Variant report

Variant	nsv1035049
Chromosome Location	chr5:62027995-62875830
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2828)
CpG islands
(count:489)
Chromatin interactive
region (count:77)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2828 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:62037767-62038406	HepG2	liver:	n/a	n/a
2	ATF1	chr5:62351150-62351392	K562	blood:	n/a	n/a
3	ATF1	chr5:62269440-62269840	K562	blood:	n/a	n/a
4	ATF1	chr5:62345801-62346021	K562	blood:	n/a	n/a
5	ATF1	chr5:62341251-62341425	K562	blood:	n/a	n/a
6	ATF1	chr5:62556872-62557055	K562	blood:	n/a	n/a
7	ATF1	chr5:62427553-62427829	K562	blood:	n/a	n/a
8	ATF2	chr5:62697361-62697668	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr5:62719905-62719946	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr5:62701318-62701374	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr5:62397553-62397673	K562	blood:	n/a	n/a
12	BACH1	chr5:62747193-62747244	K562	blood:	n/a	n/a
13	BACH1	chr5:62619812-62620109	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr5:62265689-62265873	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr5:62753304-62753329	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL11A	chr5:62617005-62617179	GM12878	blood:	n/a	n/a
17	BCL3	chr5:62056284-62056836	GM12878	blood:	n/a	n/a
18	BCL3	chr5:62073699-62074050	GM12878	blood:	n/a	n/a
19	BHLHE40	chr5:62349021-62349249	HepG2	liver:	n/a	n/a
20	BHLHE40	chr5:62058497-62058551	GM12878	blood:	n/a	n/a
21	BHLHE40	chr5:62072439-62072720	K562	blood:	n/a	n/a
22	CBX3	chr5:62328196-62328627	K562	blood:	n/a	n/a
23	CBX3	chr5:62328193-62328706	K562	blood:	n/a	n/a
24	CEBPB	chr5:62497768-62497937	H1-hESC	embryonic stem cell:	n/a	chr5:62497872-62497885
25	CEBPB	chr5:62339627-62339962	IMR90	lung:	n/a	chr5:62339805-62339816 chr5:62339804-62339817
26	CEBPB	chr5:62337021-62337199	H1-hESC	embryonic stem cell:	n/a	chr5:62337042-62337053 chr5:62337041-62337054
27	CEBPB	chr5:62081416-62081734	K562	blood:	n/a	chr5:62081560-62081571
28	CEBPB	chr5:62183927-62184242	IMR90	lung:	n/a	chr5:62184085-62184096
29	CEBPB	chr5:62497466-62498123	MCF-7	breast:	n/a	chr5:62497872-62497885
30	CEBPB	chr5:62538821-62539063	A549	lung:	n/a	n/a
31	CEBPB	chr5:62251223-62251520	IMR90	lung:	n/a	chr5:62251358-62251369
32	CEBPB	chr5:62074801-62075107	Hela-S3	cervix:	n/a	chr5:62074994-62075011
33	CEBPB	chr5:62252491-62252751	HepG2	liver:	n/a	chr5:62252587-62252598 chr5:62252654-62252665
34	CEBPB	chr5:62445157-62445404	HepG2	liver:	n/a	n/a
35	CEBPB	chr5:62086167-62086547	HepG2	liver:	n/a	chr5:62086349-62086360
36	CEBPB	chr5:62336886-62337173	IMR90	lung:	n/a	chr5:62337042-62337053 chr5:62337041-62337054
37	CEBPB	chr5:62529760-62530021	IMR90	lung:	n/a	chr5:62529916-62529929 chr5:62529916-62529929 chr5:62529918-62529929 chr5:62529916-62529929
38	CEBPB	chr5:62529687-62530076	ECC-1	luminal epithelium:	n/a	chr5:62529916-62529929 chr5:62529916-62529929 chr5:62529918-62529929 chr5:62529916-62529929
39	CEBPB	chr5:62529590-62529982	H1-hESC	embryonic stem cell:	n/a	chr5:62529916-62529929 chr5:62529916-62529929 chr5:62529634-62529647 chr5:62529643-62529655 chr5:62529918-62529929 chr5:62529916-62529929
40	CEBPB	chr5:62257323-62257524	H1-hESC	embryonic stem cell:	n/a	chr5:62257416-62257427
41	CEBPB	chr5:62364471-62364554	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr5:62257238-62257586	A549	lung:	n/a	chr5:62257416-62257427
43	CEBPB	chr5:62610605-62610681	A549	lung:	n/a	n/a
44	CEBPB	chr5:62183940-62184226	A549	lung:	n/a	chr5:62184085-62184096
45	CEBPB	chr5:62659595-62659835	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr5:62086188-62086582	MCF-7	breast:	n/a	chr5:62086349-62086360
47	CEBPB	chr5:62529733-62530123	ECC-1	luminal epithelium:	n/a	chr5:62529916-62529929 chr5:62529916-62529929 chr5:62529918-62529929 chr5:62529916-62529929
48	CEBPB	chr5:62706384-62706626	IMR90	lung:	n/a	n/a
49	CEBPB	chr5:62327101-62327449	HepG2	liver:	n/a	chr5:62327257-62327270 chr5:62327267-62327280 chr5:62327258-62327269 chr5:62327257-62327270
50	CEBPB	chr5:62081409-62081741	HepG2	liver:	n/a	chr5:62081560-62081571

