Variant report

Variant	rs373681885
Chromosome Location	chr10:25241585-25241586
allele	A/G
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	chr10:25241440-25241590	HVMF	connective:	n/a	n/a
2	POLR2A	chr10:25241135-25241597	Hela-S3	cervix:	n/a	n/a
3	POLR2A	chr10:25240578-25242391	MCF-7	breast:	n/a	n/a
4	POLR2A	chr10:25241086-25242108	A549	lung:	n/a	n/a
5	YY1	chr10:25241328-25241636	SK-N-SH	brain:	n/a	n/a
6	MAX	chr10:25240852-25242106	GM12878	blood:	n/a	n/a
7	ZBTB7A	chr10:25241279-25242084	ECC-1	luminal epithelium:	n/a	chr10:25241694-25241703
8	CTCF	chr10:25241440-25241590	HCM	heart:	n/a	n/a
9	POLR2A	chr10:25241076-25242194	A549	lung:	n/a	n/a
10	EGR1	chr10:25241579-25242255	H1-hESC	embryonic stem cell:	n/a	chr10:25241695-25241705 chr10:25241841-25241851 chr10:25241694-25241707 chr10:25241715-25241728 chr10:25241803-25241817
11	ELF1	chr10:25241574-25241926	GM12878	blood:	n/a	chr10:25241802-25241811 chr10:25241835-25241847 chr10:25241869-25241882
12	E2F6	chr10:25240834-25242460	A549	lung:	n/a	chr10:25241284-25241296 chr10:25241518-25241529 chr10:25241751-25241760 chr10:25241720-25241729 chr10:25241517-25241529 chr10:25241842-25241851 chr10:25241284-25241293 chr10:25241831-25241841 chr10:25241535-25241547 chr10:25241803-25241813 chr10:25241536-25241547
13	POLR2A	chr10:25240181-25244662	K562	blood:	n/a	n/a
14	CTCF	chr10:25241156-25242031	GM12878	blood:	n/a	chr10:25241805-25241823 chr10:25241806-25241822 chr10:25241807-25241820
15	POLR2A	chr10:25241412-25241728	H1-neurons	neurons:	n/a	n/a
16	BHLHE40	chr10:25240622-25242272	GM12878	blood:	n/a	chr10:25241832-25241848 chr10:25241803-25241819 chr10:25241723-25241739 chr10:25241792-25241808
17	ELF1	chr10:25241562-25242028	K562	blood:	n/a	chr10:25241802-25241811 chr10:25241835-25241847 chr10:25241869-25241882
18	POLR2A	chr10:25241097-25242083	A549	lung:	n/a	n/a
19	TAF1	chr10:25241303-25241660	SK-N-SH	brain:	n/a	n/a
20	UBTF	chr10:25240562-25242561	K562	blood:	n/a	n/a
21	CTCF	chr10:25241460-25241610	HA-sp	spinal cord:	n/a	n/a
22	CTCF	chr10:25241369-25242065	K562	blood:	n/a	chr10:25241805-25241823 chr10:25241806-25241822 chr10:25241807-25241820
23	CHD1	chr10:25241037-25241874	GM12878	blood:	n/a	chr10:25241723-25241733 chr10:25241285-25241295
24	MYC	chr10:25241216-25241593	MCF-7	breast:	n/a	n/a
25	E2F6	chr10:25240562-25242230	H1-hESC	embryonic stem cell:	n/a	chr10:25241284-25241296 chr10:25241518-25241529 chr10:25241751-25241760 chr10:25241720-25241729 chr10:25241517-25241529 chr10:25241842-25241851 chr10:25241284-25241293 chr10:25241831-25241841 chr10:25241535-25241547 chr10:25241803-25241813 chr10:25241536-25241547
26	MAX	chr10:25240488-25242348	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr10:25241390-25241592	NHEK	skin:	n/a	n/a
28	MYC	chr10:25240350-25242595	K562	blood:	n/a	n/a
29	POLR2A	chr10:25240548-25242157	Gliobla	brain:	n/a	n/a
30	CHD2	chr10:25241080-25242215	Hela-S3	cervix:	n/a	chr10:25241723-25241733 chr10:25241285-25241295
31	CTCF	chr10:25241394-25241596	MCF-7	breast:	n/a	n/a
32	ZNF143	chr10:25240297-25242230	H1-hESC	embryonic stem cell:	n/a	chr10:25240833-25240851 chr10:25241686-25241696
33	HMGN3	chr10:25240572-25242067	K562	blood:	n/a	n/a
34	POLR2A	chr10:25240291-25242512	K562	blood:	n/a	n/a
35	SIN3A	chr10:25240309-25242360	H1-hESC	embryonic stem cell:	n/a	chr10:25241794-25241807 chr10:25242209-25242218
36	CTCF	chr10:25241460-25241610	NHDF-neo	bronchial:	n/a	n/a
37	UBTF	chr10:25240600-25242563	K562	blood:	n/a	n/a
38	POLR2A	chr10:25241167-25241599	MCF-7	breast:	n/a	n/a
39	POLR2A	chr10:25241294-25242149	SK-N-MC	brain:	n/a	n/a
40	ZMIZ1	chr10:25240569-25242628	K562	blood:	n/a	n/a
41	YY1	chr10:25240644-25242186	K562	blood:	n/a	chr10:25241842-25241851 chr10:25241803-25241817 chr10:25241837-25241851 chr10:25241805-25241814 chr10:25241284-25241293 chr10:25241797-25241811 chr10:25241834-25241848 chr10:25241714-25241723 chr10:25241802-25241811
42	POLR2A	chr10:25240583-25242147	GM19099	blood:	n/a	n/a
43	MYC	chr10:25240599-25242486	K562	blood:	n/a	n/a
44	MAX	chr10:25241251-25241667	MCF-7	breast:	n/a	n/a
45	ZC3H11A	chr10:25241386-25241604	K562	blood:	n/a	n/a
46	POLR2A	chr10:25240175-25242598	H1-hESC	embryonic stem cell:	n/a	n/a
47	RAD21	chr10:25241254-25242131	A549	lung:	n/a	chr10:25241700-25241710 chr10:25241806-25241819 chr10:25241805-25241817 chr10:25241803-25241822 chr10:25241807-25241817
48	CTCF	chr10:25241440-25241590	GM12864	blood:	n/a	n/a
49	SMC3	chr10:25240491-25242275	Hela-S3	cervix:	n/a	chr10:25241807-25241821 chr10:25241807-25241817
50	CHD2	chr10:25240555-25242218	K562	blood:	n/a	chr10:25241723-25241733 chr10:25241285-25241295

