Variant report

Variant	nsv882192
Chromosome Location	chr5:74641707-74707762
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:743)
CpG islands
(count:305)
Chromatin interactive
region (count:25)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:743 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:74669706-74670670	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:74701386-74701433	K562	blood:	n/a	n/a
3	ARID3A	chr5:74677285-74677772	K562	blood:	n/a	chr5:74677737-74677753
4	ATF1	chr5:74677187-74677677	K562	blood:	n/a	n/a
5	ATF2	chr5:74662613-74663071	GM12878	blood:	n/a	n/a
6	BATF	chr5:74662605-74663017	GM12878	blood:	n/a	n/a
7	BCL3	chr5:74662608-74663015	GM12878	blood:	n/a	n/a
8	BCLAF1	chr5:74662614-74663129	GM12878	blood:	n/a	n/a
9	BHLHE40	chr5:74658467-74658585	K562	blood:	n/a	n/a
10	BHLHE40	chr5:74660416-74660490	GM12878	blood:	n/a	n/a
11	BHLHE40	chr5:74662691-74663156	GM12878	blood:	n/a	n/a
12	BHLHE40	chr5:74669765-74670604	HepG2	liver:	n/a	n/a
13	BHLHE40	chr5:74670189-74670530	HepG2	liver:	n/a	n/a
14	BHLHE40	chr5:74677408-74677666	K562	blood:	n/a	n/a
15	BHLHE40	chr5:74670215-74670528	HepG2	liver:	n/a	n/a
16	CBX3	chr5:74700977-74701627	HCT-116	colon:	n/a	n/a
17	CCNT2	chr5:74658916-74659778	K562	blood:	n/a	n/a
18	CCNT2	chr5:74677360-74677651	K562	blood:	n/a	n/a
19	CCNT2	chr5:74660194-74660456	K562	blood:	n/a	n/a
20	CEBPB	chr5:74685227-74685426	K562	blood:	n/a	chr5:74685264-74685275 chr5:74685380-74685397 chr5:74685266-74685277
21	CEBPB	chr5:74660764-74661019	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr5:74670284-74670592	HepG2	liver:	n/a	chr5:74670514-74670525
23	CEBPB	chr5:74669699-74670068	HepG2	liver:	n/a	n/a
24	CEBPB	chr5:74662339-74662672	HepG2	liver:	n/a	n/a
25	CEBPB	chr5:74660810-74661019	A549	lung:	n/a	n/a
26	CEBPB	chr5:74670504-74670541	K562	blood:	n/a	chr5:74670514-74670525
27	CEBPB	chr5:74658913-74659293	HepG2	liver:	n/a	n/a
28	CEBPB	chr5:74670343-74670685	HepG2	liver:	n/a	chr5:74670514-74670525
29	CEBPB	chr5:74685294-74685316	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr5:74660774-74661012	HepG2	liver:	n/a	n/a
31	CEBPB	chr5:74662309-74662646	K562	blood:	n/a	n/a
32	CEBPB	chr5:74670274-74670718	HepG2	liver:	n/a	chr5:74670514-74670525
33	CEBPB	chr5:74685154-74685390	HepG2	liver:	n/a	chr5:74685264-74685275 chr5:74685266-74685277
34	CEBPB	chr5:74659217-74659319	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr5:74670404-74670578	HepG2	liver:	n/a	chr5:74670514-74670525
36	CEBPB	chr5:74660765-74661033	K562	blood:	n/a	n/a
37	CEBPB	chr5:74660777-74661036	IMR90	lung:	n/a	n/a
38	CEBPB	chr5:74662477-74662531	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPD	chr5:74677240-74677655	K562	blood:	n/a	n/a
40	CEBPD	chr5:74677221-74677746	K562	blood:	n/a	n/a
41	CHD2	chr5:74662850-74663095	GM12878	blood:	n/a	n/a
42	CHD2	chr5:74660499-74660695	HepG2	liver:	n/a	n/a
43	CHD2	chr5:74658421-74658614	K562	blood:	n/a	n/a
44	CHD2	chr5:74659479-74659913	K562	blood:	n/a	n/a
45	CTCF	chr5:74664280-74664430	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr5:74648184-74648227	ProgFib	skin:	n/a	n/a
47	CTCF	chr5:74664240-74664390	GM12864	blood:	n/a	n/a
48	CTCF	chr5:74670635-74670695	LNCaP	prostate:	n/a	n/a
49	CUX1	chr5:74677411-74677902	K562	blood:	n/a	n/a
50	CUX1	chr5:74661308-74661604	K562	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:74657448-74657498	HCPEpiC	choroid plexus:	n/a
2	chr5:74707372-74707422	HepG2	liver:	n/a
3	chr5:74641899-74641949	Hepatocyte	liver:	n/a
4	chr5:74707372-74707422	ProgFib	skin:	n/a
5	chr5:74707372-74707422	NT2-D1	testis:	n/a
6	chr5:74641899-74641949	ProgFib	skin:	n/a
7	chr5:74707372-74707422	PANC-1	pancreas:	n/a
8	chr5:74641899-74641949	NB4	blood:	n/a
9	chr5:74659162-74659212	A549	lung:	n/a
10	chr5:74672346-74672396	HepG2	liver:	n/a
11	chr5:74659162-74659212	T-47D	breast:	n/a
12	chr5:74659162-74659212	NH-A	brain:	n/a
13	chr5:74641899-74641949	NHDF-neo	bronchial:	n/a
14	chr5:74641899-74641949	HCT-116	colon:	n/a
15	chr5:74659162-74659212	HRE	kidney:	n/a
16	chr5:74672346-74672396	NHBE	bronchial:	n/a
17	chr5:74657448-74657498	HRE	kidney:	n/a
18	chr5:74707372-74707422	HIPEpiC	eye:	n/a