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:62073161-62073211	BJ	skin:	n/a
2	chr5:62073161-62073211	BJ	skin:	n/a
3	chr5:62071572-62071622	Caco-2	colon:	n/a
4	chr5:62071572-62071622	HEEpiC	esophagus:	n/a
5	chr5:62072660-62072710	SK-N-SH	brain:	n/a
6	chr5:62365115-62365165	HRPEpiC	eye:	n/a
7	chr5:62100540-62100590	SAEC	small airway:	n/a
8	chr5:62074572-62074622	HAEpiC	amniotic membrane:	n/a
9	chr5:62073623-62073673	HRPEpiC	eye:	n/a
10	chr5:62071572-62071622	MCF10A-Er-Src	breast:	n/a
11	chr5:62074261-62074311	AG10803	skin:	n/a
12	chr5:62071572-62071622	HCF	heart:	n/a
13	chr5:62073623-62073673	HAEpiC	amniotic membrane:	n/a
14	chr5:62100540-62100590	PFSK-1	brain:	n/a
15	chr5:62071572-62071622	AG09319	gingival:	n/a
16	chr5:62074261-62074311	AoSMC	blood vessel:	n/a
17	chr5:62365115-62365165	NHDF-neo	bronchial:	n/a
18	chr5:62074572-62074622	SK-N-SH	brain:	n/a
19	chr5:62072660-62072710	RPTEC	kidney:	n/a
20	chr5:62073623-62073673	GM12892	blood:	n/a
21	chr5:62074572-62074622	PrEC	prostate:	n/a
22	chr5:62074572-62074622	IMR90	lung:	fetal
23	chr5:62074261-62074311	PFSK-1	brain:	n/a
24	chr5:62072660-62072710	NH-A	brain:	n/a
25	chr5:62365115-62365165	A549	lung:	n/a
26	chr5:62073161-62073211	HPAEpiC	pulmonary alveolar:	n/a
27	chr5:62072660-62072710	Jurkat	blood:	n/a
28	chr5:62071572-62071622	GM12878	blood:	n/a
29	chr5:62074261-62074311	BE2_C	brain:	n/a
30	chr5:62071572-62071622	PFSK-1	brain:	n/a
31	chr5:62073623-62073673	HL-60	blood:	n/a
32	chr5:62074572-62074622	HNPCEpiC	eye:	n/a
33	chr5:62100540-62100590	K562	blood:	n/a
34	chr5:62100540-62100590	RPTEC	kidney:	n/a
35	chr5:62073161-62073211	SK-N-MC	brain:	n/a
36	chr5:62100540-62100590	Caco-2	colon:	n/a
37	chr5:62074572-62074622	HEEpiC	esophagus:	n/a
38	chr5:62074572-62074622	HCPEpiC	choroid plexus:	n/a
39	chr5:62071572-62071622	SAEC	small airway:	n/a
40	chr5:62071572-62071622	H1-hESC	embryonic stem cell:	embryo
41	chr5:62074261-62074311	AG04449	skin:	fetal
42	chr5:62074572-62074622	HepG2	liver:	n/a
43	chr5:62100540-62100590	HNPCEpiC	eye:	n/a
44	chr5:62073161-62073211	NB4	blood:	n/a
45	chr5:62074572-62074622	GM06990	blood:	n/a
46	chr5:62365115-62365165	AG04449	skin:	fetal
47	chr5:62100540-62100590	HRE	kidney:	n/a
48	chr5:62100540-62100590	U87	brain:	n/a
49	chr5:62071572-62071622	SK-N-MC	brain:	n/a
50	chr5:62072660-62072710	CMK	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:62036443..62039207-chr5:62041195..62044511,3	K562	blood:
2	chr5:62688331..62691927-chr5:62694917..62699039,4	K562	blood:
3	chr5:62272651..62274296-chr5:62275917..62277467,2	K562	blood:
4	chr5:62061013..62063521-chr5:62063661..62066191,2	K562	blood:
5	chr17:56736164..56737083-chr5:62632172..62633192,29	MCF-7	breast:
6	chr5:62542467..62544427-chr5:62546236..62548997,2	K562	blood:
7	chr17:56735268..56738937-chr5:62632672..62634192,8	MCF-7	breast:
8	chr5:62542753..62544427-chr5:62547442..62548997,2	K562	blood:
9	chr5:62412476..62414687-chr5:62419094..62420921,2	K562	blood:
10	chr5:62689129..62691869-chr5:62694201..62697545,3	K562	blood:
11	chr2:239891948..239892626-chr5:62328345..62328845,2	K562	blood:
12	chr17:56736170..56736865-chr5:62632672..62633192,4	Hela-S3	cervix:
13	chr5:62069461..62071077-chr5:62076501..62078748,2	K562	blood:
14	chr5:62078011..62080327-chr5:62081236..62083654,2	K562	blood:
15	chr5:62730491..62733268-chr5:62735229..62737200,2	K562	blood:
16	chr5:62030684..62032945-chr5:62039649..62042488,2	MCF-7	breast:
17	chr5:62412476..62414687-chr5:62419094..62420921,2	K562	blood:
18	chr5:62421535..62422320-chr5:62693970..62694916,3	MCF-7	breast:
19	chr5:61756022..61757748-chr5:62074424..62075807,9	MCF-7	breast:
20	chr5:62421535..62422320-chr5:62693970..62694916,3	MCF-7	breast:
21	chr5:62535956..62538795-chr5:62539410..62541239,2	K562	blood:
22	chr5:62729811..62731369-chr5:62732550..62734446,2	MCF-7	breast:
23	chr5:62689129..62691869-chr5:62694201..62697545,3	K562	blood:
24	chr5:62193925..62195577-chr5:62201485..62203661,2	MCF-7	breast:
25	chr5:62606697..62608384-chr5:62610156..62611740,2	MCF-7	breast:
26	chr5:62542753..62544427-chr5:62547442..62548997,2	K562	blood:
27	chr5:62078011..62080327-chr5:62081236..62083654,2	K562	blood:
28	chr5:62688331..62691927-chr5:62694917..62699039,4	K562	blood:
29	chr5:62582710..62584559-chr5:62585298..62587676,2	MCF-7	breast:
30	chr5:62036443..62039207-chr5:62041195..62044511,3	K562	blood:
31	chr5:62177885..62179876-chr5:62180704..62182544,2	K562	blood:
32	chr5:61756416..61757318-chr5:62074341..62075268,4	K562	blood:
33	chr5:62535956..62538795-chr5:62539410..62541239,2	K562	blood:
34	chr5:62697016..62697521-chr5:63907910..63908892,2	K562	blood:
35	chr5:62697027..62697873-chr5:63395970..63396618,2	MCF-7	breast:
36	chr5:62744743..62747073-chr5:62749692..62752090,2	K562	blood:
37	chr5:62080331..62084292-chr5:62086443..62088883,3	K562	blood:
38	chr5:62349615..62352403-chr5:62352864..62355347,2	MCF-7	breast:
39	chr5:62503002..62504895-chr5:62506873..62508754,2	MCF-7	breast:
40	chr5:62697415..62698450-chr5:62724267..62725316,3	MCF-7	breast:
41	chr5:62681299..62684293-chr5:62685563..62687672,2	K562	blood:
42	chr5:62272651..62274296-chr5:62275917..62277467,2	K562	blood:
43	chr5:62068406..62072262-chr5:62073628..62078748,5	K562	blood:
44	chr5:62080331..62084292-chr5:62086443..62088883,3	K562	blood:
45	chr17:56736265..56737048-chr5:62632672..62633192,2	MCF-7	breast:
46	chr5:62071591..62073108-chr5:62074194..62077077,2	K562	blood:
47	chr5:62017098..62019061-chr5:62042354..62044460,2	K562	blood:
48	chr5:5008094..5008743-chr5:62214886..62215776,2	K562	blood:
49	chr5:62681299..62684293-chr5:62685563..62687672,2	K562	blood:
50	chr5:62729811..62731369-chr5:62732550..62734446,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DIMT1-5	chr5:62318746-62319316	NONHSAT101720

