Variant report

Variant	rs8100128
Chromosome Location	chr19:38633990-38633991
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:38633389..38636227-chr19:38637615..38640869,3	K562	blood:
2	chr19:38633263..38636587-chr19:38638025..38640526,3	K562	blood:
3	chr19:38625391..38627747-chr19:38633636..38636533,2	MCF-7	breast:
4	chr19:38629908..38632279-chr19:38632364..38634124,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10404957	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1725489	1.00[YRI][hapmap]
rs2005055	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2099340	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2278429	0.85[CEU][hapmap]
rs2384778	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2569412	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs332843	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs332844	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs332848	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs332849	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs332850	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs332851	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs332855	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs332856	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs332858	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs332864	1.00[CEU][hapmap];0.82[JPT][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35932728	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4802251	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6508765	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs705507	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs8100144	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs8101826	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs8109695	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs8109799	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs8111180	1.00[CEU][hapmap];0.82[JPT][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs8112798	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs855614	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs855632	0.89[CEU][hapmap];0.83[JPT][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9941474	1.00[CEU][hapmap];0.83[JPT][hapmap];0.83[YRI][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949296	chr19:38034722-38763140	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv833821	chr19:38629937-38756792	Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:38591800-38642800	Weak transcription	Small Intestine	intestine
2	chr19:38600600-38652800	Weak transcription	NHDF-Ad	bronchial
3	chr19:38610800-38643600	Weak transcription	HepG2	liver
4	chr19:38611000-38652800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr19:38611600-38634400	Weak transcription	Stomach Mucosa	stomach
6	chr19:38611600-38634800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr19:38611600-38634800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr19:38611600-38641400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr19:38611600-38653000	Weak transcription	HUVEC	blood vessel
10	chr19:38611800-38634600	Weak transcription	NH-A	brain
11	chr19:38611800-38642600	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr19:38611800-38653000	Weak transcription	Fetal Kidney	kidney
13	chr19:38613400-38634400	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr19:38613600-38634800	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr19:38613800-38635600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr19:38613800-38636600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr19:38613800-38639000	Weak transcription	Left Ventricle	heart
18	chr19:38613800-38641800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr19:38613800-38643200	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr19:38613800-38652200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr19:38613800-38652600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr19:38614000-38634800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr19:38616000-38652600	Strong transcription	Primary B cells from peripheral blood	blood
24	chr19:38616200-38641600	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr19:38616600-38642000	Weak transcription	Dnd41	blood
26	chr19:38617000-38652000	Strong transcription	Fetal Intestine Small	intestine
27	chr19:38618200-38651000	Strong transcription	Fetal Intestine Large	intestine
28	chr19:38619600-38647800	Strong transcription	Fetal Stomach	stomach
29	chr19:38621600-38642800	Weak transcription	NHLF	lung
30	chr19:38621800-38634000	Weak transcription	Thymus	Thymus
31	chr19:38622000-38634600	Weak transcription	Brain Germinal Matrix	brain
32	chr19:38622200-38636800	Weak transcription	Brain Anterior Caudate	brain
33	chr19:38622400-38634000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr19:38622600-38641800	Weak transcription	Aorta	Aorta
35	chr19:38622800-38634000	Weak transcription	Rectal Smooth Muscle	rectum
36	chr19:38622800-38634600	Weak transcription	Adipose Nuclei	Adipose
37	chr19:38622800-38634800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr19:38623000-38635200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr19:38623000-38642800	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr19:38623200-38634400	Weak transcription	Fetal Brain Female	brain
41	chr19:38624400-38652400	Weak transcription	Fetal Thymus	thymus
42	chr19:38626000-38643400	Weak transcription	Placenta	Placenta
43	chr19:38626200-38634600	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr19:38626400-38634400	Weak transcription	Right Ventricle	heart
45	chr19:38626400-38635200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr19:38626400-38642000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr19:38626400-38643400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr19:38626400-38652200	Strong transcription	A549	lung
49	chr19:38626600-38634000	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr19:38626600-38635600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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