Variant report

Variant	nsv909606
Chromosome Location	chr18:44318548-44422661
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:555)
CpG islands
(count:856)
Chromatin interactive
region (count:13)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:555 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:44343741-44343800	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:44411369-44411783	HepG2	liver:	n/a	n/a
3	BACH1	chr18:44335079-44335249	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr18:44336050-44336250	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr18:44334478-44334576	GM12878	blood:	n/a	n/a
6	BHLHE40	chr18:44367638-44367984	GM12878	blood:	n/a	n/a
7	BRCA1	chr18:44318689-44318719	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr18:44403561-44403753	HepG2	liver:	n/a	chr18:44403707-44403718
9	CEBPB	chr18:44420259-44420352	K562	blood:	n/a	n/a
10	CEBPB	chr18:44380339-44380513	HepG2	liver:	n/a	chr18:44380462-44380473
11	CEBPB	chr18:44376072-44376254	A549	lung:	n/a	n/a
12	CEBPB	chr18:44346904-44347188	K562	blood:	n/a	n/a
13	CEBPB	chr18:44376035-44376269	IMR90	lung:	n/a	n/a
14	CEBPB	chr18:44331573-44331857	HepG2	liver:	n/a	chr18:44331721-44331732
15	CEBPB	chr18:44420152-44420395	IMR90	lung:	n/a	n/a
16	CEBPB	chr18:44369682-44369880	HepG2	liver:	n/a	chr18:44369709-44369720
17	CEBPB	chr18:44376072-44376263	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD1	chr18:44336734-44336908	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr18:44334253-44334329	GM12878	blood:	n/a	n/a
20	CHD2	chr18:44336861-44337128	H1-hESC	embryonic stem cell:	n/a	chr18:44337023-44337033
21	CTBP2	chr18:44336144-44337128	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTBP2	chr18:44337460-44338259	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr18:44352471-44352495	GM10266	blood:	n/a	n/a
24	CTCF	chr18:44335100-44335250	HMF	breast:	n/a	n/a
25	CTCF	chr18:44373640-44373790	GM12875	blood:	n/a	chr18:44373713-44373720
26	CTCF	chr18:44352475-44352524	GM10248	blood:	n/a	chr18:44352478-44352499
27	CTCF	chr18:44373720-44373870	HCM	heart:	n/a	n/a
28	CTCF	chr18:44352615-44352658	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr18:44352420-44352570	WERI-Rb-1	eye:	n/a	chr18:44352478-44352499
30	CTCF	chr18:44335066-44335281	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr18:44335060-44335210	HPF	lung:	n/a	n/a
32	CTCF	chr18:44373660-44373810	AG09319	gingival:	n/a	chr18:44373713-44373720
33	CTCF	chr18:44335140-44335290	HA-sp	spinal cord:	n/a	n/a
34	CTCF	chr18:44409980-44410130	HEK293	kidney:	n/a	n/a
35	CTCF	chr18:44352500-44352650	GM06990	blood:	n/a	n/a
36	CTCF	chr18:44336880-44337030	SK-N-SH_RA	brain:	n/a	chr18:44336940-44336953
37	CTCF	chr18:44373500-44373650	NHDF-neo	bronchial:	n/a	n/a
38	CTCF	chr18:44335080-44335230	HCM	heart:	n/a	n/a
39	CTCF	chr18:44373713-44373799	GM12878	blood:	n/a	chr18:44373713-44373720
40	CTCF	chr18:44352420-44352570	GM06990	blood:	n/a	chr18:44352478-44352499
41	CTCF	chr18:44349520-44349670	HEK293	kidney:	n/a	n/a
42	CTCF	chr18:44335140-44335290	GM12871	blood:	n/a	n/a
43	CTCF	chr18:44334980-44335130	HCM	heart:	n/a	n/a
44	CTCF	chr18:44352420-44352570	GM12867	blood:	n/a	chr18:44352478-44352499
45	CTCF	chr18:44334955-44335270	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr18:44335060-44335210	HAc	cerebellar:	n/a	n/a
47	CTCF	chr18:44352367-44352665	GM12878	blood:	n/a	chr18:44352478-44352499
48	CTCF	chr18:44373600-44373750	HCT-116	colon:	n/a	chr18:44373713-44373720
49	CTCF	chr18:44335060-44335210	GM12872	blood:	n/a	n/a
50	CTCF	chr18:44352460-44352610	K562	blood:	n/a	chr18:44352478-44352499

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44392124-44392174	HAEpiC	amniotic membrane:	n/a
2	chr18:44337853-44337903	HIPEpiC	eye:	n/a
3	chr18:44392124-44392174	HAEpiC	amniotic membrane:	n/a
4	chr18:44337853-44337903	HIPEpiC	eye:	n/a
5	chr18:44337664-44337714	HMEC	breast:	n/a
6	chr18:44392124-44392174	HCT-116	colon:	n/a
7	chr18:44337664-44337714	GM12891	blood:	n/a
8	chr18:44335109-44335159	AG04450	lung:	fetal
9	chr18:44339513-44339563	NB4	blood:	n/a
10	chr18:44339513-44339563	HepG2	liver:	n/a
11	chr18:44339513-44339563	PFSK-1	brain:	n/a
