Variant report

Variant	nsv1037778
Chromosome Location	chr10:51886486-52011986
allele	n/a
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	ARID3A	chr10:51976432-51976444	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:52011227-52011506	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:51994435-51994634	HepG2	liver:	n/a	n/a
4	BATF	chr10:51932652-51932839	GM12878	blood:	n/a	chr10:51932736-51932747
5	BATF	chr10:51991390-51991694	GM12878	blood:	n/a	n/a
6	BATF	chr10:51922567-51922785	GM12878	blood:	n/a	n/a
7	BATF	chr10:51984168-51984477	GM12878	blood:	n/a	n/a
8	BATF	chr10:51984190-51984474	GM12878	blood:	n/a	n/a
9	BCL11A	chr10:51991318-51991679	GM12878	blood:	n/a	n/a
10	BHLHE40	chr10:51903317-51903550	HepG2	liver:	n/a	n/a
11	CEBPB	chr10:52009901-52010147	HepG2	liver:	n/a	chr10:52010013-52010024
12	CEBPB	chr10:51922602-51922774	K562	blood:	n/a	chr10:51922715-51922724 chr10:51922715-51922724 chr10:51922715-51922724 chr10:51922715-51922724 chr10:51922713-51922726 chr10:51922715-51922726
13	CEBPB	chr10:52009830-52010200	HepG2	liver:	n/a	chr10:52010013-52010024
14	CEBPB	chr10:52009838-52010190	HepG2	liver:	n/a	chr10:52010013-52010024
15	CEBPB	chr10:52001086-52001319	HepG2	liver:	n/a	n/a
16	CEBPB	chr10:52009948-52010148	K562	blood:	n/a	chr10:52010013-52010024
17	CEBPB	chr10:52009832-52010221	HepG2	liver:	n/a	chr10:52010013-52010024
18	CEBPB	chr10:52010481-52010795	HepG2	liver:	n/a	n/a
19	CEBPB	chr10:51922509-51922875	K562	blood:	n/a	chr10:51922715-51922724 chr10:51922715-51922724 chr10:51922715-51922724 chr10:51922715-51922724 chr10:51922713-51922726 chr10:51922715-51922726
20	CEBPD	chr10:52009943-52010168	HepG2	liver:	n/a	n/a
21	CTCF	chr10:51984178-51984402	LNCaP	prostate:	n/a	chr10:51984272-51984290 chr10:51984267-51984288
22	CTCF	chr10:51897106-51897155	GM13977	blood:	n/a	n/a
23	CTCF	chr10:51984184-51984406	MCF-7	breast:	n/a	chr10:51984272-51984290 chr10:51984267-51984288
24	CTCF	chr10:51984169-51984459	K562	blood:	n/a	chr10:51984272-51984290 chr10:51984267-51984288
25	CTCF	chr10:51902238-51902253	GM10266	blood:	n/a	n/a
26	CTCF	chr10:51928329-51928352	GM10248	blood:	n/a	n/a
27	CTCF	chr10:51984191-51984384	MCF-7	breast:	n/a	chr10:51984272-51984290 chr10:51984267-51984288
28	CTCF	chr10:51959902-51960064	LNCaP	prostate:	n/a	n/a
29	CTCF	chr10:51984187-51984424	GM13976	blood:	n/a	chr10:51984272-51984290 chr10:51984267-51984288
30	CTCF	chr10:51984157-51984366	A549	lung:	n/a	chr10:51984272-51984290 chr10:51984267-51984288
31	CTCF	chr10:51924895-51924996	GM13976	blood:	n/a	chr10:51924952-51924973 chr10:51924950-51924968 chr10:51924951-51924967
32	CTCF	chr10:51924828-51925017	K562	blood:	n/a	chr10:51924952-51924973 chr10:51924950-51924968 chr10:51924951-51924967
33	CTCF	chr10:51984170-51984428	Medullo	brain:	n/a	chr10:51984272-51984290 chr10:51984267-51984288
34	CTCF	chr10:51959920-51959998	Pancreas_OC	pancreas:	n/a	n/a
35	CTCF	chr10:52006360-52006510	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr10:51984189-51984387	MCF-7	breast:	n/a	chr10:51984272-51984290 chr10:51984267-51984288
37	CTCF	chr10:51924876-51925024	GM13977	blood:	n/a	chr10:51924952-51924973 chr10:51924950-51924968 chr10:51924951-51924967
38	CTCF	chr10:51956419-51956524	GM10266	blood:	n/a	n/a
39	CTCF	chr10:51890791-51890836	GM13977	blood:	n/a	n/a
40	CTCF	chr10:51902967-51903051	GM20000	blood:	n/a	n/a
41	CTCF	chr10:51887691-51888009	K562	blood:	n/a	chr10:51887834-51887847 chr10:51887827-51887848 chr10:51887872-51887885 chr10:51887816-51887824 chr10:51887832-51887850 chr10:51887817-51887825 chr10:51887837-51887846 chr10:51887872-51887885
42	CTCF	chr10:51924918-51925048	MCF-7	breast:	n/a	chr10:51924952-51924973 chr10:51924950-51924968 chr10:51924951-51924967
43	CTCF	chr10:51887674-51888040	K562	blood:	n/a	chr10:51887834-51887847 chr10:51887827-51887848 chr10:51887872-51887885 chr10:51887816-51887824 chr10:51887832-51887850 chr10:51887817-51887825 chr10:51887837-51887846 chr10:51887872-51887885
