Variant report

Variant	rs148243209
Chromosome Location	chr10:43903732-43903733
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	MXI1	chr10:43902185-43905112	HepG2	liver:	n/a	chr10:43904301-43904316
2	POLR2A	chr10:43901067-43905573	HL-60	blood:	n/a	n/a
3	CHD2	chr10:43903627-43903872	HepG2	liver:	n/a	n/a
4	MXI1	chr10:43902599-43905102	Hela-S3	cervix:	n/a	chr10:43904301-43904316
5	RAD21	chr10:43903560-43903863	SK-N-SH_RA	brain:	n/a	chr10:43903656-43903668 chr10:43903686-43903696
6	IRF1	chr10:43902895-43905077	K562	blood:	n/a	chr10:43904331-43904345 chr10:43904091-43904105 chr10:43904518-43904532 chr10:43904669-43904683 chr10:43904347-43904361 chr10:43903277-43903291
7	MAFK	chr10:43903086-43903789	K562	blood:	n/a	n/a
8	CTCF	chr10:43903542-43903792	H1-hESC	embryonic stem cell:	n/a	chr10:43903683-43903696 chr10:43903683-43903692
9	POLR2A	chr10:43903530-43904061	A549	lung:	n/a	n/a
10	CTCF	chr10:43903600-43903750	A549	lung:	n/a	chr10:43903683-43903696 chr10:43903683-43903692
11	HA-E2F1	chr10:43902310-43903874	MCF-7	breast:	n/a	chr10:43903002-43903012 chr10:43902697-43902708 chr10:43902678-43902688 chr10:43902908-43902920 chr10:43902675-43902685
12	CTCF	chr10:43903504-43903879	K562	blood:	n/a	chr10:43903683-43903696 chr10:43903683-43903692
13	TEAD4	chr10:43902955-43903985	K562	blood:	n/a	n/a
14	MAX	chr10:43902163-43905172	K562	blood:	n/a	chr10:43904307-43904316 chr10:43903332-43903343 chr10:43903333-43903342 chr10:43904402-43904411 chr10:43903767-43903774
15	CTCF	chr10:43903680-43903830	WI-38	lung:	n/a	chr10:43903683-43903696 chr10:43903683-43903692
16	PBX3	chr10:43902976-43904025	A549	lung:	n/a	n/a
17	HDAC2	chr10:43903579-43904732	K562	blood:	n/a	n/a
18	CTCF	chr10:43903600-43903750	GM12874	blood:	n/a	chr10:43903683-43903696 chr10:43903683-43903692
19	CTCF	chr10:43903620-43903770	NHDF-neo	bronchial:	n/a	chr10:43903683-43903696 chr10:43903683-43903692
20	STAT5A	chr10:43902981-43903767	GM12878	blood:	n/a	chr10:43903301-43903308
21	POLR2A	chr10:43903647-43903880	A549	lung:	n/a	n/a
22	IRF1	chr10:43901288-43903827	K562	blood:	n/a	chr10:43902647-43902661 chr10:43903277-43903291
23	POLR2A	chr10:43901131-43905953	HepG2	liver:	n/a	n/a
24	JUN	chr10:43902090-43905336	K562	blood:	n/a	chr10:43902652-43902661 chr10:43904977-43904986
25	SMARCB1	chr10:43902578-43905702	Hela-S3	cervix:	n/a	n/a
26	POLR2A	chr10:43902530-43905094	HepG2	liver:	n/a	n/a
27	SETDB1	chr10:43903129-43905501	K562	blood:	n/a	chr10:43904422-43904446
28	MAX	chr10:43903036-43903899	HepG2	liver:	n/a	chr10:43903332-43903343 chr10:43903333-43903342 chr10:43903767-43903774
29	NR2F2	chr10:43902718-43904036	K562	blood:	n/a	n/a
30	POLR2A	chr10:43902517-43905565	GM12891	blood:	n/a	n/a
31	CTCF	chr10:43903622-43903740	MCF-7	breast:	n/a	chr10:43903683-43903696 chr10:43903683-43903692
32	SIN3AK20	chr10:43902854-43905693	HCT-116	colon:	n/a	n/a
33	POLR2A	chr10:43901150-43905187	K562	blood:	n/a	n/a
34	E2F6	chr10:43902545-43905260	K562	blood:	n/a	chr10:43903002-43903012 chr10:43904863-43904870 chr10:43902697-43902708 chr10:43904932-43904949 chr10:43904863-43904870 chr10:43902678-43902688 chr10:43902908-43902920 chr10:43902675-43902685 chr10:43904863-43904870 chr10:43904730-43904745 chr10:43904670-43904679
35	PML	chr10:43902951-43903917	MCF-7	breast:	n/a	n/a
36	CTCF	chr10:43903606-43903759	A549	lung:	n/a	chr10:43903683-43903696 chr10:43903683-43903692
37	POLR2A	chr10:43900942-43905753	GM12878	blood:	n/a	n/a
38	MAX	chr10:43902831-43905956	HCT-116	colon:	n/a	chr10:43904307-43904316 chr10:43903332-43903343 chr10:43903333-43903342 chr10:43904402-43904411 chr10:43903767-43903774
39	CTCF	chr10:43903575-43903798	GM12891	blood:	n/a	chr10:43903683-43903696 chr10:43903683-43903692
40	CTCF	chr10:43903600-43903750	K562	blood:	n/a	chr10:43903683-43903696 chr10:43903683-43903692
41	CTCF	chr10:43903640-43903790	GM12871	blood:	n/a	chr10:43903683-43903696 chr10:43903683-43903692
