Variant report

Variant	rs149111634
Chromosome Location	chr14:67511960-67511961
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	chr14:67510207..67512789-chr14:67538433..67540909,2	K562	blood:

Extended variants
information (count: 17 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525460	chr14:66851185-67626594	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	esv1834170	chr14:67103140-67527235	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv2829998	chr14:67103579-67626594	Weak transcription Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv1838724	chr14:67232573-67527235	Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	esv2763071	chr14:67284476-67597237	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv902058	chr14:67310195-67760538	Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
7	nsv902059	chr14:67352226-67760538	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
8	esv2751285	chr14:67364747-67886781	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
9	nsv902060	chr14:67417083-67760538	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
10	esv1841498	chr14:67434470-67634318	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv564960	chr14:67449344-67549803	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv1038122	chr14:67487040-67528205	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	nsv977479	chr14:67506148-67513432	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3429238	chr14:67511271-67514262	Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv3434295	chr14:67511503-67512487	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
16	esv3448984	chr14:67511542-67512239	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv3331265	chr14:67511588-67512179	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:67511200-67512200	ZNF genes & repeats	GM12878-XiMat	blood
2	chr14:67511200-67512600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
3	chr14:67511600-67512400	Weak transcription	Fetal Kidney	kidney
4	chr14:67511600-67512600	Weak transcription	Brain Anterior Caudate	brain
5	chr14:67511600-67512800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
6	chr14:67511600-67514200	Weak transcription	Liver	Liver
7	chr14:67511600-67514600	Weak transcription	Osteobl	bone
8	chr14:67511600-67516600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr14:67511600-67516600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr14:67511600-67517000	Weak transcription	Dnd41	blood
11	chr14:67511600-67517200	Weak transcription	Ovary	ovary
12	chr14:67511600-67517400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr14:67511600-67517400	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr14:67511600-67517400	Weak transcription	Adipose Nuclei	Adipose
15	chr14:67511600-67517400	Weak transcription	Aorta	Aorta
16	chr14:67511600-67517400	Weak transcription	Esophagus	oesophagus
17	chr14:67511600-67517400	Weak transcription	Fetal Stomach	stomach
18	chr14:67511600-67517400	Weak transcription	Left Ventricle	heart
19	chr14:67511600-67517400	Weak transcription	Pancreas	Pancrea
20	chr14:67511600-67517400	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr14:67511600-67517600	Weak transcription	Duodenum Mucosa	Duodenum
22	chr14:67511600-67517600	Weak transcription	Spleen	Spleen
23	chr14:67511600-67517800	Weak transcription	Primary hematopoietic stem cells	blood
24	chr14:67511600-67517800	Weak transcription	Rectal Smooth Muscle	rectum
25	chr14:67511600-67517800	Weak transcription	Thymus	Thymus
26	chr14:67511600-67518200	Weak transcription	Hela-S3	cervix
27	chr14:67511600-67518400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr14:67511600-67518400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr14:67511600-67518400	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr14:67511600-67518400	Weak transcription	Right Ventricle	heart
31	chr14:67511600-67519000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr14:67511600-67519200	Weak transcription	Brain Substantia Nigra	brain
33	chr14:67511600-67519200	Weak transcription	Colon Smooth Muscle	Colon
34	chr14:67511600-67524000	Weak transcription	Gastric	stomach
35	chr14:67511600-67527200	Weak transcription	Brain Angular Gyrus	brain
36	chr14:67511600-67528800	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr14:67511600-67529000	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr14:67511600-67529400	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr14:67511600-67530200	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr14:67511600-67530400	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr14:67511600-67536000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr14:67511600-67538000	Weak transcription	Stomach Smooth Muscle	stomach
43	chr14:67511600-67544600	Weak transcription	Brain Hippocampus Middle	brain
44	chr14:67511600-67544800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr14:67511600-67556200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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