No data

Variant related genes	Relation type
ISCA1P1	TF binding region
ENSG00000248185	TF binding region
ENSG00000249579	TF binding region
ISCA1P1	CpG island
ENSG00000248185	CpG island
ENSG00000249579	CpG island
ENSG00000202077	chromatin interactions
ENSG00000217416	chromatin interactions

Extended variants
information (count: 11206 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:11206 , 50 per page) page: 1 2 3 4 5 6 7 ... 225

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150650661	chr5:62028056-62028057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs192552454	chr5:62028101-62028102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561863707	chr5:62028102-62028103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs139755206	chr5:62028127-62028128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530375121	chr5:62028149-62028150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185613065	chr5:62028203-62028204	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs529520161	chr5:62028210-62028211	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs554869367	chr5:62028241-62028242	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs574622888	chr5:62028297-62028298	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs543636482	chr5:62028328-62028329	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs143667401	chr5:62028516-62028517	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs532292499	chr5:62028569-62028570	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs545917844	chr5:62028622-62028623	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs559452237	chr5:62028660-62028661	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs567232818	chr5:62028667-62028668	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs190519482	chr5:62028670-62028671	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs181840629	chr5:62028690-62028691	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs568766807	chr5:62028696-62028697	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs146307557	chr5:62028715-62028716	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs139472582	chr5:62028722-62028723	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs558909922	chr5:62028782-62028783	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs549875599	chr5:62028802-62028803	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs570711455	chr5:62028810-62028811	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs533075746	chr5:62028811-62028812	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs539601293	chr5:62028845-62028846	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs251171	chr5:62028878-62028879	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs566597681	chr5:62028934-62028935	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs184460498	chr5:62028935-62028936	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs555460110	chr5:62028948-62028949	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs188826224	chr5:62028986-62028987	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs543349686	chr5:62028996-62028997	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs557246953	chr5:62029005-62029006	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs28630457	chr5:62029017-62029018	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs577121499	chr5:62029071-62029072	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs181260588	chr5:62029136-62029137	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs116808695	chr5:62029149-62029150	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs185510877	chr5:62029227-62029228	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs142604067	chr5:62029261-62029262	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs541847320	chr5:62029265-62029266	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs561521060	chr5:62029269-62029270	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs530476028	chr5:62029307-62029308	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs251172	chr5:62029339-62029340	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs564402685	chr5:62029351-62029352	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs533369388	chr5:62029381-62029382	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs546767862	chr5:62029396-62029397	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs189916739	chr5:62029479-62029480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs535300116	chr5:62029481-62029482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs368059972	chr5:62029519-62029520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs370743300	chr5:62029520-62029521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs180780119	chr5:62029545-62029546	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	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
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	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
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
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:782 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:62026400-62029800	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr5:62026800-62028400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr5:62027600-62028200	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr5:62028200-62029400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:62028200-62029400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
6	chr5:62028400-62029000	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr5:62029400-62029600	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr5:62032000-62032600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr5:62033200-62033600	Enhancers	Ovary	ovary
10	chr5:62033600-62039400	Weak transcription	Ovary	ovary
11	chr5:62037200-62037800	Enhancers	Fetal Intestine Large	intestine
12	chr5:62037200-62037800	Enhancers	HepG2	liver
13	chr5:62037200-62040000	Enhancers	Fetal Intestine Small	intestine
14	chr5:62037600-62039200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr5:62037800-62038000	Flanking Active TSS	HepG2	liver
16	chr5:62037800-62038200	Weak transcription	Fetal Intestine Large	intestine
17	chr5:62038000-62038200	Enhancers	HepG2	liver
18	chr5:62038200-62038400	Flanking Active TSS	HepG2	liver
19	chr5:62038200-62039200	Enhancers	Brain Germinal Matrix	brain
20	chr5:62038200-62040200	Enhancers	Fetal Intestine Large	intestine
21	chr5:62038400-62039400	Enhancers	A549	lung
22	chr5:62038400-62040400	Enhancers	HepG2	liver
23	chr5:62038600-62039000	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr5:62039200-62039600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr5:62039200-62039600	Weak transcription	Brain Germinal Matrix	brain
26	chr5:62039400-62039800	Enhancers	Ovary	ovary
27	chr5:62039400-62040200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr5:62039600-62040000	Enhancers	Brain Germinal Matrix	brain
29	chr5:62039600-62040400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr5:62040000-62040400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr5:62040200-62045200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr5:62045200-62045600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr5:62048000-62048600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
34	chr5:62048000-62049200	Active TSS	A549	lung
35	chr5:62048000-62049200	Active TSS	Hela-S3	cervix
36	chr5:62048200-62049000	Active TSS	K562	blood
37	chr5:62048600-62049000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr5:62066600-62067600	Enhancers	Fetal Kidney	kidney
39	chr5:62073800-62074000	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr5:62073800-62074600	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr5:62074000-62074200	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr5:62074000-62074600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr5:62074000-62075000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
44	chr5:62074000-62075400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr5:62074200-62074600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr5:62074200-62074800	Enhancers	Fetal Lung	lung
47	chr5:62074200-62075000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
48	chr5:62074200-62075000	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr5:62074400-62074600	Enhancers	Primary hematopoietic stem cells	blood
50	chr5:62074400-62075000	Enhancers	Primary B cells from cord blood	blood

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