Variant report

Variant	nsv909515
Chromosome Location	chr18:28556767-28584556
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:28579076-28579371	HepG2	liver:	n/a	n/a
2	ATF3	chr18:28567365-28567764	K562	blood:	n/a	n/a
3	BACH1	chr18:28559038-28559121	K562	blood:	n/a	n/a
4	BCL3	chr18:28565645-28566202	GM12878	blood:	n/a	n/a
5	BCL3	chr18:28565565-28566218	GM12878	blood:	n/a	n/a
6	BHLHE40	chr18:28567429-28567823	K562	blood:	n/a	n/a
7	CBX3	chr18:28567269-28567924	HCT-116	colon:	n/a	n/a
8	CCNT2	chr18:28568199-28568261	K562	blood:	n/a	n/a
9	CEBPB	chr18:28567063-28567818	K562	blood:	n/a	chr18:28567195-28567204 chr18:28567195-28567206 chr18:28567195-28567204 chr18:28567195-28567204 chr18:28567193-28567204 chr18:28567193-28567206 chr18:28567195-28567204
10	CEBPB	chr18:28567480-28567900	MCF-7	breast:	n/a	n/a
11	CEBPB	chr18:28578145-28578319	A549	lung:	n/a	n/a
12	CEBPB	chr18:28567071-28567285	HepG2	liver:	n/a	chr18:28567195-28567204 chr18:28567195-28567206 chr18:28567195-28567204 chr18:28567195-28567204 chr18:28567193-28567204 chr18:28567193-28567206 chr18:28567195-28567204
13	CEBPB	chr18:28567533-28567769	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr18:28567414-28567894	MCF-7	breast:	n/a	n/a
15	CEBPB	chr18:28567174-28568016	HCT-116	colon:	n/a	chr18:28567195-28567204 chr18:28567195-28567206 chr18:28567195-28567204 chr18:28567195-28567204 chr18:28567193-28567204 chr18:28567193-28567206 chr18:28567195-28567204
16	CEBPB	chr18:28567093-28567877	Hela-S3	cervix:	n/a	chr18:28567195-28567204 chr18:28567195-28567206 chr18:28567195-28567204 chr18:28567195-28567204 chr18:28567193-28567204 chr18:28567193-28567206 chr18:28567195-28567204
17	CHD2	chr18:28567431-28567763	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr18:28579240-28579390	GM06990	blood:	n/a	chr18:28579341-28579362
19	CTCF	chr18:28565772-28565993	MCF-7	breast:	n/a	n/a
20	CTCF	chr18:28579270-28579403	Hela-S3	cervix:	n/a	chr18:28579341-28579362
21	CTCF	chr18:28579280-28579430	HMF	breast:	n/a	chr18:28579341-28579362
22	CTCF	chr18:28579240-28579390	HCPEpiC	choroid plexus:	n/a	chr18:28579341-28579362
23	CTCF	chr18:28579280-28579430	HPAF	blood vessel:	n/a	chr18:28579341-28579362
24	CTCF	chr18:28579305-28579392	GM13977	blood:	n/a	chr18:28579341-28579362
25	CTCF	chr18:28579245-28579414	K562	blood:	n/a	chr18:28579341-28579362
26	CTCF	chr18:28580360-28580510	GM06990	blood:	n/a	n/a
27	CTCF	chr18:28579291-28579410	GM10266	blood:	n/a	chr18:28579341-28579362
28	CTCF	chr18:28580321-28580458	K562	blood:	n/a	n/a
29	CTCF	chr18:28579237-28579432	HepG2	liver:	n/a	chr18:28579341-28579362
30	CTCF	chr18:28579270-28579398	HUVEC	blood vessel:	n/a	chr18:28579341-28579362
31	CTCF	chr18:28579110-28579519	MCF-7	breast:	n/a	chr18:28579341-28579362
32	CTCF	chr18:28567260-28567410	HCT-116	colon:	n/a	n/a
33	CTCF	chr18:28578860-28579010	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr18:28579360-28579510	RPTEC	kidney:	n/a	n/a
35	CTCF	chr18:28579266-28579428	LNCaP	prostate:	n/a	chr18:28579341-28579362
36	CTCF	chr18:28579149-28579576	K562	blood:	n/a	chr18:28579341-28579362
37	CTCF	chr18:28579180-28579330	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr18:28579161-28579526	GM12878	blood:	n/a	chr18:28579341-28579362
39	CTCF	chr18:28579193-28579460	A549	lung:	n/a	chr18:28579341-28579362
40	CTCF	chr18:28579240-28579390	GM12865	blood:	n/a	chr18:28579341-28579362
41	CTCF	chr18:28579340-28579490	RPTEC	kidney:	n/a	chr18:28579341-28579362
42	CTCF	chr18:28579292-28579385	GM10248	blood:	n/a	chr18:28579341-28579362
43	CTCF	chr18:28579220-28579370	HPAF	blood vessel:	n/a	chr18:28579341-28579362
44	CTCF	chr18:28579273-28579421	Pancreas_OC	pancreas:	n/a	chr18:28579341-28579362
45	CTCF	chr18:28579265-28579429	LNCaP	prostate:	n/a	chr18:28579341-28579362
46	CTCF	chr18:28579044-28579550	HCT-116	colon:	n/a	chr18:28579341-28579362
47	CTCF	chr18:28565983-28566055	MCF-7	breast:	n/a	n/a
48	CTCF	chr18:28565803-28565947	MCF-7	breast:	n/a	n/a
49	CTCF	chr18:28579240-28579390	HL-60	blood:	n/a	chr18:28579341-28579362
50	CTCF	chr18:28579177-28579502	IMR90	lung:	n/a	chr18:28579341-28579362

