Variant report

Variant	rs60744960
Chromosome Location	chr22:33012617-33012618
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:33012442..33014400-chr22:33241656..33243487,2	K562	blood:
2	chr22:33012442..33015422-chr22:33150856..33153115,2	MCF-7	breast:

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10427961	1.00[ASN][1000 genomes]
rs16990837	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16990846	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16990851	0.93[ASN][1000 genomes]
rs16990852	1.00[ASN][1000 genomes]
rs17774399	0.83[EUR][1000 genomes]
rs3788467	0.82[EUR][1000 genomes]
rs57696440	1.00[ASN][1000 genomes]
rs59218864	1.00[ASN][1000 genomes]
rs60378048	0.82[EUR][1000 genomes]
rs60966625	0.88[EUR][1000 genomes]
rs62232743	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62232744	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62232752	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62232753	0.82[EUR][1000 genomes]
rs9784225	0.86[EUR][1000 genomes];0.88[ASN][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	nsv1055541	chr22:33006967-33101138	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	esv2762119	chr22:33006967-33101150	Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:33010400-33013000	Weak transcription	Fetal Kidney	kidney
2	chr22:33010400-33017400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr22:33011400-33015800	Enhancers	Fetal Stomach	stomach
4	chr22:33011600-33015000	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr22:33011600-33015200	Enhancers	Fetal Muscle Trunk	muscle
6	chr22:33011600-33015200	Enhancers	Fetal Muscle Leg	muscle
7	chr22:33011800-33012800	Flanking Active TSS	HepG2	liver
8	chr22:33011800-33013000	Enhancers	Left Ventricle	heart
9	chr22:33011800-33014400	Enhancers	Placenta Amnion	Placenta Amnion
10	chr22:33011800-33015200	Weak transcription	Hela-S3	cervix
11	chr22:33012000-33016000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr22:33012200-33012800	Weak transcription	Esophagus	oesophagus
13	chr22:33012200-33012800	Weak transcription	Right Ventricle	heart
14	chr22:33012200-33013400	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr22:33012200-33013400	Weak transcription	Small Intestine	intestine
16	chr22:33012200-33013800	Weak transcription	Psoas Muscle	Psoas
17	chr22:33012200-33014400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr22:33012400-33013000	Enhancers	Spleen	Spleen
19	chr22:33012400-33017600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr22:33012400-33017800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr22:33012400-33018400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr22:33012600-33013000	Weak transcription	Placenta	Placenta
23	chr22:33012600-33013200	Enhancers	Colon Smooth Muscle	Colon
24	chr22:33012600-33013600	Weak transcription	Adipose Nuclei	Adipose
25	chr22:33012600-33013600	Weak transcription	Rectal Smooth Muscle	rectum
26	chr22:33012600-33013600	Weak transcription	Right Atrium	heart
27	chr22:33012600-33014000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr22:33012600-33015800	Enhancers	Fetal Lung	lung
29	chr22:33012600-33017000	Weak transcription	Lung	lung
30	chr22:33012600-33017400	Weak transcription	Fetal Heart	heart

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