Variant report

Variant	esv1806101
Chromosome Location	chr13:88771495-88910106
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	CEBPB	chr13:88835715-88836040	A549	lung:	n/a	chr13:88835878-88835889
2	CEBPB	chr13:88776105-88776217	HepG2	liver:	n/a	chr13:88776141-88776152
3	CEBPB	chr13:88835698-88836071	IMR90	lung:	n/a	chr13:88835878-88835889
4	CEBPB	chr13:88835729-88836054	ECC-1	luminal epithelium:	n/a	chr13:88835878-88835889
5	CEBPB	chr13:88863398-88863506	H1-hESC	embryonic stem cell:	n/a	chr13:88863466-88863477 chr13:88863464-88863477 chr13:88863466-88863475 chr13:88863466-88863475 chr13:88863466-88863475 chr13:88863464-88863475 chr13:88863466-88863475
6	CEBPB	chr13:88870153-88870512	Hela-S3	cervix:	n/a	chr13:88870385-88870397 chr13:88870291-88870304 chr13:88870291-88870302 chr13:88870291-88870302 chr13:88870291-88870304
7	CEBPB	chr13:88863332-88863622	HepG2	liver:	n/a	chr13:88863466-88863477 chr13:88863464-88863477 chr13:88863466-88863475 chr13:88863466-88863475 chr13:88863466-88863475 chr13:88863464-88863475 chr13:88863466-88863475
8	CEBPB	chr13:88863340-88863614	A549	lung:	n/a	chr13:88863466-88863477 chr13:88863464-88863477 chr13:88863466-88863475 chr13:88863466-88863475 chr13:88863466-88863475 chr13:88863464-88863475 chr13:88863466-88863475
9	CEBPB	chr13:88862412-88862495	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr13:88889709-88890026	IMR90	lung:	n/a	n/a
11	CEBPB	chr13:88835735-88836046	Hela-S3	cervix:	n/a	chr13:88835878-88835889
12	CEBPB	chr13:88835698-88836053	H1-hESC	embryonic stem cell:	n/a	chr13:88835878-88835889
13	CEBPB	chr13:88835716-88836061	HepG2	liver:	n/a	chr13:88835878-88835889
14	CTCF	chr13:88825200-88825350	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr13:88796900-88797050	BE2_C	brain:	n/a	n/a
16	CTCF	chr13:88848440-88848590	HEK293	kidney:	n/a	n/a
17	CTCF	chr13:88848420-88848570	RPTEC	kidney:	n/a	n/a
18	CTCF	chr13:88848420-88848570	HEEpiC	esophagus:	n/a	n/a
19	CTCF	chr13:88796960-88797110	MCF-7	breast:	n/a	n/a
20	CTCF	chr13:88848522-88848594	LNCaP	prostate:	n/a	n/a
21	CTCF	chr13:88796942-88797174	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr13:88796980-88797130	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr13:88848400-88848550	NHEK	skin:	n/a	n/a
24	CTCF	chr13:88838322-88838326	GM13976	blood:	n/a	n/a
25	CTCF	chr13:88775259-88775272	GM10248	blood:	n/a	n/a
26	CTCF	chr13:88797000-88797150	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr13:88850039-88850051	ProgFib	skin:	n/a	n/a
28	CTCF	chr13:88848420-88848570	HRE	kidney:	n/a	n/a
29	CTCF	chr13:88848440-88848590	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr13:88848371-88848594	GM12878	blood:	n/a	n/a
31	CTCF	chr13:88848477-88848609	Gliobla	brain:	n/a	n/a
32	CTCF	chr13:88848520-88848670	NHEK	skin:	n/a	n/a
33	CTCF	chr13:88848517-88848571	MCF-7	breast:	n/a	n/a
34	CTCF	chr13:88848482-88848598	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr13:88848340-88848490	HRE	kidney:	n/a	n/a
36	CTCF	chr13:88848440-88848590	HCT-116	colon:	n/a	n/a
37	CTCF	chr13:88848400-88848550	HL-60	blood:	n/a	n/a
38	CTCF	chr13:88848516-88848591	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr13:88848517-88848575	LNCaP	prostate:	n/a	n/a
40	CTCF	chr13:88784712-88784735	GM10248	blood:	n/a	n/a
41	CTCF	chr13:88797019-88797061	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr13:88848420-88848570	HPF	lung:	n/a	n/a
43	CTCF	chr13:88848520-88848670	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr13:88848440-88848590	RPTEC	kidney:	n/a	n/a
45	CTCF	chr13:88823800-88824070	HL-60	blood:	n/a	n/a
46	CTCF	chr13:88848460-88848610	BE2_C	brain:	n/a	n/a
47	CTCF	chr13:88848509-88848567	GM12891	blood:	n/a	n/a
48	CTCF	chr13:88797036-88797115	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr13:88799060-88799210	NHLF	lung:	n/a	n/a
50	CTCF	chr13:88900480-88900630	AG10803	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:88788898-88788948	HEEpiC	esophagus:	n/a
2	chr13:88788898-88788948	HRCEpiC	kidney:	n/a
3	chr13:88788898-88788948	HL-60	blood:	n/a
4	chr13:88788898-88788948	GM12891	blood:	n/a
5	chr13:88788987-88789037	PrEC	prostate:	n/a
6	chr13:88788898-88788948	HNPCEpiC	eye:	n/a
7	chr13:88788898-88788948	SK-N-MC	brain:	n/a
8	chr13:88788898-88788948	PrEC	prostate:	n/a
9	chr13:88788898-88788948	BE2_C	brain:	n/a
10	chr13:88788987-88789037	AG04449	skin:	fetal
11	chr13:88788987-88789037	Hepatocyte	liver:	n/a
12	chr13:88788898-88788948	Jurkat	blood:	n/a
13	chr13:88788898-88788948	HCM	heart:	n/a
14	chr13:88788898-88788948	NHDF-neo	bronchial:	n/a
15	chr13:88788898-88788948	GM12878	blood:	n/a
16	chr13:88788987-88789037	HNPCEpiC	eye:	n/a
17	chr13:88788987-88789037	HL-60	blood:	n/a
18	chr13:88788987-88789037	NH-A	brain:	n/a
19	chr13:88788987-88789037	T-47D	breast:	n/a
20	chr13:88788898-88788948	HAEpiC	amniotic membrane:	n/a
21	chr13:88788898-88788948	NT2-D1	testis:	n/a
22	chr13:88788987-88789037	HCT-116	colon:	n/a
23	chr13:88788987-88789037	HIPEpiC	eye:	n/a
24	chr13:88788898-88788948	HCF	heart:	n/a
25	chr13:88788987-88789037	NHBE	bronchial:	n/a
26	chr13:88788898-88788948	MCF-7	breast:	n/a