19	chr5:74657448-74657498	GM12891	blood:	n/a
20	chr5:74659162-74659212	PrEC	prostate:	n/a
21	chr5:74657448-74657498	PANC-1	pancreas:	n/a
22	chr5:74707372-74707422	HCF	heart:	n/a
23	chr5:74657448-74657498	ECC-1	luminal epithelium:	n/a
24	chr5:74659162-74659212	HCF	heart:	n/a
25	chr5:74657448-74657498	AG09309	skin:	n/a
26	chr5:74641899-74641949	GM12891	blood:	n/a
27	chr5:74659162-74659212	ECC-1	luminal epithelium:	n/a
28	chr5:74672346-74672396	HAEpiC	amniotic membrane:	n/a
29	chr5:74659162-74659212	HAEpiC	amniotic membrane:	n/a
30	chr5:74659162-74659212	K562	blood:	n/a
31	chr5:74672346-74672396	Hela-S3	cervix:	n/a
32	chr5:74657448-74657498	NHDF-neo	bronchial:	n/a
33	chr5:74657448-74657498	NH-A	brain:	n/a
34	chr5:74672346-74672396	GM12892	blood:	n/a
35	chr5:74707372-74707422	HAEpiC	amniotic membrane:	n/a
36	chr5:74659162-74659212	AG09309	skin:	n/a
37	chr5:74657448-74657498	NB4	blood:	n/a
38	chr5:74672346-74672396	ProgFib	skin:	n/a
39	chr5:74657448-74657498	AG10803	skin:	n/a
40	chr5:74641899-74641949	NHBE	bronchial:	n/a
41	chr5:74659162-74659212	CMK	blood:	n/a
42	chr5:74672346-74672396	HRE	kidney:	n/a
43	chr5:74641899-74641949	AG04450	lung:	fetal
44	chr5:74672346-74672396	SK-N-MC	brain:	n/a
45	chr5:74672346-74672396	U87	brain:	n/a
46	chr5:74707372-74707422	CMK	blood:	n/a
47	chr5:74657448-74657498	SK-N-SH_RA	brain:	n/a
48	chr5:74641899-74641949	AG09319	gingival:	n/a
49	chr5:74707372-74707422	HEK293	kidney:	embryo
50	chr5:74707372-74707422	MCF-7	breast:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:74656438..74658329-chr5:74806583..74808480,2	MCF-7	breast:
2	chr5:74649780..74652799-chr5:74656910..74662122,4	K562	blood:
3	chr5:74649780..74652799-chr5:74656910..74662122,4	K562	blood:
4	chr5:74645396..74648342-chr5:74649968..74653709,3	K562	blood:
5	chr5:74653801..74656731-chr5:74656826..74658385,2	K562	blood:
6	chr5:74645396..74648342-chr5:74649968..74653709,3	K562	blood:
7	chr5:74635121..74639261-chr5:74640942..74643106,3	MCF-7	breast:
8	chr5:74695714..74697821-chr5:74698263..74700254,2	K562	blood:
9	chr5:74674905..74677858-chr5:74706669..74708493,2	K562	blood:
10	chr5:74653986..74657111-chr5:74658520..74660531,3	K562	blood:
11	chr5:74631027..74633689-chr5:74669899..74673257,3	MCF-7	breast:
12	chr5:74632494..74633998-chr5:74680778..74683249,2	MCF-7	breast:
13	chr5:74630501..74635424-chr5:74638636..74642776,5	K562	blood:
14	chr5:74653986..74657111-chr5:74658520..74660531,3	K562	blood:
15	chr5:74704826..74707671-chr5:74805831..74807766,2	MCF-7	breast:
16	chr5:74688554..74690802-chr5:74806794..74808772,2	MCF-7	breast:
17	chr5:74632373..74634214-chr5:74651079..74652927,2	MCF-7	breast:
18	chr13:91669308..91669910-chr5:74664857..74665857,2	K562	blood:
19	chr5:74662824..74664382-chr5:74665830..74667835,2	K562	blood:
20	chr5:74634550..74639803-chr5:74643156..74647439,6	MCF-7	breast:
21	chr5:74635076..74636775-chr5:74642889..74645067,2	K562	blood:
22	chr5:74638395..74641765-chr5:74658081..74661333,3	K562	blood:
23	chr5:74674905..74677858-chr5:74706669..74708493,2	K562	blood:
24	chr5:74641032..74643144-chr5:74649834..74652816,2	MCF-7	breast:
25	chr5:74650951..74652799-chr5:74656910..74659506,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HMGCR-2	chr5:74670288-74670634	NONHSAT102207
2	lnc-HMGCR-1	chr5:74659585-74660067	ENSG00000271815.1
3	lnc-ANKRD31-2	chr5:74664312-74667666	NONHSAT102205

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	HMGCR	hsa-miR-32-5p	chr5:74656500-74656523
2	HMGCR	hsa-miR-335-5p	chr5:74657557-74657580
3	HMGCR	hsa-miR-29c-3p	chr5:74656684-74656690
4	HMGCR	hsa-miR-29c-3p	chr5:74656670-74656691
5	HMGCR	hsa-miR-92a-3p	chr5:74656502-74656523

Variant related genes	Relation type
ENSG00000242198	TF binding region
HMGCR	TF binding region
COL4A3BP	TF binding region
ENSG00000271815	TF binding region
ENSG00000242198	CpG island
HMGCR	CpG island
COL4A3BP	CpG island
ENSG00000271815	CpG island
ENSG00000122008	chromatin interactions
ENSG00000113163	chromatin interactions
ENSG00000271815	chromatin interactions
ENSG00000113161	chromatin interactions
ENSG00000247372	chromatin interactions

Extended variants
