Variant report

Variant	nsv1022825
Chromosome Location	chr5:62025524-62874332
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2828)
CpG islands
(count:488)
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	chr5:62556872-62557055	K562	blood:	n/a	n/a
3	ATF1	chr5:62341251-62341425	K562	blood:	n/a	n/a
4	ATF1	chr5:62269440-62269840	K562	blood:	n/a	n/a
5	ATF1	chr5:62345801-62346021	K562	blood:	n/a	n/a
6	ATF1	chr5:62427553-62427829	K562	blood:	n/a	n/a
7	ATF1	chr5:62351150-62351392	K562	blood:	n/a	n/a
8	ATF2	chr5:62697361-62697668	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr5:62265689-62265873	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr5:62619812-62620109	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr5:62701318-62701374	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr5:62753304-62753329	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr5:62747193-62747244	K562	blood:	n/a	n/a
14	BACH1	chr5:62719905-62719946	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr5:62397553-62397673	K562	blood:	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	chr5:62257323-62257524	H1-hESC	embryonic stem cell:	n/a	chr5:62257416-62257427
25	CEBPB	chr5:62706384-62706626	IMR90	lung:	n/a	n/a
26	CEBPB	chr5:62539757-62540049	MCF-7	breast:	n/a	chr5:62539843-62539854
27	CEBPB	chr5:62529687-62530076	ECC-1	luminal epithelium:	n/a	chr5:62529916-62529929 chr5:62529916-62529929 chr5:62529918-62529929 chr5:62529916-62529929
28	CEBPB	chr5:62339657-62339970	Hela-S3	cervix:	n/a	chr5:62339805-62339816 chr5:62339804-62339817
29	CEBPB	chr5:62538821-62539063	A549	lung:	n/a	n/a
30	CEBPB	chr5:62551363-62551933	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr5:62074801-62075107	Hela-S3	cervix:	n/a	chr5:62074994-62075011
32	CEBPB	chr5:62086172-62086415	HepG2	liver:	n/a	chr5:62086349-62086360
33	CEBPB	chr5:62081416-62081734	K562	blood:	n/a	chr5:62081560-62081571
34	CEBPB	chr5:62069362-62069624	IMR90	lung:	n/a	chr5:62069514-62069525
35	CEBPB	chr5:62339713-62339874	K562	blood:	n/a	chr5:62339805-62339816 chr5:62339804-62339817
36	CEBPB	chr5:62150427-62150673	IMR90	lung:	n/a	n/a
37	CEBPB	chr5:62236464-62236527	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr5:62086187-62086537	HepG2	liver:	n/a	chr5:62086349-62086360
39	CEBPB	chr5:62697038-62697460	HepG2	liver:	n/a	chr5:62697274-62697287 chr5:62697274-62697285
40	CEBPB	chr5:62476932-62476970	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr5:62327101-62327449	HepG2	liver:	n/a	chr5:62327257-62327270 chr5:62327267-62327280 chr5:62327258-62327269 chr5:62327257-62327270
42	CEBPB	chr5:62497557-62498094	MCF-7	breast:	n/a	chr5:62497872-62497885
43	CEBPB	chr5:62086188-62086582	MCF-7	breast:	n/a	chr5:62086349-62086360
44	CEBPB	chr5:62183934-62184264	HepG2	liver:	n/a	chr5:62184085-62184096
45	CEBPB	chr5:62327108-62327452	A549	lung:	n/a	chr5:62327257-62327270 chr5:62327267-62327280 chr5:62327258-62327269 chr5:62327257-62327270
46	CEBPB	chr5:62654318-62654599	K562	blood:	n/a	chr5:62654447-62654458
47	CEBPB	chr5:62081409-62081741	HepG2	liver:	n/a	chr5:62081560-62081571
48	CEBPB	chr5:62336886-62337173	IMR90	lung:	n/a	chr5:62337042-62337053 chr5:62337041-62337054
49	CEBPB	chr5:62336913-62337189	HepG2	liver:	n/a	chr5:62337042-62337053 chr5:62337041-62337054
50	CEBPB	chr5:62689136-62689412	H1-hESC	embryonic stem cell:	n/a	chr5:62689260-62689271

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:62073623-62073673	PFSK-1	brain:	n/a
2	chr5:62073161-62073211	HUVEC	blood vessel:	n/a
3	chr5:62074572-62074622	GM12891	blood:	n/a
4	chr5:62073161-62073211	AG09309	skin:	n/a
5	chr5:62072660-62072710	ECC-1	luminal epithelium:	n/a
6	chr5:62365115-62365165	A549	lung:	n/a
7	chr5:62074261-62074311	HAEpiC	amniotic membrane:	n/a
8	chr5:62365115-62365165	HMEC	breast:	n/a
9	chr5:62071572-62071622	MCF-7	breast:	n/a
10	chr5:62073161-62073211	NHDF-neo	bronchial:	n/a
11	chr5:62073623-62073673	Hela-S3	cervix:	n/a
12	chr5:62072660-62072710	HL-60	blood:	n/a
13	chr5:62073623-62073673	T-47D	breast:	n/a
14	chr5:62074261-62074311	U87	brain:	n/a
15	chr5:62071572-62071622	SK-N-SH_RA	brain:	n/a
16	chr5:62074261-62074311	BJ	skin:	n/a
17	chr5:62072660-62072710	AG10803	skin:	n/a
18	chr5:62073161-62073211	GM12892	blood:	n/a
19	chr5:62100540-62100590	HAEpiC	amniotic membrane:	n/a
