Variant report

Variant	rs7517173
Chromosome Location	chr1:220167218-220167219
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:220165101..220168556-chr1:220168858..220170933,3	K562	blood:
2	chr1:220164810..220167759-chr1:220168424..220170636,2	K562	blood:
3	chr1:220166855..220169233-chr1:220184126..220185704,2	K562	blood:

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12134746	0.86[ASN][1000 genomes]
rs36122746	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs41274788	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41304103	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5030752	0.89[CHB][hapmap];0.86[ASN][1000 genomes]
rs5030754	0.89[CHB][hapmap];0.86[ASN][1000 genomes]
rs6541124	1.00[CHB][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs6683340	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6690630	0.89[CHB][hapmap];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv427930	chr1:220120379-220333434	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers 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 miRNA miRNA target site	744 gene(s)	inside rSNPs	diseases
2	nsv998124	chr1:220132739-220189211	Strong transcription Weak transcription Active TSS Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	n/a
3	nsv832636	chr1:220139697-220294352	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats 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 miRNA target site	738 gene(s)	inside rSNPs	diseases
4	esv1798515	chr1:220157811-220167371	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:220132800-220177000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:220140000-220167400	Weak transcription	Gastric	stomach
3	chr1:220140800-220173400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr1:220140800-220192400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr1:220141200-220192200	Weak transcription	Fetal Kidney	kidney
6	chr1:220142600-220169400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr1:220146400-220182800	Weak transcription	Spleen	Spleen
8	chr1:220147200-220169400	Weak transcription	Fetal Heart	heart
9	chr1:220149000-220167400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:220149400-220178200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr1:220153600-220169200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr1:220154200-220169200	Weak transcription	Fetal Brain Male	brain
13	chr1:220154400-220169200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr1:220154400-220169200	Weak transcription	Fetal Lung	lung
15	chr1:220154600-220169000	Weak transcription	Small Intestine	intestine
16	chr1:220154600-220169200	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr1:220154800-220167400	Weak transcription	Pancreas	Pancrea
18	chr1:220155600-220168600	Weak transcription	Brain Substantia Nigra	brain
19	chr1:220156800-220169800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr1:220157000-220168800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr1:220157200-220177200	Weak transcription	Esophagus	oesophagus
22	chr1:220158200-220177200	Weak transcription	Right Ventricle	heart
23	chr1:220159200-220168800	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr1:220159800-220169200	Weak transcription	Colonic Mucosa	Colon
25	chr1:220160200-220168600	Weak transcription	Brain Hippocampus Middle	brain
26	chr1:220160400-220167400	Weak transcription	Primary B cells from cord blood	blood
27	chr1:220160400-220168600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr1:220160800-220169200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr1:220160800-220174200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr1:220161000-220167400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr1:220161000-220168800	Weak transcription	Colon Smooth Muscle	Colon
32	chr1:220161000-220168800	Weak transcription	Thymus	Thymus
33	chr1:220161000-220169200	Weak transcription	Psoas Muscle	Psoas
34	chr1:220161000-220169200	Weak transcription	NHLF	lung
35	chr1:220161200-220168800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr1:220161200-220169200	Weak transcription	Left Ventricle	heart
37	chr1:220161600-220168800	Weak transcription	Primary hematopoietic stem cells	blood
38	chr1:220161800-220168800	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr1:220162000-220167400	Weak transcription	Fetal Muscle Trunk	muscle
40	chr1:220162000-220168600	Weak transcription	Brain Cingulate Gyrus	brain
41	chr1:220162000-220168800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr1:220162000-220168800	Weak transcription	Brain Angular Gyrus	brain
43	chr1:220162000-220169200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr1:220162000-220169200	Weak transcription	Rectal Smooth Muscle	rectum
45	chr1:220162000-220175600	Weak transcription	Placenta Amnion	Placenta Amnion
46	chr1:220162200-220168400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr1:220162200-220168800	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr1:220162200-220168800	Weak transcription	HMEC	breast
49	chr1:220162200-220169000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr1:220162200-220169400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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