Variant report

Variant	nsv830140
Chromosome Location	chr4:165855999-165956612
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1640)
CpG islands
(count:2506)
Chromatin interactive
region (count:20)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1640 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:165938276-165938298	K562	blood:	n/a	n/a
2	ATF2	chr4:165877669-165878118	GM12878	blood:	n/a	n/a
3	ATF2	chr4:165930888-165931294	GM12878	blood:	n/a	n/a
4	ATF2	chr4:165898293-165899043	GM12878	blood:	n/a	n/a
5	BATF	chr4:165856995-165857356	GM12878	blood:	n/a	n/a
6	BATF	chr4:165857047-165857297	GM12878	blood:	n/a	n/a
7	BCL11A	chr4:165857038-165857347	GM12878	blood:	n/a	n/a
8	BCL11A	chr4:165856980-165857343	GM12878	blood:	n/a	n/a
9	BCLAF1	chr4:165898340-165899117	GM12878	blood:	n/a	chr4:165898823-165898832
10	BCLAF1	chr4:165877809-165878342	GM12878	blood:	n/a	n/a
11	BHLHE40	chr4:165880700-165880797	HepG2	liver:	n/a	n/a
12	BHLHE40	chr4:165927629-165927864	K562	blood:	n/a	n/a
13	BHLHE40	chr4:165877853-165878275	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:165898610-165899070	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:165857075-165857535	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:165877987-165878027	K562	blood:	n/a	n/a
17	BRCA1	chr4:165859210-165859241	GM12878	blood:	n/a	n/a
18	BRCA1	chr4:165898635-165898831	GM12878	blood:	n/a	n/a
19	CBX3	chr4:165877855-165878292	K562	blood:	n/a	n/a
20	CEBPB	chr4:165893196-165893391	K562	blood:	n/a	n/a
21	CEBPB	chr4:165918673-165918803	K562	blood:	n/a	n/a
22	CEBPB	chr4:165918720-165918746	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr4:165928087-165928406	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:165924291-165924463	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD1	chr4:165857436-165858121	GM12878	blood:	n/a	n/a
26	CHD1	chr4:165858664-165859460	GM12878	blood:	n/a	n/a
27	CHD2	chr4:165867270-165867286	GM12878	blood:	n/a	n/a
28	CHD2	chr4:165857085-165858018	GM12878	blood:	n/a	n/a
29	CHD2	chr4:165877922-165878553	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr4:165877860-165878562	GM12878	blood:	n/a	n/a
31	CHD2	chr4:165858814-165859380	GM12878	blood:	n/a	n/a
32	CHD2	chr4:165898446-165899204	GM12878	blood:	n/a	n/a
33	CREB1	chr4:165877796-165878486	GM12878	blood:	n/a	n/a
34	CREB1	chr4:165877817-165878316	A549	lung:	n/a	n/a
35	CREB1	chr4:165877895-165878381	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTBP2	chr4:165877837-165878615	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr4:165856640-165856790	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr4:165858802-165859034	LNCaP	prostate:	n/a	n/a
39	CTCF	chr4:165864520-165864670	MCF-7	breast:	n/a	n/a
40	CTCF	chr4:165870992-165871224	LNCaP	prostate:	n/a	n/a
41	CTCF	chr4:165870680-165870830	HMF	breast:	n/a	n/a
42	CTCF	chr4:165899100-165899250	GM12864	blood:	n/a	n/a
43	CTCF	chr4:165859081-165859373	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr4:165918548-165918816	ECC-1	luminal epithelium:	n/a	n/a
45	CTCF	chr4:165870640-165870790	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr4:165922720-165922870	HRE	kidney:	n/a	n/a
47	CTCF	chr4:165870720-165870870	HMEC	breast:	n/a	n/a
48	CTCF	chr4:165922700-165922850	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr4:165922700-165922850	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr4:165938180-165938330	NHEK	skin:	n/a	n/a

(count:2506 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:165898926-165898976	GM12891	blood:	n/a
2	chr4:165877875-165877925	AG09309	skin:	n/a
3	chr4:165954480-165954530	GM12878	blood:	n/a
4	chr4:165881424-165881474	ovcar-3	ovarian:	n/a
5	chr4:165898825-165898875	MCF10A-Er-Src	breast:	n/a
6	chr4:165898926-165898976	GM12891	blood:	n/a
7	chr4:165877875-165877925	AG09309	skin:	n/a
8	chr4:165954480-165954530	GM12878	blood:	n/a
9	chr4:165881424-165881474	ovcar-3	ovarian:	n/a
10	chr4:165898825-165898875	MCF10A-Er-Src	breast:	n/a
11	chr4:165953028-165953078	Jurkat	blood:	n/a
12	chr4:165878317-165878367	HRE	kidney:	n/a
13	chr4:165952731-165952781	NHDF-neo	bronchial:	n/a
14	chr4:165899396-165899446	HNPCEpiC	eye:	n/a
15	chr4:165953129-165953179	ovcar-3	ovarian:	n/a
16	chr4:165878317-165878367	NH-A	brain:	n/a
17	chr4:165952731-165952781	SKMC	muscle:	n/a
18	chr4:165898848-165898898	HCT-116	colon:	n/a
19	chr4:165928617-165928667	HNPCEpiC	eye:	n/a
