Variant report

Variant	esv3358042
Chromosome Location	chr5:37232244-37251247
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:435)
CpG islands
(count:488)
Chromatin interactive
region (count:26)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:435 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:37249328-37249415	HepG2	liver:	n/a	n/a
2	ATF2	chr5:37249330-37249721	GM12878	blood:	n/a	n/a
3	BACH1	chr5:37249622-37249625	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr5:37249087-37249607	A549	lung:	n/a	chr5:37249490-37249503 chr5:37249563-37249572
5	BCLAF1	chr5:37248901-37249584	GM12878	blood:	n/a	chr5:37249490-37249503 chr5:37249563-37249572
6	BRCA1	chr5:37248654-37249941	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr5:37248702-37249800	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr5:37249235-37249336	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPD	chr5:37249224-37249794	HepG2	liver:	n/a	n/a
10	CHD1	chr5:37248813-37249206	GM12878	blood:	n/a	n/a
11	CHD1	chr5:37249215-37249393	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr5:37248971-37250080	H1-hESC	embryonic stem cell:	n/a	chr5:37249646-37249656 chr5:37249636-37249646 chr5:37249762-37249772
13	CHD2	chr5:37248652-37250257	Hela-S3	cervix:	n/a	chr5:37249646-37249656 chr5:37249636-37249646 chr5:37249762-37249772
14	CHD2	chr5:37248897-37249636	GM12878	blood:	n/a	n/a
15	CHD2	chr5:37248986-37249489	HepG2	liver:	n/a	n/a
16	CREB1	chr5:37248857-37250008	HepG2	liver:	n/a	n/a
17	CREB1	chr5:37248951-37249922	A549	lung:	n/a	n/a
18	CREB1	chr5:37249181-37249702	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTBP2	chr5:37248902-37250350	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr5:37249240-37249390	HEK293	kidney:	n/a	chr5:37249349-37249358
21	CTCF	chr5:37249040-37249190	NB4	blood:	n/a	n/a
22	CTCF	chr5:37249000-37249150	HepG2	liver:	n/a	n/a
23	CTCF	chr5:37249260-37249410	HEK293	kidney:	n/a	chr5:37249349-37249358
24	CTCF	chr5:37249240-37249390	HMEC	breast:	n/a	chr5:37249349-37249358
25	CTCF	chr5:37249060-37249210	BE2_C	brain:	n/a	n/a
26	CTCF	chr5:37249000-37249150	BJ	skin:	n/a	n/a
27	CTCF	chr5:37249123-37249152	GM13976	blood:	n/a	n/a
28	CTCF	chr5:37249280-37249430	HPAF	blood vessel:	n/a	chr5:37249349-37249358
29	CTCF	chr5:37249360-37249510	HepG2	liver:	n/a	chr5:37249488-37249501
30	CTCF	chr5:37249120-37249410	RPTEC	kidney:	n/a	chr5:37249349-37249358
31	CTCF	chr5:37249080-37249230	GM12871	blood:	n/a	n/a
32	CTCF	chr5:37249350-37249442	MCF-7	breast:	n/a	n/a
33	CTCF	chr5:37249292-37249345	Lung_OC	lung:	n/a	n/a
34	CTCF	chr5:37249060-37249210	SAEC	small airway:	n/a	n/a
35	CTCF	chr5:37249088-37249183	Pancreas_OC	pancreas:	n/a	n/a
36	CTCF	chr5:37249069-37249189	MCF-7	breast:	n/a	n/a
37	CTCF	chr5:37249098-37249158	GM12891	blood:	n/a	n/a
38	CTCF	chr5:37248951-37249503	GM12878	blood:	n/a	chr5:37249349-37249358 chr5:37249488-37249501
39	CTCF	chr5:37249040-37249190	HAc	cerebellar:	n/a	n/a
40	CTCF	chr5:37249240-37249390	BJ	skin:	n/a	chr5:37249349-37249358
41	CTCF	chr5:37248800-37248950	HCM	heart:	n/a	n/a
42	CTCF	chr5:37249280-37249430	GM12866	blood:	n/a	chr5:37249349-37249358
43	CTCF	chr5:37249300-37249450	MCF-7	breast:	n/a	chr5:37249349-37249358
44	CTCF	chr5:37248960-37249110	GM12872	blood:	n/a	n/a
45	CTCF	chr5:37249359-37249546	Pancreas_OC	pancreas:	n/a	chr5:37249488-37249501
46	CTCF	chr5:37249300-37249450	GM12873	blood:	n/a	chr5:37249349-37249358
47	CTCF	chr5:37249240-37249390	AG10803	skin:	n/a	chr5:37249349-37249358
48	CTCF	chr5:37249240-37249390	HFF	foreskin:	n/a	chr5:37249349-37249358
49	CTCF	chr5:37249120-37249270	GM12867	blood:	n/a	n/a
50	CTCF	chr5:37249120-37249199	Fibrobl	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37250092-37250142	SAEC	small airway:	n/a
2	chr5:37248984-37249034	SK-N-MC	brain:	n/a
3	chr5:37251010-37251060	HRE	kidney:	n/a
4	chr5:37250092-37250142	GM06990	blood:	n/a
5	chr5:37249567-37249617	NB4	blood:	n/a
6	chr5:37248984-37249034	NB4	blood:	n/a
7	chr5:37249223-37249273	NT2-D1	testis:	n/a
8	chr5:37249405-37249455	HNPCEpiC	eye:	n/a
9	chr5:37250092-37250142	SK-N-SH	brain:	n/a
10	chr5:37249405-37249455	T-47D	breast:	n/a
11	chr5:37249405-37249455	SAEC	small airway:	n/a
12	chr5:37248984-37249034	HCT-116	colon:	n/a
13	chr5:37249567-37249617	A549	lung:	n/a
14	chr5:37249567-37249617	T-47D	breast:	n/a