42	BCLAF1	chr10:43902934-43903888	K562	blood:	n/a	chr10:43902997-43903010 chr10:43903647-43903656 chr10:43903001-43903014
43	POLR2A	chr10:43902445-43905122	GM12891	blood:	n/a	n/a
44	MAX	chr10:43903121-43905142	K562	blood:	n/a	chr10:43904307-43904316 chr10:43903332-43903343 chr10:43903333-43903342 chr10:43904402-43904411 chr10:43903767-43903774
45	MAX	chr10:43902453-43905428	A549	lung:	n/a	chr10:43904307-43904316 chr10:43903332-43903343 chr10:43903333-43903342 chr10:43904402-43904411 chr10:43903767-43903774
46	ATF2	chr10:43902934-43903817	GM12878	blood:	n/a	n/a
47	CEBPB	chr10:43902918-43903980	HCT-116	colon:	n/a	n/a
48	CTCF	chr10:43903600-43903750	HRE	kidney:	n/a	chr10:43903683-43903696 chr10:43903683-43903692
49	CTCF	chr10:43903640-43903790	SAEC	small airway:	n/a	chr10:43903683-43903696 chr10:43903683-43903692
50	POLR2A	chr10:43902392-43905656	GM12892	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:28834319..28834870-chr10:43903446..43904273,2	Hela-S3	cervix:
2	chr10:43867647..43875264-chr10:43900659..43906151,11	MCF-7	breast:
3	chr10:43902834..43905281-chr10:44101183..44103050,2	MCF-7	breast:
4	chr10:43901751..43904156-chr7:26239345..26241405,2	K562	blood:
5	chr10:43903142..43903814-chr16:67207852..67208622,2	Hela-S3	cervix:
6	chr1:153507944..153508640-chr10:43903183..43903757,2	Hela-S3	cervix:
7	chr10:43903162..43904071-chr16:68002331..68002833,2	Hela-S3	cervix:
8	chr10:43901370..43906375-chr10:43928042..43934083,16	MCF-7	breast:
9	chr10:43903270..43903785-chr19:36139022..36139531,2	HCT-116	colon:
10	chr10:43903380..43903891-chr5:6712551..6713349,2	Hela-S3	cervix:
11	chr10:43901784..43908257-chr10:43928243..43934263,17	MCF-7	breast:
12	chr10:43899870..43905980-chr10:43953401..43957689,7	MCF-7	breast:
13	chr10:43903427..43904398-chr20:43594621..43595269,2	Hela-S3	cervix:
14	chr10:43903376..43903911-chr17:62501886..62502819,2	Hela-S3	cervix:
15	chr10:43902951..43903891-chr11:62439137..62439806,2	NB4	blood:
16	chr10:43903244..43904543-chr10:43931320..43932838,6	Hela-S3	cervix:
17	chr10:43902635..43905319-chr11:65265113..65267204,2	K562	blood:
18	chr10:43901770..43904893-chr10:44100789..44103373,5	MCF-7	breast:
19	chr10:43696064..43699246-chr10:43901638..43904576,3	K562	blood:
20	chr10:43887055..43906178-chr10:43946385..43955803,85	K562	blood:
21	chr10:43696835..43700131-chr10:43902185..43905182,4	K562	blood:
22	chr10:43902596..43905009-chr12:7053130..7055096,2	K562	blood:

Variant related genes	Relation type
HNRNPF	TF binding region
ENSG00000111678	Chromatin interaction
ENSG00000101109	Chromatin interaction
ENSG00000150201	Chromatin interaction
ENSG00000122565	Chromatin interaction
ENSG00000272173	Chromatin interaction
ENSG00000198298	Chromatin interaction
ENSG00000270117	Chromatin interaction
ENSG00000227477	Chromatin interaction
ENSG00000162194	Chromatin interaction
ENSG00000197956	Chromatin interaction
ENSG00000140939	Chromatin interaction
ENSG00000232004	Chromatin interaction
ENSG00000243660	Chromatin interaction
ENSG00000122566	Chromatin interaction
ENSG00000126267	Chromatin interaction
ENSG00000258890	Chromatin interaction
ENSG00000108654	Chromatin interaction
ENSG00000252532	Chromatin interaction
ENSG00000124067	Chromatin interaction
ENSG00000198915	Chromatin interaction
ENSG00000251562	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	nsv430159	chr10:43291894-43946294	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
2	nsv895087	chr10:43783339-43982390	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
3	nsv831842	chr10:43846541-43987501	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
4	nsv895088	chr10:43871999-44003101	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
5	nsv825354	chr10:43883418-43949936	Flanking Active TSS Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
6	nsv825355	chr10:43890579-43923802	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