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:28572450-28572500	GM06990	blood:	n/a
2	chr18:28572450-28572500	NHBE	bronchial:	n/a
3	chr18:28572450-28572500	HRE	kidney:	n/a
4	chr18:28572450-28572500	HL-60	blood:	n/a
5	chr18:28572450-28572500	GM12891	blood:	n/a
6	chr18:28572450-28572500	Hela-S3	cervix:	n/a
7	chr18:28572450-28572500	HCPEpiC	choroid plexus:	n/a
8	chr18:28572450-28572500	SK-N-SH_RA	brain:	n/a
9	chr18:28572450-28572500	HAEpiC	amniotic membrane:	n/a
10	chr18:28572450-28572500	HEK293	kidney:	embryo
11	chr18:28572450-28572500	HUVEC	blood vessel:	n/a
12	chr18:28572450-28572500	MCF-7	breast:	n/a
13	chr18:28572450-28572500	Jurkat	blood:	n/a
14	chr18:28572450-28572500	GM19239	blood:	n/a
15	chr18:28572450-28572500	BJ	skin:	n/a
16	chr18:28572450-28572500	RPTEC	kidney:	n/a
17	chr18:28572450-28572500	NH-A	brain:	n/a
18	chr18:28572450-28572500	PANC-1	pancreas:	n/a
19	chr18:28572450-28572500	HCM	heart:	n/a
20	chr18:28572450-28572500	GM12878	blood:	n/a
21	chr18:28572450-28572500	Hepatocyte	liver:	n/a
22	chr18:28572450-28572500	AoSMC	blood vessel:	n/a
23	chr18:28572450-28572500	ovcar-3	ovarian:	n/a
24	chr18:28572450-28572500	MCF10A-Er-Src	breast:	n/a
25	chr18:28572450-28572500	HIPEpiC	eye:	n/a
26	chr18:28572450-28572500	NB4	blood:	n/a
27	chr18:28572450-28572500	HNPCEpiC	eye:	n/a
28	chr18:28572450-28572500	AG10803	skin:	n/a
29	chr18:28572450-28572500	SK-N-SH	brain:	n/a
30	chr18:28572450-28572500	GM12892	blood:	n/a
31	chr18:28572450-28572500	LNCaP	prostate:	n/a
32	chr18:28572450-28572500	PFSK-1	brain:	n/a
33	chr18:28572450-28572500	AG04449	skin:	fetal
34	chr18:28572450-28572500	Caco-2	colon:	n/a
35	chr18:28572450-28572500	BE2_C	brain:	n/a
36	chr18:28572450-28572500	H1-hESC	embryonic stem cell:	embryo
37	chr18:28572450-28572500	NT2-D1	testis:	n/a
38	chr18:28572450-28572500	HRPEpiC	eye:	n/a
39	chr18:28572450-28572500	T-47D	breast:	n/a
40	chr18:28572450-28572500	HRCEpiC	kidney:	n/a
41	chr18:28572450-28572500	U87	brain:	n/a
42	chr18:28572450-28572500	SAEC	small airway:	n/a
43	chr18:28572450-28572500	CMK	blood:	n/a
44	chr18:28572450-28572500	AG09309	skin:	n/a
45	chr18:28572450-28572500	HCF	heart:	n/a
46	chr18:28572450-28572500	AG09319	gingival:	n/a
47	chr18:28572450-28572500	HCT-116	colon:	n/a
48	chr18:28572450-28572500	NHDF-neo	bronchial:	n/a
49	chr18:28572450-28572500	PrEC	prostate:	n/a
50	chr18:28572450-28572500	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:28567247..28569402-chr18:28680129..28682819,2	K562	blood:
2	chr18:28551110..28552005-chr18:28559709..28560335,2	MCF-7	breast:
3	chr18:28574400..28576082-chr18:29076395..29079377,2	K562	blood:
4	chr18:28573183..28576916-chr18:28580259..28583981,4	K562	blood:
5	chr17:41445189..41445780-chr18:28568602..28569103,2	NB4	blood:
6	chr18:28570757..28572832-chr18:28637402..28639555,2	MCF-7	breast:
7	chr18:28571461..28573412-chr18:28577844..28580098,2	K562	blood:
8	chr18:28571461..28573412-chr18:28577844..28580098,2	K562	blood:
9	chr18:28557858..28560836-chr18:28681657..28683306,2	K562	blood:
10	chr18:28573183..28576916-chr18:28580259..28583981,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DSC3-1	chr18:28559987-28560046	ENSG00000265670.1
2	lnc-DSC3-1	chr18:28560846-28560883	ENSG00000265670.1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	DSC3	hsa-miR-33a-5p	chr18:28573536-28573558

Variant related genes	Relation type
RNU6-857P	TF binding region
ENSG00000265670	TF binding region
RNU6-857P	CpG island
ENSG00000265670	CpG island
ENSG00000134755	chromatin interactions
ENSG00000265888	chromatin interactions
ENSG00000266521	chromatin interactions
ENSG00000046604	chromatin interactions
ENSG00000261521	chromatin interactions

Extended variants