15	chr5:37248894-37248944	H1-hESC	embryonic stem cell:	embryo
16	chr5:37249405-37249455	HUVEC	blood vessel:	n/a
17	chr5:37249909-37249959	HNPCEpiC	eye:	n/a
18	chr5:37248894-37248944	HRE	kidney:	n/a
19	chr5:37250092-37250142	NHBE	bronchial:	n/a
20	chr5:37249405-37249455	HCM	heart:	n/a
21	chr5:37248984-37249034	PFSK-1	brain:	n/a
22	chr5:37248984-37249034	Caco-2	colon:	n/a
23	chr5:37248984-37249034	GM12891	blood:	n/a
24	chr5:37248894-37248944	ProgFib	skin:	n/a
25	chr5:37249405-37249455	BJ	skin:	n/a
26	chr5:37250092-37250142	HCF	heart:	n/a
27	chr5:37248984-37249034	NH-A	brain:	n/a
28	chr5:37249405-37249455	HCF	heart:	n/a
29	chr5:37249909-37249959	PANC-1	pancreas:	n/a
30	chr5:37248894-37248944	SKMC	muscle:	n/a
31	chr5:37251010-37251060	Hela-S3	cervix:	n/a
32	chr5:37250092-37250142	Hepatocyte	liver:	n/a
33	chr5:37249223-37249273	T-47D	breast:	n/a
34	chr5:37248984-37249034	SK-N-SH	brain:	n/a
35	chr5:37248984-37249034	HIPEpiC	eye:	n/a
36	chr5:37249405-37249455	AG04450	lung:	fetal
37	chr5:37250092-37250142	A549	lung:	n/a
38	chr5:37249567-37249617	AG09309	skin:	n/a
39	chr5:37249405-37249455	MCF10A-Er-Src	breast:	n/a
40	chr5:37249223-37249273	HNPCEpiC	eye:	n/a
41	chr5:37248894-37248944	MCF-7	breast:	n/a
42	chr5:37249567-37249617	GM19239	blood:	n/a
43	chr5:37249567-37249617	GM12892	blood:	n/a
44	chr5:37249223-37249273	Hela-S3	cervix:	n/a
45	chr5:37249405-37249455	HIPEpiC	eye:	n/a
46	chr5:37249405-37249455	HAEpiC	amniotic membrane:	n/a
47	chr5:37248984-37249034	AoSMC	blood vessel:	n/a
48	chr5:37249405-37249455	NB4	blood:	n/a
49	chr5:37251010-37251060	BE2_C	brain:	n/a
50	chr5:37251010-37251060	AG04449	skin:	fetal

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:52016674..52017877-chr5:37249098..37249636,3	Hela-S3	cervix:
2	chr5:37231083..37232617-chr5:37243518..37245919,2	K562	blood:
3	chr11:75110443..75111008-chr5:37248561..37249187,2	Hela-S3	cervix:
4	chr19:55918635..55919160-chr5:37249246..37250155,2	Hela-S3	cervix:
5	chr12:95867838..95868385-chr5:37249139..37249647,2	Hela-S3	cervix:
6	chr5:37244319..37247437-chr5:37248031..37251100,3	MCF-7	breast:
7	chr5:37249278..37249862-chr6:27805404..27806202,2	Hela-S3	cervix:
8	chr5:37247385..37249387-chr5:37291319..37293555,2	MCF-7	breast:
9	chr11:67888391..67888933-chr5:37248964..37249645,2	Hela-S3	cervix:
10	chr5:37231083..37232617-chr5:37243518..37245919,2	K562	blood:
11	chr5:37230434..37232617-chr5:37243518..37246467,2	K562	blood:
12	chr5:37230434..37232617-chr5:37243518..37246467,2	K562	blood:
13	chr5:37242850..37244799-chr5:37268818..37270992,2	MCF-7	breast:
14	chr17:41465731..41466245-chr5:37249205..37250047,2	Hela-S3	cervix:
15	chr14:64804845..64805497-chr5:37249133..37249826,2	Hela-S3	cervix:
16	chr5:37248619..37249243-chr7:5562577..5563334,2	Hela-S3	cervix:
17	chr5:37244268..37246209-chr5:37246679..37250816,3	MCF-7	breast:
18	chr12:54388997..54389960-chr5:37248812..37249668,2	Hela-S3	cervix:
19	chr19:10612852..10613551-chr5:37248973..37249815,2	NB4	blood:
20	chr19:10222166..10222747-chr5:37249630..37250278,2	NB4	blood:
21	chr12:27397103..27397782-chr5:37248907..37249410,2	Hela-S3	cervix:
22	chr5:37244319..37247437-chr5:37248031..37251100,3	MCF-7	breast:
23	chr5:37239505..37242479-chr5:37244689..37246213,2	MCF-7	breast:
24	chr5:37239505..37242479-chr5:37244689..37246213,2	MCF-7	breast:
25	chr19:11450158..11450732-chr5:37248969..37249920,2	Hela-S3	cervix:
26	chr16:2517911..2518776-chr5:37248952..37249746,2	Hela-S3	cervix:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR70-5	chr5:37248948-37249323	NONHSAT101057
2	lnc-WDR70-5	chr5:37250499-37250654	NONHSAT101058
3	lnc-NUP155-2	chr5:37246277-37246581	NONHSAT101056
4	lnc-WDR70-5	chr5:37249174-37249323	NONHSAT101058

No data

Variant related genes	Relation type
C5orf42	TF binding region
RN7SL37P	TF binding region
C5orf42	CpG island
RN7SL37P	CpG island
ENSG00000113569	chromatin interactions
ENSG00000197603	chromatin interactions
ENSG00000111142	chromatin interactions
ENSG00000079999	chromatin interactions
ENSG00000180806	chromatin interactions
ENSG00000184348	chromatin interactions
ENSG00000259895	chromatin interactions
ENSG00000105514	chromatin interactions
ENSG00000243989	chromatin interactions
ENSG00000110721	chromatin interactions
ENSG00000214770	chromatin interactions
