Variant report

Variant	rs4244151
Chromosome Location	chr1:61709546-61709547
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:61705176..61707440-chr1:61708242..61713126,6	K562	blood:
2	chr1:61706948..61709963-chr1:61716553..61719225,3	K562	blood:

Variant related genes	Relation type
ENSG00000237853	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs12082781	1.00[YRI][hapmap]
rs162878	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs167987	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17121858	0.82[CHB][hapmap];0.83[ASN][1000 genomes]
rs186742	0.81[AMR][1000 genomes]
rs2275208	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs333136	1.00[CEU][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs333138	0.87[AMR][1000 genomes]
rs333140	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs333141	0.81[EUR][1000 genomes]
rs333142	1.00[CEU][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs333143	0.92[JPT][hapmap]
rs333144	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs333145	1.00[CEU][hapmap];0.92[JPT][hapmap];0.82[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs333146	0.92[JPT][hapmap]
rs333147	1.00[CEU][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs333148	1.00[CEU][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs333150	1.00[CEU][hapmap];0.87[AMR][1000 genomes]
rs333160	1.00[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs333161	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs333162	1.00[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs333164	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs333165	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs333166	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs334690	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6684051	1.00[CEU][hapmap]
rs72664877	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1849929	chr1:61684084-61714142	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv994970	chr1:61693951-62199657	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv1006142	chr1:61696142-62119763	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh 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
4	nsv534980	chr1:61696142-62119763	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent Enhancer Genic enhancers 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 target site	6 gene(s)	inside rSNPs	diseases
5	nsv916868	chr1:61700430-62119762	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers 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 target site	6 gene(s)	inside rSNPs	diseases
6	nsv1001052	chr1:61702011-62090670	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer 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 target site	3 gene(s)	inside rSNPs	diseases
7	nsv817402	chr1:61703965-62119762	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers 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 target site	6 gene(s)	inside rSNPs	diseases
8	nsv1010797	chr1:61703966-62125970	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers 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	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:61680000-61720200	Weak transcription	Fetal Muscle Trunk	muscle
2	chr1:61703600-61713600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr1:61704600-61713400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr1:61704600-61713600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr1:61705400-61715200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr1:61706600-61710400	Enhancers	Liver	Liver
7	chr1:61706800-61710400	Enhancers	HepG2	liver
8	chr1:61707000-61709800	Weak transcription	NHDF-Ad	bronchial
9	chr1:61707000-61710200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr1:61707200-61713400	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr1:61707400-61718800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr1:61707400-61718800	Weak transcription	Gastric	stomach
13	chr1:61707600-61709600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr1:61707600-61709800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr1:61707600-61709800	Weak transcription	Esophagus	oesophagus
16	chr1:61707600-61709800	Weak transcription	HMEC	breast
17	chr1:61707600-61709800	Weak transcription	Osteobl	bone
18	chr1:61707600-61710000	Weak transcription	Brain Cingulate Gyrus	brain
19	chr1:61707600-61710200	Enhancers	Fetal Heart	heart
20	chr1:61707600-61719000	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr1:61707800-61709600	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr1:61707800-61709800	Weak transcription	Right Ventricle	heart
23	chr1:61707800-61710400	Enhancers	Brain Anterior Caudate	brain
24	chr1:61707800-61710400	Enhancers	Fetal Brain Male	brain
25	chr1:61707800-61718600	Weak transcription	Stomach Mucosa	stomach
26	chr1:61708000-61709600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr1:61708000-61709600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr1:61708000-61709600	Weak transcription	Brain Angular Gyrus	brain
29	chr1:61708000-61709800	Weak transcription	Aorta	Aorta
30	chr1:61708000-61709800	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr1:61708000-61709800	Weak transcription	Brain Substantia Nigra	brain
32	chr1:61708000-61709800	Weak transcription	Fetal Brain Female	brain
33	chr1:61708000-61709800	Weak transcription	Fetal Muscle Leg	muscle
34	chr1:61708000-61709800	Weak transcription	Left Ventricle	heart
35	chr1:61708000-61709800	Weak transcription	Ovary	ovary
36	chr1:61708000-61709800	Weak transcription	Pancreas	Pancrea
37	chr1:61708000-61709800	Weak transcription	Psoas Muscle	Psoas
38	chr1:61708000-61709800	Weak transcription	Right Atrium	heart
39	chr1:61708000-61709800	Weak transcription	K562	blood
40	chr1:61708000-61710000	Weak transcription	Small Intestine	intestine
41	chr1:61708000-61710000	Weak transcription	NHLF	lung
42	chr1:61708000-61710200	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr1:61708000-61710400	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr1:61708000-61710400	Enhancers	Rectal Smooth Muscle	rectum
45	chr1:61708000-61710800	Enhancers	Fetal Lung	lung
46	chr1:61708000-61712200	Enhancers	Colon Smooth Muscle	Colon
47	chr1:61708000-61712800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr1:61708000-61713600	Weak transcription	A549	lung
49	chr1:61708000-61718800	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr1:61708000-61720400	Weak transcription	Colonic Mucosa	Colon

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