20	chr5:62071572-62071622	PANC-1	pancreas:	n/a
21	chr5:62100540-62100590	PFSK-1	brain:	n/a
22	chr5:62074261-62074311	HEEpiC	esophagus:	n/a
23	chr5:62100540-62100590	A549	lung:	n/a
24	chr5:62073161-62073211	GM12878	blood:	n/a
25	chr5:62074261-62074311	AG09319	gingival:	n/a
26	chr5:62073161-62073211	ovcar-3	ovarian:	n/a
27	chr5:62074572-62074622	HCT-116	colon:	n/a
28	chr5:62072660-62072710	SKMC	muscle:	n/a
29	chr5:62073623-62073673	HRCEpiC	kidney:	n/a
30	chr5:62074572-62074622	SKMC	muscle:	n/a
31	chr5:62073161-62073211	HEEpiC	esophagus:	n/a
32	chr5:62365115-62365165	HRPEpiC	eye:	n/a
33	chr5:62071572-62071622	CMK	blood:	n/a
34	chr5:62071572-62071622	HRE	kidney:	n/a
35	chr5:62073623-62073673	SAEC	small airway:	n/a
36	chr5:62074261-62074311	SK-N-SH	brain:	n/a
37	chr5:62073623-62073673	H1-hESC	embryonic stem cell:	embryo
38	chr5:62365115-62365165	NT2-D1	testis:	n/a
39	chr5:62365115-62365165	GM12892	blood:	n/a
40	chr5:62072660-62072710	AG04449	skin:	fetal
41	chr5:62072660-62072710	AG09309	skin:	n/a
42	chr5:62072660-62072710	H1-hESC	embryonic stem cell:	embryo
43	chr5:62073161-62073211	PrEC	prostate:	n/a
44	chr5:62100540-62100590	T-47D	breast:	n/a
45	chr5:62074261-62074311	ECC-1	luminal epithelium:	n/a
46	chr5:62365115-62365165	ProgFib	skin:	n/a
47	chr5:62074572-62074622	NHBE	bronchial:	n/a
48	chr5:62365115-62365165	HepG2	liver:	n/a
49	chr5:62071572-62071622	AG09319	gingival:	n/a
50	chr5:62100540-62100590	PrEC	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:21783831..21784384-chr5:62448794..62449526,2	MCF-7	breast:
2	chr5:62689129..62691869-chr5:62694201..62697545,3	K562	blood:
3	chr5:62688331..62691927-chr5:62694917..62699039,4	K562	blood:
4	chr5:62068406..62072262-chr5:62073628..62078748,5	K562	blood:
5	chr5:62177885..62179876-chr5:62180704..62182544,2	K562	blood:
6	chr5:62069461..62071077-chr5:62076501..62078748,2	K562	blood:
7	chr5:62193925..62195577-chr5:62201485..62203661,2	MCF-7	breast:
8	chr5:62061013..62063521-chr5:62063661..62066191,2	K562	blood:
9	chr17:56736164..56737083-chr5:62632172..62633192,29	MCF-7	breast:
10	chr5:62036443..62039207-chr5:62041195..62044511,3	K562	blood:
11	chr5:62697016..62697521-chr5:63907910..63908892,2	K562	blood:
12	chr17:56734221..56737941-chr5:62631172..62634192,18	MCF-7	breast:
13	chr5:62030684..62032945-chr5:62039649..62042488,2	MCF-7	breast:
14	chr5:62068406..62072262-chr5:62073628..62078748,5	K562	blood:
15	chr5:62078011..62080327-chr5:62081236..62083654,2	K562	blood:
16	chr5:62730491..62733268-chr5:62735229..62737200,2	K562	blood:
17	chr5:62036443..62039207-chr5:62041195..62044511,3	K562	blood:
18	chr5:62729811..62731369-chr5:62732550..62734446,2	MCF-7	breast:
19	chr5:62582710..62584559-chr5:62585298..62587676,2	MCF-7	breast:
20	chr5:62421372..62422126-chr5:63259016..63259610,3	MCF-7	breast:
21	chr5:62729811..62731369-chr5:62732550..62734446,2	MCF-7	breast:
22	chr17:56735268..56738937-chr5:62632672..62634192,8	MCF-7	breast:
23	chr5:62542753..62544427-chr5:62547442..62548997,2	K562	blood:
24	chr5:62681299..62684293-chr5:62685563..62687672,2	K562	blood:
25	chr17:56736153..56736969-chr5:62632172..62633192,8	HCT-116	colon:
26	chr5:62542467..62544427-chr5:62546236..62548997,2	K562	blood:
27	chr5:62412476..62414687-chr5:62419094..62420921,2	K562	blood:
28	chr5:61756022..61757748-chr5:62074424..62075807,9	MCF-7	breast:
29	chr5:62688331..62691927-chr5:62694917..62699039,4	K562	blood:
30	chr5:62503002..62504895-chr5:62506873..62508754,2	MCF-7	breast:
31	chr5:62527630..62529181-chr5:62531232..62533377,2	MCF-7	breast:
32	chr5:61756416..61757318-chr5:62074341..62075268,4	K562	blood:
33	chr5:62071591..62073108-chr5:62074194..62077077,2	K562	blood:
34	chr5:62080331..62084292-chr5:62086443..62088883,3	K562	blood:
35	chr5:5008094..5008743-chr5:62214886..62215776,2	K562	blood:
36	chr5:62730491..62733268-chr5:62735229..62737200,2	K562	blood:
37	chr5:62689129..62691869-chr5:62694201..62697545,3	K562	blood:
38	chr5:62606697..62608384-chr5:62610156..62611740,2	MCF-7	breast:
39	chr5:62349615..62352403-chr5:62352864..62355347,2	MCF-7	breast:
40	chr5:62542753..62544427-chr5:62547442..62548997,2	K562	blood:
41	chr5:62069461..62071077-chr5:62076501..62078748,2	K562	blood:
42	chr5:62421414..62422302-chr5:63258672..63259233,2	MCF-7	breast:
43	chr5:62177885..62179876-chr5:62180704..62182544,2	K562	blood:
44	chr17:56735253..56736865-chr5:62632692..62634192,4	K562	blood:
45	chr5:62744743..62747073-chr5:62749692..62752090,2	K562	blood:
46	chr5:62744743..62747073-chr5:62749692..62752090,2	K562	blood:
47	chr5:62412476..62414687-chr5:62419094..62420921,2	K562	blood:
48	chr5:62535956..62538795-chr5:62539410..62541239,2	K562	blood:
49	chr2:239891948..239892626-chr5:62328345..62328845,2	K562	blood:
50	chr5:62030684..62032945-chr5:62039649..62042488,2	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: 11291 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:11291 , 50 per page) page: 1 2 3 4 5 6 7 ... 226

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146526207	chr5:62025525-62025526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs551203422	chr5:62025575-62025576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571109298	chr5:62025612-62025613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533694641	chr5:62025613-62025614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190158239	chr5:62025647-62025648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567322076	chr5:62025676-62025677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535894062	chr5:62025719-62025720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556105896	chr5:62025725-62025726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs576702499	chr5:62025736-62025737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369453842	chr5:62025750-62025751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs35494150	chr5:62025756-62025757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs59774792	chr5:62025844-62025845	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs559247388	chr5:62025851-62025852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs180986439	chr5:62025870-62025871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185267604	chr5:62025891-62025892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141136971	chr5:62025909-62025910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs36002049	chr5:62025952-62025953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561389142	chr5:62025965-62025966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530188098	chr5:62026070-62026071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543486501	chr5:62026080-62026081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565686557	chr5:62026123-62026124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563691872	chr5:62026148-62026149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531555449	chr5:62026189-62026190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144848987	chr5:62026224-62026225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191208207	chr5:62026238-62026239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527500814	chr5:62026251-62026252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533038697	chr5:62026276-62026277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs183886512	chr5:62026317-62026318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs536333017	chr5:62026350-62026351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542999729	chr5:62026364-62026365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562419945	chr5:62026366-62026367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs146728229	chr5:62026408-62026409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs34548225	chr5:62026434-62026435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs398108993	chr5:62026441-62026442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569635038	chr5:62026466-62026467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs538596150	chr5:62026497-62026498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs559308130	chr5:62026499-62026500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs251169	chr5:62026505-62026506	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs188925170	chr5:62026547-62026548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs191689319	chr5:62026550-62026551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs555185682	chr5:62026580-62026581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs574877808	