12	chr18:44340177-44340227	ECC-1	luminal epithelium:	n/a
13	chr18:44340177-44340227	BJ	skin:	n/a
14	chr18:44336399-44336449	ECC-1	luminal epithelium:	n/a
15	chr18:44339513-44339563	HEK293	kidney:	embryo
16	chr18:44335109-44335159	CMK	blood:	n/a
17	chr18:44337099-44337149	AG09319	gingival:	n/a
18	chr18:44337099-44337149	HCPEpiC	choroid plexus:	n/a
19	chr18:44337099-44337149	HNPCEpiC	eye:	n/a
20	chr18:44334713-44334763	IMR90	lung:	fetal
21	chr18:44337922-44337972	GM12892	blood:	n/a
22	chr18:44336399-44336449	NHDF-neo	bronchial:	n/a
23	chr18:44337910-44337960	K562	blood:	n/a
24	chr18:44337922-44337972	Caco-2	colon:	n/a
25	chr18:44337099-44337149	SK-N-SH_RA	brain:	n/a
26	chr18:44337853-44337903	SK-N-MC	brain:	n/a
27	chr18:44335109-44335159	MCF10A-Er-Src	breast:	n/a
28	chr18:44392124-44392174	Caco-2	colon:	n/a
29	chr18:44338147-44338197	Hela-S3	cervix:	n/a
30	chr18:44392124-44392174	PFSK-1	brain:	n/a
31	chr18:44336399-44336449	CMK	blood:	n/a
32	chr18:44392124-44392174	AG04449	skin:	fetal
33	chr18:44336399-44336449	HNPCEpiC	eye:	n/a
34	chr18:44335109-44335159	NHBE	bronchial:	n/a
35	chr18:44339513-44339563	AG09319	gingival:	n/a
36	chr18:44337910-44337960	HEEpiC	esophagus:	n/a
37	chr18:44339513-44339563	AG09309	skin:	n/a
38	chr18:44340177-44340227	SK-N-SH	brain:	n/a
39	chr18:44334713-44334763	GM12892	blood:	n/a
40	chr18:44333130-44333180	AG09309	skin:	n/a
41	chr18:44340177-44340227	AG10803	skin:	n/a
42	chr18:44392124-44392174	RPTEC	kidney:	n/a
43	chr18:44336399-44336449	Caco-2	colon:	n/a
44	chr18:44337922-44337972	NHBE	bronchial:	n/a
45	chr18:44336399-44336449	Jurkat	blood:	n/a
46	chr18:44340177-44340227	Caco-2	colon:	n/a
47	chr18:44338147-44338197	CMK	blood:	n/a
48	chr18:44333130-44333180	NB4	blood:	n/a
49	chr18:44337099-44337149	GM06990	blood:	n/a
50	chr18:44339513-44339563	HCPEpiC	choroid plexus:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:44339087..44341037-chr18:44341994..44343919,2	K562	blood:
2	chr18:44421049..44423857-chr18:44426853..44428509,2	K562	blood:
3	chr18:44412054..44414419-chr18:44417196..44419147,2	K562	blood:
4	chr18:44414570..44416469-chr18:44421585..44424246,2	K562	blood:
5	chr18:44409358..44411330-chr18:44412581..44415126,2	K562	blood:
6	chr18:44407516..44409436-chr18:44454245..44456431,2	K562	blood:
7	chr18:44385414..44388216-chr18:44388494..44390320,2	MCF-7	breast:
8	chr18:44385414..44388216-chr18:44388494..44390320,2	MCF-7	breast:
9	chr18:44384558..44388431-chr18:44394161..44395866,3	K562	blood:
10	chr18:44409358..44411330-chr18:44412581..44415126,2	K562	blood:
11	chr18:44384558..44388431-chr18:44394161..44395866,3	K562	blood:
12	chr18:44414570..44416469-chr18:44421585..44424246,2	K562	blood:
13	chr18:44412054..44414419-chr18:44417196..44419147,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KATNAL2-7	chr18:44383140-44387340	NONHSAT059143
2	lnc-KATNAL2-1	chr18:44336896-44336994	ENSG00000270112.2
3	lnc-KATNAL2-1	chr18:44339774-44340307	ENSG00000270112.2
4	lnc-KATNAL2-1	chr18:44339687-44344371	NONHSAT059142
5	lnc-KATNAL2-1	chr18:44336450-44336587	ENSG00000270112.2
6	lnc-KATNAL2-1	chr18:44337689-44338426	NONHSAT059140
7	lnc-KATNAL2-1	chr18:44336746-44337039	ENSG00000270112.2
8	lnc-PIAS2-1	chr18:44383187-44383857	ENSG00000267167.1
9	lnc-KATNAL2-1	chr18:44338415-44338422	XLOC_012667
10	lnc-KATNAL2-1	chr18:44338764-44339028	NONHSAT059140
11	lnc-KATNAL2-1	chr18:44339972-44340204	XLOC_012667

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PIAS2	hsa-miR-26b-5p	chr18:44392379-44392395

Variant related genes	Relation type
ENSG00000270112	TF binding region
ST8SIA5	TF binding region
ENSG00000267167	TF binding region
ENSG00000270112	CpG island
ST8SIA5	CpG island
ENSG00000267167	CpG island
ENSG00000101638	chromatin interactions

Extended variants