20	chr4:165898835-165898885	SK-N-MC	brain:	n/a
21	chr4:165952835-165952885	SK-N-SH	brain:	n/a
22	chr4:165878091-165878141	PrEC	prostate:	n/a
23	chr4:165898666-165898716	GM12878	blood:	n/a
24	chr4:165898825-165898875	AoSMC	blood vessel:	n/a
25	chr4:165952835-165952885	HIPEpiC	eye:	n/a
26	chr4:165953207-165953257	HRCEpiC	kidney:	n/a
27	chr4:165954480-165954530	Jurkat	blood:	n/a
28	chr4:165898707-165898757	HMEC	breast:	n/a
29	chr4:165878055-165878105	Hepatocyte	liver:	n/a
30	chr4:165877045-165877095	SKMC	muscle:	n/a
31	chr4:165898912-165898962	HMEC	breast:	n/a
32	chr4:165898926-165898976	NB4	blood:	n/a
33	chr4:165898835-165898885	NH-A	brain:	n/a
34	chr4:165877045-165877095	AG10803	skin:	n/a
35	chr4:165953018-165953068	U87	brain:	n/a
36	chr4:165898825-165898875	HCPEpiC	choroid plexus:	n/a
37	chr4:165953018-165953068	Jurkat	blood:	n/a
38	chr4:165952839-165952889	AG04450	lung:	fetal
39	chr4:165941348-165941398	HRE	kidney:	n/a
40	chr4:165941348-165941398	AG04449	skin:	fetal
41	chr4:165953306-165953356	HMEC	breast:	n/a
42	chr4:165952839-165952889	HUVEC	blood vessel:	n/a
43	chr4:165878219-165878269	AG09319	gingival:	n/a
44	chr4:165900285-165900335	T-47D	breast:	n/a
45	chr4:165953131-165953181	AG10803	skin:	n/a
46	chr4:165878136-165878186	RPTEC	kidney:	n/a
47	chr4:165953207-165953257	MCF10A-Er-Src	breast:	n/a
48	chr4:165898848-165898898	NH-A	brain:	n/a
49	chr4:165953028-165953078	HCM	heart:	n/a
50	chr4:165898912-165898962	GM06990	blood:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:165868972..165872041-chr4:165876298..165879460,3	MCF-7	breast:
2	chr4:165874581..165877460-chr4:165878651..165880772,2	K562	blood:
3	chr4:165896605..165899172-chr4:165907116..165908745,2	MCF-7	breast:
4	chr4:165701014..165701543-chr4:165856051..165856573,2	MCF-7	breast:
5	chr4:165876835..165879626-chr4:165882281..165885476,4	MCF-7	breast:
6	chr4:165923507..165926386-chr4:165928187..165930464,2	K562	blood:
7	chr4:165877284..165881205-chr4:165885674..165889440,5	MCF-7	breast:
8	chr4:165689047..165689634-chr4:165918458..165919146,2	MCF-7	breast:
9	chr4:165874581..165877460-chr4:165878651..165880772,2	K562	blood:
10	chr1:11966992..11968590-chr4:165867023..165868624,2	K562	blood:
11	chr4:165876074..165878048-chr4:165892405..165894471,2	MCF-7	breast:
12	chr4:165866322..165867965-chr4:165877072..165879577,2	MCF-7	breast:
13	chr4:165896605..165899172-chr4:165907116..165908745,2	MCF-7	breast:
14	chr4:165868972..165872041-chr4:165876298..165879460,3	MCF-7	breast:
15	chr4:165876074..165878048-chr4:165892405..165894471,2	MCF-7	breast:
16	chr4:165868495..165870203-chr4:165872665..165874987,2	MCF-7	breast:
17	chr4:165699281..165700032-chr4:165856272..165857241,2	MCF-7	breast:
18	chr4:165918473..165921448-chr4:165932774..165935050,2	K562	blood:
19	chr4:165877542..165879531-chr4:165880684..165882237,2	MCF-7	breast:
20	chr4:165856166..165858715-chr4:165877906..165879898,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C4orf39-3	chr4:165882287-165882345	NONHSAT099093
2	lnc-C4orf39-3	chr4:165869231-165869699	NONHSAT099093
3	lnc-TRIM61-2	chr4:165856103-165856321	NONHSAT099091
4	lnc-TRIM61-1	chr4:165928238-165928367	XLOC_004145
5	lnc-C4orf39-5	chr4:165911021-165911093	l_2770_chr4:165894766-165911093_prostate
6	lnc-TRIM61-6	chr4:165933518-165933997	NONHSAT099100
7	lnc-C4orf39-4	chr4:165908417-165908939	NONHSAT099095
8	lnc-C4orf39-3	chr4:165883229-165883240	NONHSAT099093
9	lnc-C4orf39-5	chr4:165894767-165895013	l_2770_chr4:165894766-165911093_prostate
10	lnc-TRIM61-1	chr4:165928495-165929111	XLOC_004145
11	lnc-TMEM192-4	chr4:165889739-165891154	NONHSAT099094
12	lnc-C4orf39-3	chr4:165899902-165899980	NONHSAT099093

No data

Variant related genes	Relation type
ENSG00000250430	TF binding region
ENSG00000236941	TF binding region
ENSG00000270960	TF binding region
ENSG00000248229	TF binding region
ENSG00000250887	TF binding region
NACA3P	TF binding region
FAM218BP	TF binding region
ENSG00000248632	TF binding region
ENSG00000250712	TF binding region
TRIM60	TF binding region
FAM218A	TF binding region
TRIM61	TF binding region
ENSG00000248645	TF binding region
ENSG00000240674	TF binding region
ENSG00000250430	CpG island
ENSG00000236941	CpG island
ENSG00000270960	CpG island
ENSG00000248229	CpG island
ENSG00000250887	CpG island
NACA3P	CpG island
FAM218BP	CpG island
ENSG00000248632	CpG island
ENSG00000250712	CpG island
TRIM60	CpG island
FAM218A	CpG island
