Variant report

Variant	esv1818108
Chromosome Location	chr18:44519357-44549177
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:527)
CpG islands
(count:1222)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:527 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:44530288-44530439	K562	blood:	n/a	n/a
2	BHLHE40	chr18:44546870-44547457	HepG2	liver:	n/a	n/a
3	BHLHE40	chr18:44547816-44548107	HepG2	liver:	n/a	n/a
4	BRCA1	chr18:44526800-44527412	H1-hESC	embryonic stem cell:	n/a	n/a
5	CBX3	chr18:44519517-44519902	HCT-116	colon:	n/a	n/a
6	CEBPB	chr18:44533294-44533502	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr18:44519633-44519970	IMR90	lung:	n/a	n/a
8	CEBPB	chr18:44519588-44519974	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr18:44519678-44519944	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr18:44540976-44541166	K562	blood:	n/a	n/a
11	CHD2	chr18:44526653-44526788	K562	blood:	n/a	n/a
12	CHD2	chr18:44526479-44527130	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr18:44530100-44530250	HAc	cerebellar:	n/a	chr18:44530204-44530222
14	CTCF	chr18:44530140-44530290	AG04450	lung:	n/a	chr18:44530204-44530222
15	CTCF	chr18:44530100-44530250	HCM	heart:	n/a	chr18:44530204-44530222
16	CTCF	chr18:44530140-44530290	GM12873	blood:	n/a	chr18:44530204-44530222
17	CTCF	chr18:44547459-44547559	GM19239	blood:	n/a	n/a
18	CTCF	chr18:44529860-44530010	WI-38	lung:	n/a	n/a
19	CTCF	chr18:44530160-44530310	GM06990	blood:	n/a	chr18:44530204-44530222
20	CTCF	chr18:44524608-44524631	GM13976	blood:	n/a	n/a
21	CTCF	chr18:44530120-44530270	AG09319	gingival:	n/a	chr18:44530204-44530222
22	CTCF	chr18:44529740-44529890	GM06990	blood:	n/a	n/a
23	CTCF	chr18:44544960-44545110	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr18:44530102-44530337	LNCaP	prostate:	n/a	chr18:44530204-44530222
25	CTCF	chr18:44529867-44530520	A549	lung:	n/a	chr18:44530204-44530222
26	CTCF	chr18:44529060-44529210	GM12873	blood:	n/a	n/a
27	CTCF	chr18:44530180-44530330	GM12868	blood:	n/a	chr18:44530204-44530222
28	CTCF	chr18:44530258-44530261	Lung_OC	lung:	n/a	n/a
29	CTCF	chr18:44530120-44530270	AoAF	blood vessel:	n/a	chr18:44530204-44530222
30	CTCF	chr18:44530160-44530310	HPF	lung:	n/a	chr18:44530204-44530222
31	CTCF	chr18:44529820-44529970	GM12865	blood:	n/a	n/a
32	CTCF	chr18:44529995-44530386	H1-hESC	embryonic stem cell:	n/a	chr18:44530204-44530222
33	CTCF	chr18:44530160-44530310	BJ	skin:	n/a	chr18:44530204-44530222
34	CTCF	chr18:44530160-44530310	GM12864	blood:	n/a	chr18:44530204-44530222
35	CTCF	chr18:44530083-44530358	Medullo	brain:	n/a	chr18:44530204-44530222
36	CTCF	chr18:44547060-44547210	WI-38	lung:	n/a	n/a
37	CTCF	chr18:44530100-44530250	GM12801	blood:	n/a	chr18:44530204-44530222
38	CTCF	chr18:44530120-44530270	HVMF	connective:	n/a	chr18:44530204-44530222
39	CTCF	chr18:44530120-44530270	HCPEpiC	choroid plexus:	n/a	chr18:44530204-44530222
40	CTCF	chr18:44529800-44529950	GM12878	blood:	n/a	n/a
41	CTCF	chr18:44530160-44530310	HRE	kidney:	n/a	chr18:44530204-44530222
42	CTCF	chr18:44547080-44547230	HEK293	kidney:	n/a	n/a
43	CTCF	chr18:44529992-44530406	GM12878	blood:	n/a	chr18:44530204-44530222
44	CTCF	chr18:44530120-44530270	HA-sp	spinal cord:	n/a	chr18:44530204-44530222
45	CTCF	chr18:44530120-44530270	AG10803	skin:	n/a	chr18:44530204-44530222
46	CTCF	chr18:44530120-44530292	Spleen_OC	spleen:	n/a	chr18:44530204-44530222
47	CTCF	chr18:44530140-44530290	WERI-Rb-1	eye:	n/a	chr18:44530204-44530222
48	CTCF	chr18:44527360-44527510	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr18:44530100-44530389	GM12878	blood:	n/a	chr18:44530204-44530222
50	CTCF	chr18:44530120-44530270	GM12865	blood:	n/a	chr18:44530204-44530222