information (count: 3654 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:3654 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8098387	chr18:44318548-44318549	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs547530755	chr18:44318558-44318559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs567339882	chr18:44318559-44318560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs542179918	chr18:44318567-44318568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529946881	chr18:44318574-44318575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375488545	chr18:44318638-44318639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569652284	chr18:44318643-44318644	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538615840	chr18:44318665-44318666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs8098541	chr18:44318691-44318692	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs372714015	chr18:44318723-44318724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563885072	chr18:44318734-44318735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561533138	chr18:44318749-44318750	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs58248435	chr18:44318754-44318755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs180885088	chr18:44318756-44318757	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574912875	chr18:44318781-44318782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528406628	chr18:44318838-44318839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557652625	chr18:44318839-44318840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577632054	chr18:44319092-44319093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185783206	chr18:44319099-44319100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192457496	chr18:44319110-44319111	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572048172	chr18:44319111-44319112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs139231571	chr18:44319147-44319148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561069718	chr18:44319159-44319160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529836027	chr18:44319168-44319169	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369924678	chr18:44319186-44319187	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10468985	chr18:44319205-44319206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs116141212	chr18:44319227-44319228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183850126	chr18:44319326-44319327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552091926	chr18:44319330-44319331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143143214	chr18:44319341-44319342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535043446	chr18:44319399-44319400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187077711	chr18:44319406-44319407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568555894	chr18:44319418-44319419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190430463	chr18:44319429-44319430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs562173372	chr18:44319454-44319455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372479971	chr18:44319488-44319489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182787887	chr18:44319499-44319500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187031927	chr18:44319543-44319544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147477199	chr18:44319596-44319597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs77972308	chr18:44319599-44319600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571925829	chr18:44319689-44319690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs77520787	chr18:44319690-44319691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191517235	chr18:44319698-44319699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116059977	chr18:44319739-44319740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148513161	chr18:44319768-44319769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563131738	chr18:44319830-44319831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533206573	chr18:44319864-44319865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs141821609	chr18:44319924-44319925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187593032	chr18:44319981-44319982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs482351	chr18:44320004-44320005	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16912164	CNVD