TRIM61	CpG island
ENSG00000248645	CpG island
ENSG00000240674	CpG island
ENSG00000248229	chromatin interactions
ENSG00000250486	chromatin interactions
ENSG00000250887	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000236941	chromatin interactions
ENSG00000183439	chromatin interactions
ENSG00000240674	chromatin interactions

Extended variants
information (count: 2891 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2891 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56653944	chr4:165856010-165856011	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs33977278	chr4:165856020-165856021	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs373428044	chr4:165856021-165856022	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs74771022	chr4:165856022-165856023	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs372243484	chr4:165856024-165856025	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs569282436	chr4:165856026-165856027	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs375277088	chr4:165856027-165856028	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs367898920	chr4:165856028-165856029	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs542953102	chr4:165856044-165856045	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs141590339	chr4:165856065-165856066	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs373685433	chr4:165856075-165856076	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs34063904	chr4:165856123-165856124	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs201531589	chr4:165856132-165856133	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs398064224	chr4:165856143-165856144	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs398108258	chr4:165856144-165856145	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs111578851	chr4:165856152-165856153	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs537891652	chr4:165856217-165856218	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs533052363	chr4:165856309-165856310	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs377442974	chr4:165856311-165856312	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs191950792	chr4:165856340-165856341	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs371850338	chr4:165856354-165856355	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs375062700	chr4:165856360-165856361	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs369090244	chr4:165856366-165856367	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs372449599	chr4:165856371-165856372	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs566552438	chr4:165856372-165856373	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs75526815	chr4:165856381-165856382	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs79175610	chr4:165856383-165856384	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs75330162	chr4:165856402-165856403	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs73871539	chr4:165856435-165856436	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs549024821	chr4:165856532-165856533	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs554943711	chr4:165856547-165856548	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs567206029	chr4:165856584-165856585	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs370376590	chr4:165856590-165856591	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs537875226	chr4:165856591-165856592	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs556134268	chr4:165856606-165856607	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs571446820	chr4:165856643-165856644	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs13140290	chr4:165856679-165856680	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs112563590	chr4:165856697-165856698	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs554188766	chr4:165856716-165856717	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs572572650	chr4:165856769-165856770	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs536819153	chr4:165856778-165856779	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs143655395	chr4:165856808-165856809	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs6848177	chr4:165856845-165856846	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs544268050	chr4:165856879-165856880	