Variant report

Variant	rs61413963
Chromosome Location	chr8:1771112-1771113
allele	C/T
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	MAFK	chr8:1771052-1771387	H1-hESC	embryonic stem cell:	n/a	chr8:1771171-1771186 chr8:1771170-1771184 chr8:1771171-1771187 chr8:1771171-1771182 chr8:1771171-1771182
2	MAFF	chr8:1771019-1771365	K562	blood:	n/a	chr8:1771169-1771187
3	MYC	chr8:1770915-1771520	MCF10A-Er-Src	breast:	n/a	n/a
4	POLR2A	chr8:1770733-1772156	MCF10A-Er-Src	breast:	n/a	n/a
5	STAT3	chr8:1771036-1771525	MCF10A-Er-Src	breast:	n/a	n/a
6	STAT3	chr8:1771062-1771504	MCF10A-Er-Src	breast:	n/a	n/a
7	MAFK	chr8:1771003-1771351	HepG2	liver:	n/a	chr8:1771171-1771186 chr8:1771170-1771184 chr8:1771171-1771187 chr8:1771171-1771182 chr8:1771171-1771182
8	MAFF	chr8:1771029-1771313	HepG2	liver:	n/a	chr8:1771169-1771187
9	RFX5	chr8:1771010-1772165	Hela-S3	cervix:	n/a	chr8:1771992-1772006
10	STAT3	chr8:1771025-1771528	MCF10A-Er-Src	breast:	n/a	n/a
11	MYC	chr8:1770856-1772169	MCF10A-Er-Src	breast:	n/a	chr8:1771949-1771962 chr8:1771950-1771960 chr8:1771614-1771624 chr8:1771949-1771962 chr8:1771951-1771960 chr8:1771562-1771572 chr8:1771950-1771960 chr8:1771951-1771961 chr8:1771950-1771961 chr8:1771950-1771961 chr8:1771951-1771961 chr8:1771891-1771901 chr8:1771950-1771961 chr8:1771640-1771650
12	MAX	chr8:1771110-1772330	HCT-116	colon:	n/a	chr8:1771949-1771962 chr8:1771950-1771960 chr8:1771614-1771624 chr8:1771949-1771962 chr8:1771951-1771960 chr8:1771562-1771572 chr8:1771950-1771960 chr8:1771951-1771961 chr8:1771950-1771961 chr8:1771950-1771961 chr8:1771951-1771961 chr8:1771891-1771901 chr8:1771950-1771961 chr8:1771640-1771650
13	MAFK	chr8:1770985-1771551	IMR90	lung:	n/a	chr8:1771171-1771186 chr8:1771170-1771184 chr8:1771171-1771187 chr8:1771171-1771182 chr8:1771171-1771182
14	MAZ	chr8:1771104-1772835	IMR90	lung:	n/a	chr8:1771949-1771962 chr8:1771950-1771960 chr8:1772502-1772512 chr8:1771614-1771624 chr8:1771949-1771962 chr8:1771951-1771960 chr8:1771562-1771572 chr8:1771950-1771960 chr8:1771951-1771961 chr8:1771950-1771961 chr8:1771950-1771961 chr8:1771951-1771961 chr8:1771891-1771901 chr8:1771950-1771961 chr8:1771640-1771650
15	MAFK	chr8:1770995-1771482	K562	blood:	n/a	chr8:1771171-1771186 chr8:1771170-1771184 chr8:1771171-1771187 chr8:1771171-1771182 chr8:1771171-1771182
16	MXI1	chr8:1770991-1772730	SK-N-SH	brain:	n/a	chr8:1771950-1771959 chr8:1771952-1771961 chr8:1771950-1771959 chr8:1771952-1771961
17	MAFK	chr8:1770831-1771508	Hela-S3	cervix:	n/a	chr8:1771171-1771186 chr8:1771170-1771184 chr8:1771171-1771187 chr8:1771171-1771182 chr8:1771171-1771182
18	FOS	chr8:1771078-1771499	MCF10A-Er-Src	breast:	n/a	chr8:1771481-1771495
19	MAFK	chr8:1771026-1771323	HepG2	liver:	n/a	chr8:1771171-1771186 chr8:1771170-1771184 chr8:1771171-1771187 chr8:1771171-1771182 chr8:1771171-1771182
20	MAX	chr8:1771097-1772384	A549	lung:	n/a	chr8:1771949-1771962 chr8:1771950-1771960 chr8:1771614-1771624 chr8:1771949-1771962 chr8:1771951-1771960 chr8:1771562-1771572 chr8:1771950-1771960 chr8:1771951-1771961 chr8:1771950-1771961 chr8:1771950-1771961 chr8:1771951-1771961 chr8:1771891-1771901 chr8:1771950-1771961 chr8:1771640-1771650

No.	Distal block	Cell Line	Cell type
1	chr8:1708451..1710291-chr8:1769924..1772142,2	K562	blood:
2	chr8:1709347..1712341-chr8:1770235..1771752,2	MCF-7	breast:
3	chr8:1764550..1766629-chr8:1770415..1772487,2	K562	blood:
4	chr8:1769937..1771639-chr8:1774044..1776450,2	MCF-7	breast:
5	chr8:1770355..1772056-chr8:1783670..1785482,2	MCF-7	breast:

Variant related genes	Relation type
ARHGEF10	TF binding region
ENSG00000104728	Chromatin interaction
ENSG00000182372	Chromatin interaction
ENSG00000253982	Chromatin interaction
ENSG00000207826	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs57819944	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61024005	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6558548	0.91[ASN][1000 genomes]
rs6980781	0.90[ASN][1000 genomes]
rs7018336	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7817199	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv889697	chr8:1238564-1861971	Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv889704	chr8:1563904-1965389	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv889707	chr8:1581839-1920461	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv889708	chr8:1581839-1965389	Genic enhancers Strong transcription Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv889709	chr8:1581839-1965389	Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	nsv889711	chr8:1591412-1904157	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
7	nsv889712	chr8:1591412-2337777	Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
8	nsv889714	chr8:1616718-1965389	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
9	nsv1034490	chr8:1654716-1782467	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
10	nsv532892	chr8:1687433-1839578	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
11	nsv465276	chr8:1701432-1777571	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
12	nsv609530	chr8:1701432-1777571	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
13	nsv609531	chr8:1717036-1965389	Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
14	nsv824454	chr8:1740369-1802873	Genic enhancers Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
15	nsv1025444	chr8:1743663-1864809	Genic enhancers Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
16	nsv539299	chr8:1743663-1864809	Active TSS Weak transcription Strong transcription Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
17	nsv470167	chr8:1746949-1886640	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
18	nsv465277	chr8:1746950-1888447	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
19	nsv609533	chr8:1746950-1888447	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
20	nsv889717	chr8:1746950-1924237	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
21	nsv889718	chr8:1748166-1807756	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
22	nsv1017597	chr8:1748941-1865887	Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
23	nsv889720	chr8:1756800-1811397	Enhancers Bivalent/Poised TSS Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	7 gene(s)	inside rSNPs	diseases
24	nsv889721	chr8:1756800-1815639	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	7 gene(s)	inside rSNPs	diseases
25	nsv889722	chr8:1756800-1857293	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats 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 miRNA target site	7 gene(s)	inside rSNPs	diseases
26	nsv889723	chr8:1756800-1904157	Enhancers Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
27	nsv889724	chr8:1756800-1965389	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
28	nsv1031464	chr8:1763119-1848596	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
29	nsv889725	chr8:1765371-1816527	Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	7 gene(s)	inside rSNPs	diseases
30	nsv824455	chr8:1767334-1772637	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
31	nsv889726	chr8:1768004-1798128	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
32	nsv889727	chr8:1768004-1815639	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent Enhancer Enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
33	nsv889728	chr8:1768004-1850622	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
34	esv3374295	chr8:1770970-1774918	Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
35	esv3323272	chr8:1771095-1774093	Bivalent Enhancer Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1762000-1771400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:1765600-1771200	Weak transcription	Right Atrium	heart
3	chr8:1765800-1771400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr8:1766200-1771200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr8:1766400-1771400	Weak transcription	Left Ventricle	heart
6	chr8:1766400-1771400	Weak transcription	Pancreas	Pancrea
7	chr8:1766600-1771600	Weak transcription	Spleen	Spleen
8	chr8:1766800-1771200	Weak transcription	NHEK	skin
9	chr8:1767800-1771600	Weak transcription	Gastric	stomach
10	chr8:1768600-1771400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr8:1768600-1771600	Weak transcription	Lung	lung
12	chr8:1768800-1771400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr8:1770400-1771200	Enhancers	Brain Anterior Caudate	brain
14	chr8:1770400-1771400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr8:1770600-1771200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr8:1770600-1771200	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr8:1770600-1771200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr8:1770800-1771200	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr8:1770800-1771200	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr8:1770800-1771200	Enhancers	Brain Cingulate Gyrus	brain
21	chr8:1770800-1771200	Enhancers	Hela-S3	cervix
22	chr8:1770800-1771200	Enhancers	HSMMtube	muscle
23	chr8:1770800-1771200	Enhancers	HUVEC	blood vessel
24	chr8:1770800-1771400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
25	chr8:1770800-1771400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr8:1770800-1771400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
27	chr8:1771000-1771200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr8:1771000-1771200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
29	chr8:1771000-1771200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
30	chr8:1771000-1771200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr8:1771000-1771200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr8:1771000-1771200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr8:1771000-1771200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr8:1771000-1771200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr8:1771000-1771200	Enhancers	Brain Hippocampus Middle	brain
36	chr8:1771000-1771200	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr8:1771000-1771200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr8:1771000-1771200	Bivalent Enhancer	Fetal Heart	heart
39	chr8:1771000-1771200	Bivalent Enhancer	Fetal Lung	lung
40	chr8:1771000-1771200	Flanking Active TSS	A549	lung
41	chr8:1771000-1771200	Enhancers	NHDF-Ad	bronchial
42	chr8:1771000-1771400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
43	chr8:1771000-1771400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
44	chr8:1771000-1771400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr8:1771000-1771400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
46	chr8:1771000-1771400	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr8:1771000-1771400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr8:1771000-1771400	Enhancers	Primary T killer memory cells from peripheral blood	blood
49	chr8:1771000-1771400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr8:1771000-1771400	Enhancers	Adipose Nuclei	Adipose

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