Lung cancer	18438408	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21508638	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16461302	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Pilomyxoid astrocytoma	17436254	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
Burkitt''s lymphoma	18698080	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	16891809	CNVD
Idiopathic thrombocytopenic purpura	19566914	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	21569311	CNVD
small cell lung cancer	17426248	CNVD
Prostate cancer	22341455	CNVD
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1206 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44312600-44319600	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr18:44316000-44318600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr18:44316400-44318600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr18:44316600-44318800	Weak transcription	Brain Angular Gyrus	brain
5	chr18:44318400-44319200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr18:44318600-44318800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr18:44318600-44319000	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr18:44318600-44319000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
9	chr18:44318800-44319000	Enhancers	Brain Angular Gyrus	brain
10	chr18:44319200-44329600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr18:44329600-44334400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr18:44330400-44330800	Enhancers	Brain Germinal Matrix	brain
13	chr18:44330600-44330800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr18:44330600-44330800	Enhancers	Brain Angular Gyrus	brain
15	chr18:44330800-44331800	Weak transcription	Brain Germinal Matrix	brain
16	chr18:44330800-44334200	Weak transcription	Brain Angular Gyrus	brain
17	chr18:44331800-44332400	Active TSS	Brain Germinal Matrix	brain
18	chr18:44332000-44332200	Bivalent Enhancer	HMEC	breast
19	chr18:44332000-44332600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr18:44332000-44332800	Bivalent Enhancer	NHEK	skin
21	chr18:44332000-44333000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr18:44332200-44332400	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr18:44332200-44332400	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr18:44332200-44332400	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr18:44332200-44332400	Enhancers	HMEC	breast
26	chr18:44332200-44332600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr18:44332400-44333000	Flanking Active TSS	Brain Germinal Matrix	brain
28	chr18:44332400-44333000	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr18:44332400-44333000	Bivalent/Poised TSS	Fetal Brain Female	brain
30	chr18:44332400-44334200	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr18:44332600-44332800	Enhancers	Right Atrium	heart
32	chr18:44332600-44335000	Weak transcription	HSMMtube	muscle
33	chr18:44332800-44333200	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr18:44332800-44334600	Weak transcription	Right Atrium	heart
35	chr18:44333000-44333200	Active TSS	Brain Germinal Matrix	brain
36	chr18:44333000-44334000	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr18:44333200-44333400	Flanking Active TSS	Brain Germinal Matrix	brain
38	chr18:44333200-44333600	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr18:44333400-44333600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr18:44333400-44333600	Active TSS	Brain Germinal Matrix	brain
41	chr18:44333600-44333800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr18:44333600-44333800	Flanking Active TSS	Brain Germinal Matrix	brain
43	chr18:44333600-44333800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr18:44333600-44334600	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr18:44333600-44337400	Bivalent/Poised TSS	Fetal Brain Female	brain
46	chr18:44333800-44334000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
47	chr18:44333800-44334000	Active TSS	Brain Germinal Matrix	brain
48	chr18:44333800-44334000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
49	chr18:44333800-44334600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr18:44333800-44334600	Bivalent Enhancer	Fetal Muscle Leg	muscle

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