27	chr13:88788987-88789037	ovcar-3	ovarian:	n/a
28	chr13:88788898-88788948	PFSK-1	brain:	n/a
29	chr13:88788987-88789037	ECC-1	luminal epithelium:	n/a
30	chr13:88788898-88788948	T-47D	breast:	n/a
31	chr13:88788898-88788948	A549	lung:	n/a
32	chr13:88788987-88789037	LNCaP	prostate:	n/a
33	chr13:88788987-88789037	CMK	blood:	n/a
34	chr13:88788987-88789037	ProgFib	skin:	n/a
35	chr13:88788987-88789037	BJ	skin:	n/a
36	chr13:88788898-88788948	HRE	kidney:	n/a
37	chr13:88788987-88789037	HCM	heart:	n/a
38	chr13:88788987-88789037	U87	brain:	n/a
39	chr13:88788898-88788948	BJ	skin:	n/a
40	chr13:88788987-88789037	MCF-7	breast:	n/a
41	chr13:88788898-88788948	ProgFib	skin:	n/a
42	chr13:88788987-88789037	RPTEC	kidney:	n/a
43	chr13:88788987-88789037	Hela-S3	cervix:	n/a
44	chr13:88788898-88788948	SK-N-SH_RA	brain:	n/a
45	chr13:88788987-88789037	GM06990	blood:	n/a
46	chr13:88788987-88789037	HCPEpiC	choroid plexus:	n/a
47	chr13:88788898-88788948	U87	brain:	n/a
48	chr13:88788987-88789037	HRCEpiC	kidney:	n/a
49	chr13:88788987-88789037	NT2-D1	testis:	n/a
50	chr13:88788898-88788948	HCT-116	colon:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK5-5	chr13:88866524-88866575	ENSG00000231019
2	lnc-SLITRK5-5	chr13:88888258-88888337	ENSG00000231019
3	lnc-SLITRK5-5	chr13:88795122-88795355	ENSG00000231019
4	lnc-SLITRK5-5	chr13:88886578-88886673	ENSG00000231019
5	lnc-SLITRK5-5	chr13:88864596-88864694	ENSG00000231019
6	lnc-SLITRK6-18	chr13:88888802-88889224	NONHSAT034610

Variant related genes	Relation type
RPL29P29	TF binding region
ENSG00000223059	TF binding region
ENSG00000231019	TF binding region
RPL29P29	CpG island
ENSG00000223059	CpG island
ENSG00000231019	CpG island

Extended variants
information (count: 1217 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1217 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs180704249	chr13:88775456-88775457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs74583532	chr13:88775511-88775512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573002258	chr13:88775521-88775522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554310268	chr13:88775661-88775662	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572603324	chr13:88775696-88775697	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533644582	chr13:88775714-88775715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558291312	chr13:88775721-88775722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576648671	chr13:88775728-88775729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544103727	chr13:88775774-88775775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs540429814	chr13:88775832-88775833	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184299506	chr13:88775851-88775852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190811771	chr13:88775861-88775862	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370857925	chr13:88775899-88775900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181889016	chr13:88775911-88775912	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs74104475	chr13:88775969-88775970	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs386380096	chr13:88775970-88775971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs386380097	chr13:88775981-88775982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs397689284	chr13:88775982-88775983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186165820	chr13:88776015-88776016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190534542	chr13:88776026-88776027	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376318645	chr13:88776042-88776043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550671053	chr13:88776046-88776047	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547128369	chr13:88776055-88776056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181293882	chr13:88776198-88776199	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs1365696	chr13:88776226-88776227	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs550930308	chr13:88776270-88776271	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs569527141	chr13:88776293-88776294	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs61961760	chr13:88776320-88776321	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs143041341	chr13:88776392-88776393	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs4406933	chr13:88776404-88776405	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs61961761	chr13:88776412-88776413	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs558207723	chr13:88776437-88776438	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs546806893	chr13:88776438-88776439	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs2881382	chr13:88776520-88776521	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs538033910	chr13:88776553-88776554	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs376262136	chr13:88776594-88776595	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs556129661	chr13:88776617-88776618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs148200027	