44	CTCF	chr10:51984183-51984367	Lung_OC	lung:	n/a	chr10:51984272-51984290 chr10:51984267-51984288
45	CTCF	chr10:51984146-51984434	A549	lung:	n/a	chr10:51984272-51984290 chr10:51984267-51984288
46	CTCF	chr10:51971258-51971321	GM13976	blood:	n/a	n/a
47	CTCF	chr10:51924853-51925057	LNCaP	prostate:	n/a	chr10:51924952-51924973 chr10:51924950-51924968 chr10:51924951-51924967
48	CTCF	chr10:51984176-51984403	Pancreas_OC	pancreas:	n/a	chr10:51984272-51984290 chr10:51984267-51984288
49	CTCF	chr10:51981900-51981969	GM10266	blood:	n/a	n/a
50	CTCF	chr10:51903262-51903355	Pancreas_OC	pancreas:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:52008593-52008643	HPAEpiC	pulmonary alveolar:	n/a
2	chr10:52002547-52002597	PANC-1	pancreas:	n/a
3	chr10:51912805-51912855	NHDF-neo	bronchial:	n/a
4	chr10:52008905-52008955	AoSMC	blood vessel:	n/a
5	chr10:52002547-52002597	NT2-D1	testis:	n/a
6	chr10:51912631-51912681	HepG2	liver:	n/a
7	chr10:52008593-52008643	A549	lung:	n/a
8	chr10:52008805-52008855	GM19239	blood:	n/a
9	chr10:52008593-52008643	RPTEC	kidney:	n/a
10	chr10:52008905-52008955	HEEpiC	esophagus:	n/a
11	chr10:51912805-51912855	MCF10A-Er-Src	breast:	n/a
12	chr10:51912805-51912855	HNPCEpiC	eye:	n/a
13	chr10:51912805-51912855	SKMC	muscle:	n/a
14	chr10:52008593-52008643	CMK	blood:	n/a
15	chr10:52008593-52008643	AoSMC	blood vessel:	n/a
16	chr10:51911889-51911939	Hepatocyte	liver:	n/a
17	chr10:52002547-52002597	HCM	heart:	n/a
18	chr10:51911889-51911939	GM06990	blood:	n/a
19	chr10:52002547-52002597	AG10803	skin:	n/a
20	chr10:51912805-51912855	HEK293	kidney:	embryo
21	chr10:52008360-52008410	AG04450	lung:	fetal
22	chr10:51911889-51911939	Jurkat	blood:	n/a
23	chr10:52008805-52008855	AG04450	lung:	fetal
24	chr10:52008905-52008955	U87	brain:	n/a
25	chr10:52008360-52008410	GM06990	blood:	n/a
26	chr10:52008805-52008855	HRE	kidney:	n/a
27	chr10:51912631-51912681	AoSMC	blood vessel:	n/a
28	chr10:52008805-52008855	K562	blood:	n/a
29	chr10:52002547-52002597	A549	lung:	n/a
30	chr10:51912805-51912855	HIPEpiC	eye:	n/a
31	chr10:51912805-51912855	ProgFib	skin:	n/a
32	chr10:52008360-52008410	HEK293	kidney:	embryo
33	chr10:51912631-51912681	BJ	skin:	n/a
34	chr10:51912631-51912681	ECC-1	luminal epithelium:	n/a
35	chr10:52002547-52002597	HNPCEpiC	eye:	n/a
36	chr10:52008905-52008955	HAEpiC	amniotic membrane:	n/a
37	chr10:52008593-52008643	HCPEpiC	choroid plexus:	n/a
38	chr10:51912805-51912855	Hepatocyte	liver:	n/a
39	chr10:52008805-52008855	AG10803	skin:	n/a
40	chr10:51912805-51912855	SAEC	small airway:	n/a
41	chr10:52008593-52008643	HUVEC	blood vessel:	n/a
42	chr10:52008905-52008955	IMR90	lung:	fetal
43	chr10:52008905-52008955	NT2-D1	testis:	n/a
44	chr10:51911889-51911939	PFSK-1	brain:	n/a
45	chr10:51912805-51912855	HMEC	breast:	n/a
46	chr10:52008805-52008855	GM12878	blood:	n/a
47	chr10:51912631-51912681	H1-hESC	embryonic stem cell:	embryo
48	chr10:52008805-52008855	NT2-D1	testis:	n/a
49	chr10:52008905-52008955	HepG2	liver:	n/a
50	chr10:51911889-51911939	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:52001284..52004039-chr10:52006500..52009846,3	K562	blood:
2	chr10:52011614..52013335-chr10:52018420..52020373,2	K562	blood:
3	chr10:52009441..52011844-chr10:52036005..52038580,2	K562	blood:

Variant related genes	Relation type
SLC9A3P1	TF binding region
ASAH2	TF binding region
SLC9A3P1	CpG island
ASAH2	CpG island
ENSG00000188611	chromatin interactions

Extended variants