chr5:62026588-62026589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs6896436	chr5:62026621-62026622	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs183587761	chr5:62026622-62026623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577180502	chr5:62026645-62026646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545760339	chr5:62026672-62026673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs556572218	chr5:62026683-62026684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543475255	chr5:62026694-62026695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187148376	chr5:62026765-62026766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs140293077	chr5:62026792-62026793	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:788 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:62023800-62026200	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr5:62024000-62026400	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr5:62026200-62027000	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr5:62026400-62029800	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr5:62026600-62026800	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr5:62026600-62027200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr5:62026800-62028400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr5:62027000-62027600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
9	chr5:62027600-62028200	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr5:62028200-62029400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr5:62028200-62029400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr5:62028400-62029000	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr5:62029400-62029600	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr5:62032000-62032600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr5:62033200-62033600	Enhancers	Ovary	ovary
16	chr5:62033600-62039400	Weak transcription	Ovary	ovary
17	chr5:62037200-62037800	Enhancers	Fetal Intestine Large	intestine
18	chr5:62037200-62037800	Enhancers	HepG2	liver
19	chr5:62037200-62040000	Enhancers	Fetal Intestine Small	intestine
20	chr5:62037600-62039200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr5:62037800-62038000	Flanking Active TSS	HepG2	liver
22	chr5:62037800-62038200	Weak transcription	Fetal Intestine Large	intestine
23	chr5:62038000-62038200	Enhancers	HepG2	liver
24	chr5:62038200-62038400	Flanking Active TSS	HepG2	liver
25	chr5:62038200-62039200	Enhancers	Brain Germinal Matrix	brain
26	chr5:62038200-62040200	Enhancers	Fetal Intestine Large	intestine
27	chr5:62038400-62039400	Enhancers	A549	lung
28	chr5:62038400-62040400	Enhancers	HepG2	liver
29	chr5:62038600-62039000	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr5:62039200-62039600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr5:62039200-62039600	Weak transcription	Brain Germinal Matrix	brain
32	chr5:62039400-62039800	Enhancers	Ovary	ovary
33	chr5:62039400-62040200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr5:62039600-62040000	Enhancers	Brain Germinal Matrix	brain
35	chr5:62039600-62040400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr5:62040000-62040400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr5:62040200-62045200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr5:62045200-62045600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr5:62048000-62048600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
40	chr5:62048000-62049200	Active TSS	A549	lung
41	chr5:62048000-62049200	Active TSS	Hela-S3	cervix
42	chr5:62048200-62049000	Active TSS	K562	blood
43	chr5:62048600-62049000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr5:62066600-62067600	Enhancers	Fetal Kidney	kidney
45	chr5:62073800-62074000	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr5:62073800-62074600	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr5:62074000-62074200	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr5:62074000-62074600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr5:62074000-62075000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
50	chr5:62074000-62075400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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