Variant report

Variant	rs372610702
Chromosome Location	chr10:5738912-5738913
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr10:5738874-5739007	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:5724274..5728540-chr10:5734829..5741563,8	MCF-7	breast:
2	chr10:5585750..5587884-chr10:5738818..5740542,2	K562	blood:
3	chr10:5726410..5728417-chr10:5738015..5741917,3	MCF-7	breast:
4	chr10:5737326..5739856-chr10:5853864..5856173,2	MCF-7	breast:
5	chr10:5733360..5736300-chr10:5737628..5741126,5	MCF-7	breast:

Variant related genes	Relation type
FAM208B	TF binding region
ENSG00000108021	Chromatin interaction
ENSG00000272764	Chromatin interaction
ENSG00000057608	Chromatin interaction

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	nsv534685	chr10:4914018-5853324	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
2	esv2759729	chr10:5557024-5804780	Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	esv2758209	chr10:5637111-5804780	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
4	esv1796213	chr10:5716555-5766165	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv522415	chr10:5721653-5768493	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	esv34147	chr10:5726821-6105717	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
7	esv34061	chr10:5726821-6225187	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
8	nsv1050663	chr10:5737979-5785918	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5728800-5746800	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr10:5734800-5763400	Weak transcription	HSMM	muscle
3	chr10:5735200-5739000	Weak transcription	Fetal Intestine Large	intestine
4	chr10:5735200-5739400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr10:5735200-5739400	Weak transcription	Lung	lung
6	chr10:5735200-5739400	Weak transcription	Pancreas	Pancrea
7	chr10:5735200-5739800	Enhancers	Primary T killer memory cells from peripheral blood	blood
8	chr10:5735200-5743000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
9	chr10:5735200-5749000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr10:5735200-5750600	Weak transcription	Gastric	stomach
11	chr10:5735200-5767000	Weak transcription	Fetal Muscle Leg	muscle
12	chr10:5735400-5739200	Weak transcription	Fetal Heart	heart
13	chr10:5735400-5739200	Weak transcription	Fetal Intestine Small	intestine
14	chr10:5735400-5739400	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr10:5735400-5739400	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr10:5735400-5739400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr10:5735400-5739600	Weak transcription	Colonic Mucosa	Colon
18	chr10:5735400-5744800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr10:5735400-5750800	Weak transcription	Spleen	Spleen
20	chr10:5735400-5761600	Weak transcription	NHEK	skin
21	chr10:5735400-5762000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr10:5735600-5739000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr10:5735800-5739000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr10:5735800-5741800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr10:5735800-5752800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr10:5736000-5739600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr10:5736200-5739200	Weak transcription	Thymus	Thymus
28	chr10:5736200-5739400	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr10:5736200-5739600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr10:5736200-5740000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr10:5736200-5740200	Weak transcription	A549	lung
32	chr10:5736200-5742600	Weak transcription	Brain Angular Gyrus	brain
33	chr10:5736200-5751600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr10:5736400-5739000	Weak transcription	Duodenum Mucosa	Duodenum
35	chr10:5736400-5739200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr10:5736400-5741000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr10:5736400-5753000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr10:5736600-5739000	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr10:5736600-5741600	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr10:5736800-5739400	Weak transcription	Primary B cells from peripheral blood	blood
41	chr10:5736800-5742000	Weak transcription	Primary T cells from cord blood	blood
42	chr10:5736800-5742000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr10:5737000-5739200	Weak transcription	Stomach Mucosa	stomach
44	chr10:5737000-5742000	Weak transcription	Brain Substantia Nigra	brain
45	chr10:5737000-5742600	Weak transcription	Brain Hippocampus Middle	brain
46	chr10:5737000-5743600	Weak transcription	Primary hematopoietic stem cells	blood
47	chr10:5737400-5739400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr10:5737400-5744200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
49	chr10:5737400-5744800	Weak transcription	Liver	Liver
50	chr10:5737600-5740200	Enhancers	HepG2	liver

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