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44525710-44525760	PFSK-1	brain:	n/a
2	chr18:44523070-44523120	K562	blood:	n/a
3	chr18:44525710-44525760	PFSK-1	brain:	n/a
4	chr18:44523070-44523120	K562	blood:	n/a
5	chr18:44543612-44543662	HEEpiC	esophagus:	n/a
6	chr18:44541383-44541433	RPTEC	kidney:	n/a
7	chr18:44526430-44526480	PFSK-1	brain:	n/a
8	chr18:44526867-44526917	HL-60	blood:	n/a
9	chr18:44526700-44526750	RPTEC	kidney:	n/a
10	chr18:44543612-44543662	K562	blood:	n/a
11	chr18:44527026-44527076	HPAEpiC	pulmonary alveolar:	n/a
12	chr18:44526430-44526480	HCF	heart:	n/a
13	chr18:44527026-44527076	T-47D	breast:	n/a
14	chr18:44545807-44545857	LNCaP	prostate:	n/a
15	chr18:44526700-44526750	Hepatocyte	liver:	n/a
16	chr18:44544982-44545032	ovcar-3	ovarian:	n/a
17	chr18:44545807-44545857	HAEpiC	amniotic membrane:	n/a
18	chr18:44526430-44526480	U87	brain:	n/a
19	chr18:44541383-44541433	H1-hESC	embryonic stem cell:	embryo
20	chr18:44545794-44545844	AoSMC	blood vessel:	n/a
21	chr18:44523070-44523120	SAEC	small airway:	n/a
22	chr18:44541383-44541433	BJ	skin:	n/a
23	chr18:44526430-44526480	ECC-1	luminal epithelium:	n/a
24	chr18:44543259-44543309	SK-N-SH_RA	brain:	n/a
25	chr18:44543259-44543309	HCT-116	colon:	n/a
26	chr18:44530218-44530268	GM19239	blood:	n/a
27	chr18:44526605-44526655	ovcar-3	ovarian:	n/a
28	chr18:44545794-44545844	HCF	heart:	n/a
29	chr18:44525710-44525760	AG10803	skin:	n/a
30	chr18:44526867-44526917	HAEpiC	amniotic membrane:	n/a
31	chr18:44526700-44526750	Hela-S3	cervix:	n/a
32	chr18:44525710-44525760	AG04450	lung:	fetal
33	chr18:44526430-44526480	SK-N-SH	brain:	n/a
34	chr18:44545794-44545844	PFSK-1	brain:	n/a
35	chr18:44523070-44523120	PANC-1	pancreas:	n/a
36	chr18:44526430-44526480	HL-60	blood:	n/a
37	chr18:44540890-44540940	LNCaP	prostate:	n/a
38	chr18:44526867-44526917	ECC-1	luminal epithelium:	n/a
39	chr18:44527026-44527076	NHBE	bronchial:	n/a
40	chr18:44540890-44540940	U87	brain:	n/a
41	chr18:44527971-44528021	HNPCEpiC	eye:	n/a
42	chr18:44526756-44526806	H1-hESC	embryonic stem cell:	embryo
43	chr18:44526707-44526757	MCF-7	breast:	n/a
44	chr18:44527026-44527076	Hela-S3	cervix:	n/a
45	chr18:44544982-44545032	A549	lung:	n/a
46	chr18:44525710-44525760	NT2-D1	testis:	n/a
47	chr18:44543612-44543662	GM12891	blood:	n/a
48	chr18:44526756-44526806	SAEC	small airway:	n/a
49	chr18:44543259-44543309	Jurkat	blood:	n/a
50	chr18:44526756-44526806	HL-60	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr18:44494535..44496872-chr18:44526864..44529810,3	MCF-7	breast:
2	chr18:44497069..44499203-chr18:44524229..44526403,2	MCF-7	breast:
3	chr18:44529742..44530665-chr18:44562546..44563169,2	MCF-7	breast:
4	chr18:44526928..44528966-chr18:44543505..44545090,2	MCF-7	breast:

No data

Variant related genes	Relation type
TCEB3CL2	TF binding region
KATNAL2	TF binding region
TCEB3CL2	CpG island
KATNAL2	CpG island
ENSG00000266996	chromatin interactions
ENSG00000078043	chromatin interactions
ENSG00000167216	chromatin interactions

