Variant report

Variant	rs2502637
Chromosome Location	chr6:144609700-144609701
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	chr6:144608193..144609848-chr6:144615238..144616857,2	K562	blood:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs2017652	0.96[EUR][1000 genomes]
rs2473130	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2473135	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2473136	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2473137	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2473138	0.89[CEU][hapmap];0.94[TSI][hapmap];0.96[EUR][1000 genomes]
rs2473139	0.89[CEU][hapmap];0.96[EUR][1000 genomes]
rs2473140	0.89[CEU][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes]
rs2473141	0.96[EUR][1000 genomes]
rs2473142	0.89[CEU][hapmap];0.96[EUR][1000 genomes]
rs2473143	0.96[EUR][1000 genomes]
rs2473144	0.96[EUR][1000 genomes]
rs2473146	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2473147	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs2473148	0.89[CEU][hapmap];0.93[EUR][1000 genomes]
rs2473149	0.89[CEU][hapmap];0.94[TSI][hapmap];0.93[EUR][1000 genomes]
rs2473150	0.91[EUR][1000 genomes]
rs2473151	0.94[TSI][hapmap];0.88[EUR][1000 genomes]
rs2502628	0.89[CEU][hapmap];0.96[EUR][1000 genomes]
rs2502630	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2502631	0.91[EUR][1000 genomes]
rs2502634	0.88[GIH][hapmap];1.00[MEX][hapmap];0.89[AMR][1000 genomes]
rs2502635	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2502638	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2502639	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2502642	0.90[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs2502643	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830831	chr6:144501371-144649509	Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv830832	chr6:144572378-144759023	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv2422260	chr6:144574591-144731630	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1031253	chr6:144599055-144883013	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv538461	chr6:144599055-144883013	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:144608400-144626600	Weak transcription	Spleen	Spleen
2	chr6:144608600-144610000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:144608600-144610200	Weak transcription	Lung	lung
4	chr6:144608600-144610600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr6:144608600-144612600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr6:144608600-144613000	Weak transcription	Placenta	Placenta
7	chr6:144608600-144613400	Weak transcription	Fetal Muscle Trunk	muscle
8	chr6:144608600-144616600	Weak transcription	Pancreas	Pancrea
9	chr6:144608600-144616800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:144608600-144617200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr6:144608600-144617200	Weak transcription	Gastric	stomach
12	chr6:144608600-144617800	Weak transcription	Stomach Mucosa	stomach
13	chr6:144608600-144619400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr6:144608600-144626800	Weak transcription	Esophagus	oesophagus
15	chr6:144608600-144629800	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr6:144608600-144631400	Weak transcription	Colonic Mucosa	Colon
17	chr6:144608800-144610400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr6:144608800-144616800	Weak transcription	Fetal Intestine Large	intestine
19	chr6:144608800-144617600	Weak transcription	Right Atrium	heart
20	chr6:144609000-144614000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr6:144609000-144616400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr6:144609000-144616800	Weak transcription	Aorta	Aorta
23	chr6:144609200-144610000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr6:144609200-144610400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr6:144609200-144610400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr6:144609200-144612000	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr6:144609200-144612200	Weak transcription	Liver	Liver
28	chr6:144609200-144612200	Weak transcription	Ovary	ovary
29	chr6:144609200-144612400	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr6:144609200-144612600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr6:144609200-144612800	Weak transcription	Primary hematopoietic stem cells	blood
32	chr6:144609200-144613400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr6:144609200-144613400	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr6:144609200-144613400	Weak transcription	HSMMtube	muscle
35	chr6:144609200-144613400	Weak transcription	NHLF	lung
36	chr6:144609200-144614400	Weak transcription	NHEK	skin
37	chr6:144609200-144616000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr6:144609200-144616400	Weak transcription	Fetal Muscle Leg	muscle
39	chr6:144609200-144616400	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr6:144609200-144616600	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr6:144609200-144616600	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr6:144609200-144616600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr6:144609200-144616600	Weak transcription	Left Ventricle	heart
44	chr6:144609200-144616800	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr6:144609200-144616800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr6:144609200-144616800	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr6:144609200-144616800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr6:144609200-144616800	Weak transcription	Fetal Lung	lung
49	chr6:144609200-144616800	Weak transcription	Fetal Stomach	stomach
50	chr6:144609200-144617000	Weak transcription	Right Ventricle	heart

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