information (count: 1142 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1142 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545562174	chr18:28557872-28557873	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs187569632	chr18:28557878-28557879	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs532458724	chr18:28557885-28557886	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs72920764	chr18:28557891-28557892	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs545297012	chr18:28557930-28557931	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs9807744	chr18:28557935-28557936	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs537494743	chr18:28557961-28557962	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs191851840	chr18:28558005-28558006	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs77382946	chr18:28558044-28558045	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs182235107	chr18:28558050-28558051	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs560529088	chr18:28558079-28558080	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs559148585	chr18:28558118-28558119	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs139420803	chr18:28558161-28558162	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs538422949	chr18:28558224-28558225	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs537536675	chr18:28558237-28558238	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs556273791	chr18:28558268-28558269	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs574332672	chr18:28558272-28558273	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs542567105	chr18:28558303-28558304	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs368014505	chr18:28558304-28558305	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs560668066	chr18:28558319-28558320	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs150052193	chr18:28558334-28558335	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs186471311	chr18:28558344-28558345	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs374844213	chr18:28558350-28558351	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs528022376	chr18:28558362-28558363	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs545699012	chr18:28558447-28558448	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs564114565	chr18:28558456-28558457	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs368622658	chr18:28558482-28558483	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs544356934	chr18:28558508-28558509	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs563033861	chr18:28558510-28558511	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs112981499	chr18:28558521-28558522	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs548574797	chr18:28558538-28558539	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs560491311	chr18:28558553-28558554	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs16961029	chr18:28558623-28558624	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs372618883	chr18:28558716-28558717	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs552946443	chr18:28558774-28558775	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs75861812	chr18:28558792-28558793	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs565051271	chr18:28558794-28558795	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs538462330	chr18:28558842-28558843	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs191850066	chr18:28558904-28558905	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs568116881	chr18:28558918-28558919	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs546501253	chr18:28558964-28558965	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs16961030	chr18:28558965-28558966	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs182474109	chr18:28558979-28558980	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs144896902	chr18:28559030-28559031	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs539327876	chr18:28559043-28559044	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs188485625	chr18:28559047-28559048	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs576148807	chr18:28559068-28559069	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs72920765	chr18:28559101-28559102	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs561736264	chr18:28559140-28559141	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs72922424	chr18:28559182-28559183	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Esophageal squamous carcinoma	18350619	CNVD
