Variant report

Variant	nsv591932
Chromosome Location	chr3:144968890-145174583
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:31)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:145047302..145049061-chr3:145051775..145054184,2	K562	blood:
2	chr3:144984029..144984834-chr3:145416240..145416755,2	MCF-7	breast:
3	chr3:145061451..145063891-chr3:145082446..145084868,2	K562	blood:
4	chr3:144968846..144970924-chr3:144975225..144978166,2	MCF-7	breast:
5	chr3:145070588..145072380-chr3:145074616..145076227,2	MCF-7	breast:
6	chr3:145089993..145092059-chr3:145098025..145100330,2	MCF-7	breast:
7	chr3:144983651..144984522-chr3:145123095..145123660,2	MCF-7	breast:
8	chr3:145072717..145074625-chr3:145076447..145079320,2	MCF-7	breast:
9	chr3:145011656..145013483-chr3:145013706..145015700,2	MCF-7	breast:
10	chr3:145151670..145153633-chr3:145165383..145167143,2	K562	blood:
11	chr3:145063874..145066771-chr3:145068629..145070450,2	K562	blood:
12	chr3:144983996..144984506-chr3:145485486..145486139,2	MCF-7	breast:
13	chr3:145047302..145049061-chr3:145051775..145054184,2	K562	blood:
14	chr3:145113957..145115664-chr3:145117395..145120125,2	MCF-7	breast:
15	chr3:144983651..144984522-chr3:145123095..145123660,2	MCF-7	breast:
16	chr3:145021934..145024791-chr3:145028136..145030465,2	K562	blood:
17	chr3:145083751..145085344-chr3:145088911..145090506,2	K562	blood:
18	chr3:145011656..145013483-chr3:145013706..145015700,2	MCF-7	breast:
19	chr3:145006504..145009118-chr3:145011068..145013301,2	MCF-7	breast:
20	chr3:145021934..145024791-chr3:145028136..145030465,2	K562	blood:
21	chr3:145151670..145153633-chr3:145165383..145167143,2	K562	blood:
22	chr3:144968846..144970924-chr3:144975225..144978166,2	MCF-7	breast:
23	chr3:145072717..145074625-chr3:145076447..145079320,2	MCF-7	breast:
24	chr3:145061451..145063891-chr3:145082446..145084868,2	K562	blood:
25	chr3:144984069..144984806-chr3:145485343..145486312,4	MCF-7	breast:
26	chr3:145083751..145085344-chr3:145088911..145090506,2	K562	blood:
27	chr3:145089993..145092059-chr3:145098025..145100330,2	MCF-7	breast:
28	chr3:145113957..145115664-chr3:145117395..145120125,2	MCF-7	breast:
29	chr3:145070588..145072380-chr3:145074616..145076227,2	MCF-7	breast:
30	chr3:145006504..145009118-chr3:145011068..145013301,2	MCF-7	breast:
31	chr3:145063874..145066771-chr3:145068629..145070450,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC107021.1-9	chr3:145093215-145098582	NONHSAT092537
2	lnc-AC107021.1-9	chr3:145091512-145091541	NONHSAT092537

No data

Extended variants
information (count: 2950 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2950 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12637929	chr3:144968890-144968891	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs149488955	chr3:144969037-144969038	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs186465690	chr3:144969044-144969045	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs554900864	chr3:144969075-144969076	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs73016185	chr3:144969079-144969080	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs373977451	chr3:144969113-144969114	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs143911331	chr3:144969115-144969116	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs563248177	chr3:144969125-144969126	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs190453062	chr3:144969130-144969131	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs573365047	chr3:144969133-144969134	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs549028660	chr3:144969160-144969161	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs79115613	chr3:144969162-144969163	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs528201289	chr3:144969232-144969233	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs547571677	chr3:144969252-144969253	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs565975426	chr3:144969266-144969267	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs553484248	chr3:144969293-144969294	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs565565496	chr3:144969294-144969295	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs540126302	chr3:144969312-144969313	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs1445369	chr3:144969313-144969314	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs569997759	chr3:144969331-144969332	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs537068836	chr3:144969338-144969339	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs555824353	chr3:144969347-144969348	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs17822933	chr3:144969409-144969410	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs62274761	chr3:144969428-144969429	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs553199906	chr3:144969430-144969431	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs373751095	chr3:144969453-144969454	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs376658933	chr3:144969459-144969460	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs371865889	chr3:144969460-144969461	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs575149040	chr3:144969550-144969551	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs542195967	chr3:144969587-144969588	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs148666834	chr3:144969606-144969607	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs375040270	chr3:144969612-144969613	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs528166152	chr3:144969653-144969654	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs183189529	chr3:144969707-144969708	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs559854897	chr3:144969721-144969722	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs374555073	chr3:144969752-144969753	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs187936643	chr3:144969753-144969754	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs552020486	chr3:144969754-144969755	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs570230337	chr3:144969779-144969780	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs369247853	chr3:144969780-144969781	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs549387859	chr3:144969804-144969805	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs73016186	chr3:144969805-144969806	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs535073026	chr3:144969811-144969812	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs144801057	chr3:144969818-144969819	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs111726240	chr3:144969831-144969832	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs553512262	chr3:144969881-144969882	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs114691741	chr3:144969918-144969919	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs142800402	chr3:144969931-144969932	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs147443230	chr3:144969937-144969938	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs528278087	chr3:144969939-144969940	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Autism	18923514	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autism	21956041	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	16608533	CNVD
Schizophrenia	20967226	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:144965800-144970200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:144970200-144976200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:144976200-144976400	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr3:144976200-144977400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:144976200-144977600	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr3:144976400-144976600	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr3:144976400-144976800	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr3:144976400-144976800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
9	chr3:144976400-144977400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr3:144976400-144977400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr3:144976400-144977600	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr3:144976400-144977600	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr3:144976600-144977000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
14	chr3:144976600-144977400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr3:144976600-144977400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr3:144976600-144977400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr3:144976600-144977600	Enhancers	H1 Cell Line	embryonic stem cell
18	chr3:144976800-144977400	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr3:144977000-144977600	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr3:144977600-144978800	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr3:144990400-144990600	Enhancers	HSMM	muscle
22	chr3:145005000-145005200	Enhancers	GM12878-XiMat	blood
23	chr3:145021400-145021600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr3:145027200-145027600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr3:145031800-145032200	Enhancers	Fetal Kidney	kidney
26	chr3:145033000-145033800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr3:145033200-145033600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr3:145033200-145034800	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr3:145033400-145033800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr3:145033400-145034400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr3:145038800-145039200	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr3:145050400-145050800	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr3:145050600-145051000	Active TSS	ES-I3 Cell Line	embryonic stem cell
34	chr3:145050600-145051000	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr3:145051000-145052000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr3:145052000-145054800	Active TSS	ES-I3 Cell Line	embryonic stem cell
37	chr3:145054800-145070200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr3:145059600-145066000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr3:145066000-145066200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr3:145066000-145066200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr3:145066000-145066200	ZNF genes & repeats	Pancreas	Pancrea
42	chr3:145070200-145070600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
43	chr3:145070600-145071400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr3:145071400-145073000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
45	chr3:145074200-145076400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
46	chr3:145075000-145075600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
47	chr3:145075600-145076800	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr3:145076400-145084600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr3:145076800-145077200	Enhancers	H1 Cell Line	embryonic stem cell
50	chr3:145079600-145079800	Enhancers	Fetal Brain Male	brain

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