chr13:88776622-88776623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs140160853	chr13:88776671-88776672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs563657203	chr13:88776695-88776696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561230113	chr13:88776703-88776704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs76258085	chr13:88776769-88776770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186346152	chr13:88776787-88776788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs138070563	chr13:88776843-88776844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs143677952	chr13:88776847-88776848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs77377921	chr13:88776863-88776864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs61961762	chr13:88776938-88776939	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs191150221	chr13:88777044-88777045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183037233	chr13:88777073-88777074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs574099108	chr13:88777106-88777107	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Mental retardation	17847001	CNVD
Medulloblastoma	19270706	CNVD
Non-small cell lung cancer	16651412	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
coloboma	21285886	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:88775400-88775600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
2	chr13:88775400-88775600	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr13:88775600-88776200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr13:88775600-88777200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr13:88776200-88776400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr13:88776200-88776600	Active TSS	iPS-20b Cell Line	embryonic stem cell
7	chr13:88776200-88777200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr13:88776200-88777200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr13:88776400-88777000	Enhancers	H1 Cell Line	embryonic stem cell
10	chr13:88776400-88777000	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr13:88776400-88777000	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr13:88776400-88777400	Enhancers	H9 Cell Line	embryonic stem cell
13	chr13:88776600-88777000	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr13:88776600-88777200	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr13:88776600-88777400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr13:88776800-88777200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr13:88777000-88777400	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr13:88784400-88787000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr13:88788400-88788600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr13:88805200-88805800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr13:88805400-88805800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr13:88805400-88807600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr13:88805800-88807000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr13:88807000-88807400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr13:88807200-88807800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr13:88807400-88808000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr13:88808600-88810800	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr13:88810800-88814000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr13:88813800-88815000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr13:88814000-88814600	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr13:88822800-88823000	Active TSS	Pancreas	Pancrea
32	chr13:88828400-88829000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr13:88830200-88831600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr13:88837200-88837600	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr13:88843000-88843200	Enhancers	Pancreas	Pancrea
36	chr13:88855800-88856200	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr13:88855800-88856200	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr13:88855800-88856600	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr13:88855800-88856800	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr13:88856200-88856600	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr13:88856200-88861000	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr13:88861000-88861400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr13:88898400-88898600	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr13:88898600-88898800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr13:88898800-88900400	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr13:88900200-88901000	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr13:88900400-88901200	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr13:88900400-88901200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr13:88900400-88901400	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr13:88900400-88901400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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