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
Glioblastoma multiforme	21922591	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
Lung cancer	18438408	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
Hepatocellular carcinoma	16750200	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
Breast cancer	17133270	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21297112	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	17002787	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	16912164	CNVD
Renal cell carcinoma	19150565	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19150955	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:142 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:28559200-28559400	Enhancers	K562	blood
2	chr18:28559600-28560600	Weak transcription	K562	blood
3	chr18:28560600-28561000	Enhancers	K562	blood
4	chr18:28560800-28565800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr18:28561200-28561600	Enhancers	Brain Germinal Matrix	brain
6	chr18:28562600-28562800	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr18:28562600-28563000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr18:28563000-28563600	Enhancers	NHEK	skin
9	chr18:28563000-28566800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr18:28563200-28563600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr18:28563200-28565800	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr18:28563600-28565800	Weak transcription	NHEK	skin
13	chr18:28565200-28567200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr18:28565800-28566000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr18:28565800-28566000	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr18:28565800-28566000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr18:28565800-28566000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr18:28565800-28566000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr18:28565800-28566000	Enhancers	Pancreas	Pancrea
20	chr18:28565800-28566000	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr18:28565800-28566000	Enhancers	HMEC	breast
22	chr18:28565800-28566200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr18:28565800-28566200	Enhancers	Esophagus	oesophagus
24	chr18:28565800-28566200	Enhancers	Fetal Brain Male	brain
25	chr18:28565800-28566200	Enhancers	Lung	lung
26	chr18:28565800-28567200	Enhancers	NHEK	skin
27	chr18:28566000-28566200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr18:28566000-28567400	Weak transcription	Pancreas	Pancrea
29	chr18:28566000-28567400	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr18:28566000-28567800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr18:28566200-28567200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr18:28566200-28567200	Weak transcription	HMEC	breast
33	chr18:28566200-28567800	Weak transcription	Fetal Brain Male	brain
34	chr18:28566200-28572400	Weak transcription	Esophagus	oesophagus
35	chr18:28566200-28600600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr18:28566400-28568400	Enhancers	Placenta Amnion	Placenta Amnion
37	chr18:28566800-28569400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr18:28567200-28567400	Enhancers	Hela-S3	cervix
39	chr18:28567200-28567600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr18:28567200-28568200	Enhancers	Fetal Intestine Small	intestine
41	chr18:28567200-28568600	Flanking Active TSS	NHEK	skin
42	chr18:28567200-28568800	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr18:28567200-28568800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr18:28567200-28568800	Enhancers	HMEC	breast
45	chr18:28567400-28567600	Enhancers	Fetal Intestine Large	intestine
46	chr18:28567400-28567600	Enhancers	Pancreas	Pancrea
47	chr18:28567400-28567800	Enhancers	Sigmoid Colon	Sigmoid Colon
48	chr18:28567400-28567800	Enhancers	A549	lung
49	chr18:28567400-28567800	Flanking Active TSS	Hela-S3	cervix
50	chr18:28567400-28567800	Enhancers	K562	blood

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