Extended variants
information (count: 1025 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1025 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72917169	chr18:44519393-44519394	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs547363091	chr18:44519458-44519459	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs191342596	chr18:44519470-44519471	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs570976593	chr18:44519499-44519500	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs533627823	chr18:44519546-44519547	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs6507714	chr18:44519574-44519575	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs199713362	chr18:44519576-44519577	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs534650788	chr18:44519581-44519582	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs554690393	chr18:44519587-44519588	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs115981003	chr18:44519613-44519614	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs539943162	chr18:44519624-44519625	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs146362374	chr18:44519626-44519627	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs530903914	chr18:44519663-44519664	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs186715124	chr18:44519711-44519712	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs576975703	chr18:44519749-44519750	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs191176897	chr18:44519771-44519772	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs553401653	chr18:44519773-44519774	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs551006298	chr18:44519810-44519811	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs79308553	chr18:44519850-44519851	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs541853015	chr18:44519858-44519859	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs561953141	chr18:44519863-44519864	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs561587292	chr18:44519901-44519902	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs575663072	chr18:44519933-44519934	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs530320187	chr18:44519937-44519938	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs138357855	chr18:44519991-44519992	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs184730837	chr18:44519996-44519997	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs533607879	chr18:44520024-44520025	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs547309207	chr18:44520026-44520027	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs2187091	chr18:44520048-44520049	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs529629498	chr18:44520145-44520146	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs137863722	chr18:44520163-44520164	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs546930896	chr18:44520172-44520173	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs548181445	chr18:44520280-44520281	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs567062659	chr18:44520348-44520349	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs187583521	chr18:44520358-44520359	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs537111085	chr18:44520394-44520395	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs149583616	chr18:44520413-44520414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs570626270	chr18:44520424-44520425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs36085543	chr18:44520467-44520468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539278718	chr18:44520471-44520472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552830415	chr18:44520483-44520484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566905681	chr18:44520489-44520490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144240351	chr18:44520569-44520570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142488845	chr18:44520600-44520601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192277084	chr18:44520610-44520611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73437174	chr18:44520612-44520613	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs544682896	chr18:44520623-44520624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs72917176	chr18:44520655-44520656	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs118028450	chr18:44520752-44520753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540795966	chr18:44520753-44520754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44515600-44520800	Weak transcription	Psoas Muscle	Psoas
2	chr18:44518400-44521000	Enhancers	HSMM	muscle
3	chr18:44518800-44519400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr18:44518800-44520000	Enhancers	HSMMtube	muscle
5	chr18:44518800-44520200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr18:44518800-44520400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr18:44518800-44520400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr18:44518800-44520800	Enhancers	NHLF	lung
9	chr18:44519000-44520200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr18:44519000-44520200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr18:44519000-44520200	Enhancers	Placenta Amnion	Placenta Amnion
12	chr18:44519000-44520400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr18:44519000-44520800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr18:44519000-44520800	Enhancers	NHDF-Ad	bronchial
15	chr18:44519000-44521000	Enhancers	Muscle Satellite Cultured Cells	--
16	chr18:44519000-44521000	Enhancers	Fetal Muscle Leg	muscle
17	chr18:44519000-44521200	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chr18:44519200-44519600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
19	chr18:44519200-44520800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr18:44519200-44520800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr18:44519200-44520800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr18:44519400-44519600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr18:44519400-44519600	Enhancers	Colon Smooth Muscle	Colon
24	chr18:44519400-44519800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr18:44519400-44519800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr18:44519400-44519800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr18:44519400-44520000	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr18:44519400-44520000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr18:44519400-44520000	Enhancers	HMEC	breast
30	chr18:44519400-44520200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr18:44519400-44520200	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr18:44519400-44520200	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr18:44519400-44520200	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr18:44519400-44520200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr18:44519400-44520200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr18:44519400-44520200	Enhancers	Hela-S3	cervix
37	chr18:44519400-44520400	Enhancers	Osteobl	bone
38	chr18:44519400-44520800	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr18:44519600-44520200	Enhancers	H9 Cell Line	embryonic stem cell
40	chr18:44519600-44520400	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr18:44519600-44521000	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr18:44519800-44520400	Weak transcription	Fetal Muscle Trunk	muscle
43	chr18:44519800-44525400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr18:44520000-44520400	Flanking Active TSS	HSMMtube	muscle
45	chr18:44520000-44526200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr18:44520200-44520400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr18:44520200-44520600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr18:44520200-44521000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr18:44520200-44525400	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr18:44520200-44526200	Weak transcription	H9 Cell Line	embryonic stem cell

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