-37331912	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	nsv1024051	chr5:36899712-37303001	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv537725	chr5:36899712-37303001	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
6	nsv530226	chr5:36906377-37606367	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
7	nsv534064	chr5:37054962-37586210	Active TSS Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
8	nsv881511	chr5:37088627-37552852	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
9	nsv597823	chr5:37111565-37430365	Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
10	nsv1026554	chr5:37112133-37734859	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
11	nsv537726	chr5:37112133-37734859	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
12	nsv1025988	chr5:37115142-37586211	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
13	nsv537727	chr5:37115142-37586211	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
14	nsv830265	chr5:37152221-37312233	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
15	nsv530227	chr5:37157106-37571999	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
16	nsv880406	chr5:37173930-37345270	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
17	nsv880839	chr5:37173930-37465126	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
18	nsv948741	chr5:37179341-37582164	Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
19	nsv949716	chr5:37179341-37967352	Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
20	nsv597824	chr5:37206621-37409579	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
21	nsv597825	chr5:37206621-37430365	Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
22	esv3358042	chr5:37232244-37251247	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
23	nsv881512	chr5:37239240-37364693	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
24	nsv880817	chr5:37239240-37465126	Weak transcription Bivalent Enhancer Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
25	nsv881492	chr5:37239240-37543121	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
26	nsv880444	chr5:37239240-37556926	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
27	nsv1015983	chr5:37240827-37666601	Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
28	esv3341332	chr5:37248220-37250768	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2055129	C5orf42	cis	cerebellum	SCAN
rs2055129	C6	cis	cerebellum	SCAN

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37247400-37250400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr5:37248600-37250400	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr5:37249600-37250400	Flanking Active TSS	Dnd41	blood
4	chr5:37249800-37250400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr5:37249800-37250400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr5:37249800-37250400	Flanking Active TSS	Brain Hippocampus Middle	brain
7	chr5:37249800-37250400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
8	chr5:37249800-37250400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
9	chr5:37249800-37250400	Enhancers	Spleen	Spleen
10	chr5:37249800-37250400	Flanking Active TSS	A549	lung
11	chr5:37249800-37250400	Flanking Active TSS	Hela-S3	cervix
12	chr5:37249800-37250400	Flanking Active TSS	HSMM	muscle
13	chr5:37250000-37250400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
14	chr5:37250000-37250400	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
15	chr5:37250000-37250400	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr5:37250000-37250400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr5:37250000-37250400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
18	chr5:37250000-37250400	Flanking Active TSS	Brain Cingulate Gyrus	brain
19	chr5:37250000-37250400	Enhancers	Esophagus	oesophagus
20	chr5:37250000-37250400	Flanking Active TSS	Fetal Intestine Large	intestine
21	chr5:37250000-37250400	Enhancers	Gastric	stomach
22	chr5:37250000-37250400	Enhancers	Lung	lung
23	chr5:37250000-37250600	Enhancers	Primary T helper cells fromperipheralblood	blood
24	chr5:37250000-37251600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr5:37250200-37250400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr5:37250200-37250400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr5:37250200-37250400	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr5:37250200-37250400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
29	chr5:37250200-37250400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr5:37250200-37250400	Enhancers	Primary hematopoietic stem cells	blood
31	chr5:37250200-37250400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr5:37250200-37250400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr5:37250200-37250400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr5:37250200-37250400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr5:37250200-37250400	Enhancers	Adipose Nuclei	Adipose
36	chr5:37250200-37250400	Flanking Active TSS	Brain Angular Gyrus	brain
37	chr5:37250200-37250400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
38	chr5:37250200-37250400	Enhancers	Brain Substantia Nigra	brain
39	chr5:37250200-37250400	Enhancers	Colon Smooth Muscle	Colon
40	chr5:37250200-37250400	Enhancers	Duodenum Smooth Muscle	Duodenum
41	chr5:37250200-37250400	Enhancers	Fetal Heart	heart
42	chr5:37250200-37250400	Active TSS	Fetal Muscle Trunk	muscle
43	chr5:37250200-37250400	Enhancers	Fetal Thymus	thymus
44	chr5:37250200-37250400	Enhancers	Left Ventricle	heart
45	chr5:37250200-37250400	Active TSS	Stomach Smooth Muscle	stomach
46	chr5:37250200-37250400	Enhancers	GM12878-XiMat	blood
47	chr5:37250200-37250400	Enhancers	NH-A	brain
48	chr5:37250200-37250400	Enhancers	NHLF	lung
49	chr5:37250200-37250600	Enhancers	Fetal Brain Female	brain
50	chr5:37250200-37250600	Active TSS	Skeletal Muscle Male	skeletal muscle

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