ENSG00000250133	chromatin interactions
ENSG00000244165	chromatin interactions
ENSG00000114779	chromatin interactions
ENSG00000149273	chromatin interactions
ENSG00000108106	chromatin interactions
ENSG00000242493	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000211455	chromatin interactions

Extended variants
information (count: 660 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:660 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550377966	chr5:37232283-37232284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs568556989	chr5:37232329-37232330	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192864264	chr5:37232347-37232348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547456933	chr5:37232348-37232349	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs146017774	chr5:37232350-37232351	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573391591	chr5:37232376-37232377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547645506	chr5:37232512-37232513	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566135002	chr5:37232513-37232514	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542120481	chr5:37232573-37232574	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183160901	chr5:37232574-37232575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558385364	chr5:37232594-37232595	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs36033877	chr5:37232624-37232625	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs70976286	chr5:37232642-37232643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570683693	chr5:37232643-37232644	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562426127	chr5:37232657-37232658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113147370	chr5:37232736-37232737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191943524	chr5:37232766-37232767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs113308412	chr5:37232776-37232777	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556372277	chr5:37232797-37232798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183612622	chr5:37232799-37232800	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139972285	chr5:37232807-37232808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539371637	chr5:37232851-37232852	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141711343	chr5:37232860-37232861	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs35187367	chr5:37232868-37232869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374392426	chr5:37232903-37232904	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs141724654	chr5:37232941-37232942	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs71619845	chr5:37232964-37232965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200452582	chr5:37232965-37232966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs71619846	chr5:37232968-37232969	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572486068	chr5:37232971-37232972	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs146247019	chr5:37233021-37233022	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564302152	chr5:37233036-37233037	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs368289918	chr5:37233071-37233072	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs58282784	chr5:37233079-37233080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188322877	chr5:37233158-37233159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564561772	chr5:37233180-37233181	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543541377	chr5:37233217-37233218	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561955920	chr5:37233257-37233258	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529400663	chr5:37233285-37233286	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547705820	chr5:37233289-37233290	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs193219191	chr5:37233290-37233291	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs148423944	chr5:37233308-37233309	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs201991145	chr5:37233310-37233311	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142405113	chr5:37233345-37233346	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs552180527	chr5:37233357-37233358	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs570351680	chr5:37233390-37233391	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs185638020	chr5:37233417-37233418	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs555937304	chr5:37233419-37233420	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs568281914	chr5:37233434-37233435	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs13177573	chr5:37233437-37233438	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:98)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	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