information (count: 2433 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2433 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2303152	chr5:74641707-74641708	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs192575760	chr5:74641711-74641712	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs553983499	chr5:74641747-74641748	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs570548263	chr5:74641748-74641749	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs545274060	chr5:74641783-74641784	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs185701416	chr5:74641809-74641810	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs17238435	chr5:74641826-74641827	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs575268981	chr5:74641836-74641837	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs189377188	chr5:74641919-74641920	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs576048578	chr5:74641953-74641954	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs541785571	chr5:74642031-74642032	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs555323579	chr5:74642086-74642087	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs192517674	chr5:74642091-74642092	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs541162825	chr5:74642135-74642136	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs17238442	chr5:74642185-74642186	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs527991243	chr5:74642195-74642196	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs533322569	chr5:74642204-74642205	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs372729715	chr5:74642208-74642209	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs78078959	chr5:74642305-74642306	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs17238449	chr5:74642408-74642409	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs17244827	chr5:74642432-74642433	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs188717128	chr5:74642556-74642557	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs181447693	chr5:74642599-74642600	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs570060133	chr5:74642616-74642617	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs530386154	chr5:74642751-74642752	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs186179713	chr5:74642767-74642768	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs547137569	chr5:74642835-74642836	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs71600457	chr5:74642837-74642838	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs17244834	chr5:74642848-74642849	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs17244841	chr5:74642855-74642856	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs556435401	chr5:74642873-74642874	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs560735705	chr5:74642919-74642920	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs569645929	chr5:74642939-74642940	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs139090156	chr5:74642950-74642951	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs368129510	chr5:74643053-74643054	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs139887868	chr5:74643054-74643055	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs528117857	chr5:74643104-74643105	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs200573753	chr5:74643175-74643176	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs189329353	chr5:74643299-74643300	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs543289395	chr5:74643304-74643305	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs149888475	chr5:74643359-74643360	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs200347465	chr5:74643397-74643398	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs557917567	chr5:74643449-74643450	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs146417659	chr5:74643450-74643451	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs182319457	chr5:74643478-74643479	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs543690350	chr5:74643479-74643480	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs544969270	chr5:74643522-74643523	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs563851464	chr5:74643578-74643579	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs529662049	chr5:74643582-74643583	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs17244848	chr5:74643670-74643671	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	22355333	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Obesity	20935630	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:1604 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74633800-74645800	Weak transcription	Gastric	stomach
