Variant report

Variant	rs141751773
Chromosome Location	chr8:61688477-61688478
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	chr8:61687942..61689827-chr8:61698388..61701380,2	K562	blood:
2	chr8:61681233..61684163-chr8:61687430..61689381,2	K562	blood:

Extended variants
information (count: 8 )
Associated
traits (count: 0)

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	nsv917756	chr8:60942299-61862796	Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
2	nsv831335	chr8:61497540-61688992	Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv890945	chr8:61522008-61707725	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv526196	chr8:61593569-61877623	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	nsv1022801	chr8:61623974-61738067	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
6	nsv539632	chr8:61623974-61738067	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
7	esv1797364	chr8:61658362-61696231	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	esv3337994	chr8:61687698-61692296	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 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	chr8:61657000-61690400	Weak transcription	HepG2	liver
2	chr8:61672000-61694400	Weak transcription	A549	lung
3	chr8:61672200-61693400	Weak transcription	Hela-S3	cervix
4	chr8:61672200-61694000	Weak transcription	HUVEC	blood vessel
5	chr8:61677000-61691800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr8:61680000-61698600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr8:61680200-61694800	Weak transcription	Lung	lung
8	chr8:61680200-61694800	Weak transcription	K562	blood
9	chr8:61680200-61696200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr8:61680200-61704200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr8:61680200-61705200	Weak transcription	Esophagus	oesophagus
12	chr8:61680200-61710400	Weak transcription	Pancreas	Pancrea
13	chr8:61680400-61689400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr8:61680400-61694600	Weak transcription	Placenta	Placenta
15	chr8:61681000-61694400	Weak transcription	HSMMtube	muscle
16	chr8:61681200-61693600	Weak transcription	Fetal Muscle Trunk	muscle
17	chr8:61681200-61693600	Weak transcription	Fetal Muscle Leg	muscle
18	chr8:61681200-61694800	Weak transcription	Gastric	stomach
19	chr8:61681200-61696200	Weak transcription	Right Ventricle	heart
20	chr8:61681200-61698600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr8:61681200-61700400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr8:61681200-61705200	Weak transcription	Spleen	Spleen
23	chr8:61681400-61693600	Weak transcription	Dnd41	blood
24	chr8:61682200-61705200	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr8:61682600-61688600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr8:61682600-61690800	Weak transcription	Stomach Mucosa	stomach
27	chr8:61682600-61694800	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr8:61683400-61694000	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr8:61683600-61691400	Weak transcription	Fetal Intestine Large	intestine
30	chr8:61683600-61711200	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr8:61683800-61692800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr8:61683800-61693800	Weak transcription	Duodenum Mucosa	Duodenum
33	chr8:61683800-61695800	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr8:61684000-61688600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr8:61684000-61692200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr8:61684200-61689000	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr8:61685000-61688800	Weak transcription	Primary B cells from cord blood	blood
38	chr8:61685200-61691800	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr8:61685200-61704200	Weak transcription	Small Intestine	intestine
40	chr8:61686000-61692600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr8:61686000-61698600	Weak transcription	Fetal Intestine Small	intestine
42	chr8:61686200-61693600	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr8:61686200-61693600	Weak transcription	HSMM	muscle
44	chr8:61686200-61694400	Weak transcription	Duodenum Smooth Muscle	Duodenum
45	chr8:61686200-61694800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr8:61686200-61694800	Weak transcription	Rectal Smooth Muscle	rectum
47	chr8:61686400-61689200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr8:61686600-61691400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr8:61686800-61688800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr8:61686800-61689000	Weak transcription	Primary T helper cells fromperipheralblood	blood

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