Variant report

Variant	rs8036916
Chromosome Location	chr15:35205399-35205400
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	chr15:35189106..35191007-chr15:35202848..35205608,2	K562	blood:
2	chr15:35202607..35205491-chr15:35208140..35210817,2	K562	blood:

Extended variants
information (count: 9 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3350109	chr15:34668106-35534229	Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv522411	chr15:34953986-35462981	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv457106	chr15:35049787-35227613	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv569153	chr15:35049787-35227613	Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	esv2761865	chr15:35101678-35271639	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv832967	chr15:35110102-35267906	Strong transcription Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv904071	chr15:35150897-35250771	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv904072	chr15:35150897-35259376	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv569154	chr15:35165366-35259376	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:35140400-35221600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr15:35186000-35206400	Weak transcription	Right Ventricle	heart
3	chr15:35186000-35206600	Weak transcription	Small Intestine	intestine
4	chr15:35186000-35212400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr15:35186000-35212600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr15:35186000-35213000	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr15:35186000-35220000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr15:35186000-35220000	Weak transcription	Pancreas	Pancrea
9	chr15:35186000-35223200	Weak transcription	Gastric	stomach
10	chr15:35186000-35232000	Weak transcription	Fetal Brain Male	brain
11	chr15:35186200-35212000	Strong transcription	Primary B cells from peripheral blood	blood
12	chr15:35186200-35212400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr15:35186200-35212400	Strong transcription	Liver	Liver
14	chr15:35186400-35205400	Weak transcription	Brain Cingulate Gyrus	brain
15	chr15:35186400-35238800	Strong transcription	Primary T helper cells fromperipheralblood	blood
16	chr15:35186600-35206000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr15:35186600-35212200	Strong transcription	Primary T cells fromperipheralblood	blood
18	chr15:35186600-35212200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr15:35186600-35212400	Strong transcription	HUES6 Cell Line	embryonic stem cell
20	chr15:35187200-35212000	Strong transcription	HUES64 Cell Line	embryonic stem cell
21	chr15:35187400-35212000	Strong transcription	Adipose Nuclei	Adipose
22	chr15:35191400-35212800	Strong transcription	HUES48 Cell Line	embryonic stem cell
23	chr15:35192000-35212200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr15:35192200-35211200	Strong transcription	Rectal Mucosa Donor 31	rectum
25	chr15:35192200-35212200	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr15:35192200-35212400	Strong transcription	Placenta	Placenta
27	chr15:35192400-35212000	Strong transcription	Duodenum Mucosa	Duodenum
28	chr15:35192400-35212400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr15:35192600-35212000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr15:35192600-35212400	Strong transcription	A549	lung
31	chr15:35193200-35206600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr15:35193400-35205400	Weak transcription	Osteobl	bone
33	chr15:35193800-35206400	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr15:35194200-35207600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr15:35195600-35208400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr15:35195800-35205800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr15:35196600-35207800	Strong transcription	Fetal Intestine Large	intestine
38	chr15:35196600-35211000	Strong transcription	Brain Inferior Temporal Lobe	brain
39	chr15:35197000-35207200	Strong transcription	Primary hematopoietic stem cells	blood
40	chr15:35197000-35211200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr15:35197200-35211000	Strong transcription	NH-A	brain
42	chr15:35197200-35212200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr15:35197200-35212600	Strong transcription	Primary T helper cells PMA-I stimulated	--
44	chr15:35197400-35211200	Strong transcription	Duodenum Smooth Muscle	Duodenum
45	chr15:35197400-35212000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr15:35197600-35207000	Strong transcription	NHDF-Ad	bronchial
47	chr15:35197600-35212200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr15:35197600-35212200	Strong transcription	Rectal Mucosa Donor 29	rectum
49	chr15:35197600-35212200	Strong transcription	Dnd41	blood
50	chr15:35197600-35238800	Strong transcription	Primary neutrophils fromperipheralblood	blood

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