2	chr5:74633800-74645800	Weak transcription	Spleen	Spleen
3	chr5:74633800-74650400	Weak transcription	Pancreas	Pancrea
4	chr5:74634400-74645400	Weak transcription	Psoas Muscle	Psoas
5	chr5:74634400-74645600	Weak transcription	Esophagus	oesophagus
6	chr5:74634400-74650800	Weak transcription	Aorta	Aorta
7	chr5:74634400-74652400	Weak transcription	Right Ventricle	heart
8	chr5:74634600-74642200	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr5:74634600-74644200	Weak transcription	Rectal Smooth Muscle	rectum
10	chr5:74634800-74641800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr5:74635000-74641800	Weak transcription	Primary hematopoietic stem cells	blood
12	chr5:74635000-74643000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr5:74635000-74644200	Weak transcription	Brain Angular Gyrus	brain
14	chr5:74635000-74645200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr5:74635000-74652600	Weak transcription	Fetal Heart	heart
16	chr5:74635600-74659600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr5:74635800-74641800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr5:74635800-74641800	Weak transcription	Fetal Lung	lung
19	chr5:74635800-74644400	Weak transcription	Ovary	ovary
20	chr5:74635800-74645400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr5:74635800-74646000	Weak transcription	Small Intestine	intestine
22	chr5:74636400-74643400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr5:74636400-74645400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr5:74636800-74641800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr5:74636800-74645800	Weak transcription	Stomach Mucosa	stomach
26	chr5:74636800-74649200	Strong transcription	K562	blood
27	chr5:74636800-74659200	Strong transcription	HUES48 Cell Line	embryonic stem cell
28	chr5:74637200-74655800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr5:74637200-74659600	Strong transcription	HUES64 Cell Line	embryonic stem cell
30	chr5:74637800-74658400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
31	chr5:74637800-74658800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr5:74638000-74642400	Weak transcription	Fetal Kidney	kidney
33	chr5:74638000-74643000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr5:74638200-74658400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
35	chr5:74638200-74659800	Strong transcription	Monocytes-CD14+_RO01746	blood
36	chr5:74638200-74660400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
37	chr5:74638200-74660400	Strong transcription	Fetal Thymus	thymus
38	chr5:74638400-74642800	Strong transcription	Fetal Stomach	stomach
39	chr5:74638400-74657600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr5:74638400-74657800	Strong transcription	H9 Cell Line	embryonic stem cell
41	chr5:74638400-74659000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr5:74638400-74659000	Strong transcription	Primary monocytes fromperipheralblood	blood
43	chr5:74638400-74659000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr5:74638400-74659200	Strong transcription	Primary T helper cells fromperipheralblood	blood
45	chr5:74638400-74659200	Strong transcription	Duodenum Mucosa	Duodenum
46	chr5:74638400-74659800	Strong transcription	Primary neutrophils fromperipheralblood	blood
47	chr5:74638600-74655000	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr5:74638600-74659200	Strong transcription	Dnd41	blood
49	chr5:74638600-74659400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr5:74638600-74659600	Strong transcription	HUES6 Cell Line	embryonic stem cell

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