information (count: 655 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:655 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112443072	chr10:51887422-51887423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs576736035	chr10:51887542-51887543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545487967	chr10:51887719-51887720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529234090	chr10:51888096-51888097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556179695	chr10:51888121-51888122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576105998	chr10:51888272-51888273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542038255	chr10:51888332-51888333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561900215	chr10:51888369-51888370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs2669768	chr10:51888388-51888389	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs527563138	chr10:51888389-51888390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs2669767	chr10:51888402-51888403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186788091	chr10:51888412-51888413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191637429	chr10:51888440-51888441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111572410	chr10:51888443-51888444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549954343	chr10:51888482-51888483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs2338072	chr10:51888557-51888558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185858514	chr10:51888562-51888563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549142641	chr10:51888809-51888810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565905383	chr10:51888829-51888830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534901899	chr10:51888841-51888842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551614909	chr10:51888863-51888864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571848189	chr10:51888997-51888998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539418336	chr10:51889019-51889020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555929154	chr10:51889111-51889112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190172043	chr10:51889145-51889146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371353909	chr10:51889146-51889147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374910730	chr10:51889157-51889158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535574375	chr10:51889182-51889183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555524419	chr10:51889183-51889184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572237385	chr10:51889189-51889190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370231804	chr10:51889211-51889212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541237468	chr10:51889321-51889322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564359168	chr10:51889375-51889376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs577899274	chr10:51889614-51889615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543782780	chr10:51889815-51889816	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563559800	chr10:51889817-51889818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529269673	chr10:51889904-51889905	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549029968	chr10:51889926-51889927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562663957	chr10:51890369-51890370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559427087	chr10:51890458-51890459	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528612236	chr10:51890477-51890478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs78369021	chr10:51890577-51890578	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs372236284	chr10:51890666-51890667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376582947	chr10:51890677-51890678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112307181	chr10:51891701-51891702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551736593	chr10:51891881-51891882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375311421	chr10:51891914-51891915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571902761	chr10:51891923-51891924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537380370	chr10:51891976-51891977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549730219	chr10:51892193-51892194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