Bladder cancer	21909424	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
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1007 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37170400-37235600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr5:37171600-37249000	Weak transcription	Spleen	Spleen
3	chr5:37198400-37236200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr5:37209400-37234800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr5:37209600-37233400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr5:37209600-37239800	Weak transcription	Small Intestine	intestine
7	chr5:37209600-37240200	Weak transcription	Colonic Mucosa	Colon
8	chr5:37209600-37248000	Weak transcription	Gastric	stomach
9	chr5:37209600-37248400	Weak transcription	NHEK	skin
10	chr5:37211200-37237400	Weak transcription	Rectal Smooth Muscle	rectum
11	chr5:37211800-37232600	Weak transcription	Esophagus	oesophagus
12	chr5:37211800-37234400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr5:37213400-37236200	Weak transcription	Right Ventricle	heart
14	chr5:37214000-37233600	Weak transcription	Fetal Brain Male	brain
15	chr5:37215000-37237000	Weak transcription	Fetal Heart	heart
16	chr5:37215000-37248400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr5:37215200-37232400	Weak transcription	Primary T cells from cord blood	blood
18	chr5:37215200-37233800	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr5:37215200-37234000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr5:37215200-37248200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr5:37216600-37233200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr5:37216600-37237000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr5:37216600-37248000	Weak transcription	Pancreas	Pancrea
24	chr5:37217000-37233200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr5:37218800-37233400	Weak transcription	GM12878-XiMat	blood
26	chr5:37221200-37232400	Strong transcription	HSMM	muscle
27	chr5:37221200-37236400	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr5:37221800-37235800	Weak transcription	Left Ventricle	heart
29	chr5:37223000-37233200	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr5:37223400-37236800	Weak transcription	Brain Angular Gyrus	brain
31	chr5:37223600-37237600	Weak transcription	Psoas Muscle	Psoas
32	chr5:37223800-37233400	Weak transcription	Brain Hippocampus Middle	brain
33	chr5:37223800-37233600	Weak transcription	Fetal Brain Female	brain
34	chr5:37224200-37232600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr5:37224200-37247200	Weak transcription	HUVEC	blood vessel
36	chr5:37224800-37236200	Weak transcription	A549	lung
37	chr5:37225600-37232600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr5:37225600-37232600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr5:37225600-37232600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr5:37225600-37233200	Weak transcription	Cortex derived primary cultured neurospheres	brain
41	chr5:37225600-37233800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr5:37225600-37237600	Weak transcription	Lung	lung
43	chr5:37225600-37238000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr5:37225600-37248600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr5:37225800-37232600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr5:37225800-37232800	Weak transcription	Thymus	Thymus
47	chr5:37226000-37237600	Weak transcription	Aorta	Aorta
48	chr5:37226800-37248000	Weak transcription	HepG2	liver
49	chr5:37227000-37233400	Weak transcription	Brain Germinal Matrix	brain
50	chr5:37227200-37232600	Weak transcription	Brain Anterior Caudate	brain

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