Variant report

Variant	rs61991631
Chromosome Location	chr14:77687267-77687268
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	chr14:77687164..77689503-chr14:77690310..77692436,2	K562	blood:

Extended variants
information (count: 11 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv431017	chr14:76938089-77854647	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	107 gene(s)	inside rSNPs	diseases
2	nsv832834	chr14:77554987-77724357	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	esv3374587	chr14:77686224-77689072	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	esv3384702	chr14:77686549-77688947	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	esv3310810	chr14:77687130-77687652	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	esv3310811	chr14:77687130-77687652	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	esv3332071	chr14:77687144-77687800	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	esv3380878	chr14:77687159-77687735	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	esv3391787	chr14:77687197-77687696	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	esv3512806	chr14:77687207-77687636	Weak transcription Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	esv3512808	chr14:77687207-77687636	Weak transcription Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:77654200-77709400	Weak transcription	Esophagus	oesophagus
2	chr14:77680200-77688000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr14:77685000-77687400	Enhancers	H1 Cell Line	embryonic stem cell
4	chr14:77685000-77692800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr14:77685200-77690800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr14:77685400-77692600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr14:77685600-77688000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr14:77686000-77688200	Weak transcription	Fetal Brain Female	brain
9	chr14:77686400-77687400	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr14:77686400-77712400	Weak transcription	Brain Cingulate Gyrus	brain
11	chr14:77686600-77688800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr14:77686600-77689600	Weak transcription	Fetal Brain Male	brain
13	chr14:77686600-77690200	Weak transcription	Spleen	Spleen
14	chr14:77686600-77691800	Weak transcription	Fetal Intestine Small	intestine
15	chr14:77687000-77688000	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr14:77687000-77688000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr14:77687000-77688200	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr14:77687000-77688200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr14:77687000-77688600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr14:77687000-77688600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr14:77687000-77690000	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr14:77687000-77691400	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr14:77687000-77692000	Weak transcription	Brain Angular Gyrus	brain
24	chr14:77687000-77697000	Weak transcription	Brain Substantia Nigra	brain
25	chr14:77687000-77697200	Weak transcription	Brain Anterior Caudate	brain
26	chr14:77687000-77697800	Weak transcription	Pancreas	Pancrea
27	chr14:77687200-77688200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr14:77687200-77688400	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr14:77687200-77689000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr14:77687200-77692400	Weak transcription	Gastric	stomach

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