Autism	21948486	CNVD
speech delay	21948486	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:51828600-51891800	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr10:51828600-51893400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr10:51828800-51889800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr10:51836400-51894000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr10:51852800-51892000	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr10:51858400-51891000	Weak transcription	Adipose Nuclei	Adipose
7	chr10:51869000-51891400	Weak transcription	Duodenum Mucosa	Duodenum
8	chr10:51872000-51891400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr10:51878000-51891600	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr10:51883200-51895000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr10:51889000-51891400	Weak transcription	Stomach Smooth Muscle	stomach
12	chr10:51889800-51890600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr10:51890200-51893000	Weak transcription	Osteobl	bone
14	chr10:51890600-51892200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr10:51892800-51895600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr10:51912600-51913000	Active TSS	Brain Germinal Matrix	brain
17	chr10:51977000-51977600	Enhancers	HepG2	liver
18	chr10:51977600-51978000	Weak transcription	HepG2	liver
19	chr10:51978000-51978400	Enhancers	HepG2	liver
20	chr10:52000000-52002000	Weak transcription	Fetal Intestine Small	intestine
21	chr10:52000000-52003000	Weak transcription	Duodenum Mucosa	Duodenum
22	chr10:52002000-52002200	Strong transcription	Fetal Intestine Small	intestine
23	chr10:52002200-52002400	Bivalent Enhancer	K562	blood
24	chr10:52002200-52002800	Weak transcription	Fetal Intestine Small	intestine
25	chr10:52002400-52003800	Enhancers	K562	blood
26	chr10:52002800-52003000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr10:52002800-52003000	Bivalent Enhancer	A549	lung
28	chr10:52002800-52003800	Strong transcription	Fetal Intestine Small	intestine
29	chr10:52003000-52003200	Enhancers	Duodenum Mucosa	Duodenum
30	chr10:52003000-52005200	Enhancers	Fetal Intestine Large	intestine
31	chr10:52003200-52003600	Weak transcription	Duodenum Mucosa	Duodenum
32	chr10:52003600-52004400	Enhancers	Duodenum Mucosa	Duodenum
33	chr10:52003800-52004200	Bivalent Enhancer	K562	blood
34	chr10:52003800-52005200	Genic enhancers	Fetal Intestine Small	intestine
35	chr10:52003800-52005200	Enhancers	Small Intestine	intestine
36	chr10:52004000-52004600	Enhancers	HepG2	liver
37	chr10:52004400-52006600	Weak transcription	Duodenum Mucosa	Duodenum
38	chr10:52004600-52007400	Weak transcription	HepG2	liver
39	chr10:52005200-52006400	Weak transcription	Fetal Intestine Small	intestine
40	chr10:52005200-52007200	Weak transcription	Fetal Intestine Large	intestine
41	chr10:52005200-52007600	Weak transcription	Small Intestine	intestine
42	chr10:52006400-52006600	Enhancers	Fetal Intestine Small	intestine
43	chr10:52006600-52007000	Weak transcription	Fetal Intestine Small	intestine
44	chr10:52006600-52007600	Enhancers	Duodenum Mucosa	Duodenum
45	chr10:52007000-52008800	Enhancers	Fetal Intestine Small	intestine
46	chr10:52007200-52009600	Enhancers	Fetal Intestine Large	intestine
47	chr10:52007400-52010000	Enhancers	HepG2	liver
48	chr10:52007400-52010200	Enhancers	Liver	Liver
49	chr10:52007600-52007800	Enhancers	Small Intestine	intestine
50	chr10:52007600-52009000	Flanking Active TSS	Duodenum Mucosa	Duodenum

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