7	nsv825356	chr10:43893080-43946515	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	63 gene(s)	inside rSNPs	diseases
8	esv3395522	chr10:43903571-43906119	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	38 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43900200-43904600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
2	chr10:43900800-43905600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr10:43901000-43905800	Active TSS	HSMM	muscle
4	chr10:43901200-43904000	Flanking Active TSS	Primary hematopoietic stem cells	blood
5	chr10:43901200-43904400	Flanking Active TSS	Primary B cells from cord blood	blood
6	chr10:43901200-43905200	Active TSS	Small Intestine	intestine
7	chr10:43901200-43905800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr10:43901400-43905000	Active TSS	HMEC	breast
9	chr10:43901400-43905200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr10:43901400-43905400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
11	chr10:43901400-43905400	Active TSS	Primary T helper cells PMA-I stimulated	--
12	chr10:43901400-43905400	Active TSS	Ovary	ovary
13	chr10:43901400-43905600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr10:43901400-43905800	Active TSS	Pancreatic Islets	Pancreatic Islet
15	chr10:43901600-43905400	Active TSS	H1 Cell Line	embryonic stem cell
16	chr10:43901600-43905400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr10:43901600-43905400	Active TSS	Gastric	stomach
18	chr10:43901600-43905600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr10:43901600-43905600	Active TSS	HUES48 Cell Line	embryonic stem cell
20	chr10:43901600-43905600	Active TSS	iPS-15b Cell Line	embryonic stem cell
21	chr10:43901600-43905600	Active TSS	iPS-18 Cell Line	embryonic stem cell
22	chr10:43901600-43905600	Active TSS	Primary T killer memory cells from peripheral blood	blood
23	chr10:43901600-43905600	Active TSS	Right Atrium	heart
24	chr10:43901600-43905600	Active TSS	GM12878-XiMat	blood
25	chr10:43901600-43905600	Active TSS	HSMMtube	muscle
26	chr10:43901600-43905600	Active TSS	NHDF-Ad	bronchial
27	chr10:43901600-43905600	Active TSS	NHLF	lung
28	chr10:43901600-43905800	Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr10:43901600-43905800	Active TSS	HUES64 Cell Line	embryonic stem cell
30	chr10:43901600-43906000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr10:43901800-43905000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr10:43901800-43905000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr10:43901800-43905000	Active TSS	Breast Myoepithelial Primary Cells	Breast
34	chr10:43901800-43905000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr10:43901800-43905200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr10:43901800-43905400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
37	chr10:43901800-43905400	Active TSS	Primary T helper naive cells from peripheral blood	blood
38	chr10:43901800-43905400	Active TSS	Liver	Liver
39	chr10:43901800-43905400	Active TSS	Esophagus	oesophagus
40	chr10:43901800-43905400	Active TSS	Fetal Intestine Large	intestine
41	chr10:43901800-43905400	Active TSS	Fetal Intestine Small	intestine
42	chr10:43901800-43905400	Active TSS	Sigmoid Colon	Sigmoid Colon
43	chr10:43901800-43905400	Active TSS	Stomach Mucosa	stomach
44	chr10:43901800-43905400	Active TSS	Hela-S3	cervix
45	chr10:43901800-43905600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr10:43901800-43905600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr10:43901800-43905600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr10:43901800-43905800	Active TSS	H9 Cell Line	embryonic stem cell
49	chr10:43901800-43905800	Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr10:43901800-43905800	Active TSS	Duodenum Smooth Muscle	Duodenum

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