No.	Distal block	Cell Line	Cell type
1	chr10:25010748..25013945-chr10:25238648..25242767,8	MCF-7	breast:
2	chr10:25010212..25016288-chr10:25239162..25243925,7	K562	blood:
3	chr10:25009845..25014059-chr10:25240930..25243462,5	MCF-7	breast:
4	chr10:25009082..25014020-chr10:25238727..25242865,5	K562	blood:
5	chr10:25239628..25245194-chr10:25304841..25307327,7	K562	blood:

Variant related genes	Relation type
PRTFDC1	TF binding region
ENSG00000273107	TF binding region
ENSG00000185875	Chromatin interaction
ENSG00000107863	Chromatin interaction
ENSG00000151023	Chromatin interaction

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1053278	chr10:25140776-25269093	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv3433843	chr10:25240746-25242744	Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25240200-25243000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr10:25240400-25242600	Active TSS	H9 Cell Line	embryonic stem cell
3	chr10:25240400-25242600	Flanking Active TSS	Dnd41	blood
4	chr10:25240600-25241600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr10:25240600-25241600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr10:25240600-25242400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
7	chr10:25240600-25242400	Active TSS	Rectal Mucosa Donor 29	rectum
8	chr10:25240600-25242400	Active TSS	Rectal Smooth Muscle	rectum
9	chr10:25240600-25242600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr10:25240600-25242600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
11	chr10:25240600-25242600	Active TSS	Pancreatic Islets	Pancreatic Islet
12	chr10:25240800-25241600	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
13	chr10:25240800-25241800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr10:25240800-25241800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr10:25240800-25241800	Active TSS	Rectal Mucosa Donor 31	rectum
16	chr10:25240800-25242000	Active TSS	Primary T helper naive cells from peripheral blood	blood
17	chr10:25240800-25242000	Active TSS	Brain Angular Gyrus	brain
18	chr10:25240800-25242000	Active TSS	Brain Substantia Nigra	brain
19	chr10:25240800-25242200	Active TSS	HUES64 Cell Line	embryonic stem cell
20	chr10:25240800-25242200	Active TSS	iPS-18 Cell Line	embryonic stem cell
21	chr10:25240800-25242200	Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr10:25240800-25242200	Active TSS	Fetal Kidney	kidney
23	chr10:25240800-25242200	Active TSS	Fetal Lung	lung
24	chr10:25240800-25242200	Active TSS	Hela-S3	cervix
25	chr10:25240800-25242400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr10:25240800-25242600	Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr10:25240800-25242600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr10:25241000-25241600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
29	chr10:25241000-25241600	Flanking Active TSS	Placenta	Placenta
30	chr10:25241000-25241800	Active TSS	Primary T cells from cord blood	blood
31	chr10:25241000-25241800	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
32	chr10:25241000-25242000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr10:25241000-25242000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
34	chr10:25241000-25242000	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
35	chr10:25241000-25242000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr10:25241000-25242000	Active TSS	Brain Anterior Caudate	brain
37	chr10:25241000-25242000	Active TSS	Brain Cingulate Gyrus	brain
38	chr10:25241000-25242000	Active TSS	Brain Hippocampus Middle	brain
39	chr10:25241000-25242000	Active TSS	Colon Smooth Muscle	Colon
40	chr10:25241000-25242000	Active TSS	Duodenum Mucosa	Duodenum
41	chr10:25241000-25242000	Enhancers	Fetal Brain Male	brain
42	chr10:25241000-25242000	Active TSS	Fetal Brain Female	brain
43	chr10:25241000-25242000	Active TSS	Fetal Intestine Large	intestine
44	chr10:25241000-25242000	Active TSS	Fetal Stomach	stomach
45	chr10:25241000-25242000	Active TSS	Gastric	stomach
46	chr10:25241000-25242000	Active TSS	Pancreas	Pancrea
47	chr10:25241000-25242000	Active TSS	Psoas Muscle	Psoas
48	chr10:25241000-25242000	Active TSS	Sigmoid Colon	Sigmoid Colon
49	chr10:25241000-25242000	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
50	chr10:25241000-25242000	Active TSS	A549	lung

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