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs562479707	chr4:165856901-165856902	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs111434181	chr4:165856907-165856908	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs55676639	chr4:165856934-165856935	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs576994631	chr4:165856937-165856938	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs116211342	chr4:165856974-165856975	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs560159672	chr4:165856989-165856990	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Glioblastoma multiforme	22286061	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	16774939	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
intellectual deficit	22127048	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:861 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:165853400-165856800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:165853600-165857800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr4:165854200-165858600	Weak transcription	HSMMtube	muscle
4	chr4:165855200-165858800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:165855600-165856800	Enhancers	GM12878-XiMat	blood
6	chr4:165855800-165857200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr4:165856400-165856600	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr4:165856600-165858000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr4:165856800-165857000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr4:165856800-165857000	Flanking Active TSS	GM12878-XiMat	blood
11	chr4:165856800-165857600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr4:165857000-165857400	Enhancers	GM12878-XiMat	blood
13	chr4:165857000-165857800	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr4:165857200-165857600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr4:165857400-165859400	Flanking Active TSS	GM12878-XiMat	blood
16	chr4:165857600-165859200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr4:165857600-165859200	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr4:165857600-165859200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr4:165857600-165859200	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr4:165857800-165859200	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr4:165857800-165859200	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr4:165858000-165859200	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr4:165858600-165859000	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr4:165858600-165859000	Enhancers	Adipose Nuclei	Adipose
25	chr4:165858600-165859200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr4:165858600-165859200	Enhancers	HSMMtube	muscle
27	chr4:165858600-165859400	Enhancers	Fetal Muscle Leg	muscle
28	chr4:165858800-165859200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr4:165858800-165859200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr4:165858800-165859200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr4:165858800-165859200	Enhancers	Brain Substantia Nigra	brain
32	chr4:165858800-165859200	Enhancers	Fetal Lung	lung
33	chr4:165858800-165859200	Enhancers	Fetal Stomach	stomach
34	chr4:165859000-165860000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr4:165859200-165864400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr4:165859200-165869200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:165859400-165859600	Active TSS	GM12878-XiMat	blood
38	chr4:165859400-165861000	Weak transcription	Fetal Muscle Leg	muscle
39	chr4:165859600-165859800	Flanking Active TSS	GM12878-XiMat	blood
40	chr4:165859800-165860800	Weak transcription	GM12878-XiMat	blood
41	chr4:165860800-165861000	Enhancers	GM12878-XiMat	blood
42	chr4:165861200-165861400	Enhancers	Fetal Muscle Leg	muscle
43	chr4:165864200-165864600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr4:165864200-165864800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr4:165864400-165864600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr4:165864400-165864600	Bivalent Enhancer	Fetal Muscle Leg	muscle
47	chr4:165864400-165864800	Enhancers	NHEK	skin
48	chr4:165864600-165864800	Enhancers	Fetal Muscle Leg	muscle
49	chr4:165864600-165865000	Enhancers	HSMMtube	muscle
50	chr4:165864600-165865200	Enhancers	Placenta Amnion	Placenta Amnion

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