Variant report

Variant	nsv900933
Chromosome Location	chr13:96138087-96215289
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1193)
CpG islands
(count:1223)
Chromatin interactive
region (count:15)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1193 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:96146340-96146763	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:96146399-96146694	K562	blood:	n/a	n/a
3	ARID3A	chr13:96189084-96189142	K562	blood:	n/a	n/a
4	ARID3A	chr13:96187615-96187926	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:96186164-96186478	HepG2	liver:	n/a	n/a
6	ARID3A	chr13:96137375-96138176	K562	blood:	n/a	n/a
7	ATF3	chr13:96187497-96187956	A549	lung:	n/a	n/a
8	ATF3	chr13:96187415-96187961	A549	lung:	n/a	n/a
9	BACH1	chr13:96176765-96177073	K562	blood:	n/a	n/a
10	BACH1	chr13:96146450-96146650	K562	blood:	n/a	n/a
11	BACH1	chr13:96205837-96205896	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr13:96200017-96200025	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr13:96204872-96205188	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr13:96187555-96187853	GM12878	blood:	n/a	chr13:96187647-96187658
15	BATF	chr13:96187480-96187857	GM12878	blood:	n/a	chr13:96187647-96187658
16	BCL3	chr13:96187453-96188083	A549	lung:	n/a	n/a
17	BCL3	chr13:96187541-96187860	GM12878	blood:	n/a	n/a
18	BCL3	chr13:96187374-96187984	A549	lung:	n/a	n/a
19	BHLHE40	chr13:96187943-96188114	K562	blood:	n/a	n/a
20	BHLHE40	chr13:96187591-96187848	HepG2	liver:	n/a	n/a
21	BHLHE40	chr13:96137218-96138480	K562	blood:	n/a	n/a
22	BHLHE40	chr13:96182514-96182651	HepG2	liver:	n/a	n/a
23	BHLHE40	chr13:96175892-96176102	K562	blood:	n/a	n/a
24	BRCA1	chr13:96204815-96205167	H1-hESC	embryonic stem cell:	n/a	n/a
25	CBX3	chr13:96187375-96188033	HCT-116	colon:	n/a	n/a
26	CBX3	chr13:96187323-96188227	HCT-116	colon:	n/a	n/a
27	CCNT2	chr13:96137307-96138248	K562	blood:	n/a	n/a
28	CEBPB	chr13:96182467-96182814	HepG2	liver:	n/a	n/a
29	CEBPB	chr13:96182479-96182793	A549	lung:	n/a	n/a
30	CEBPB	chr13:96182381-96182866	A549	lung:	n/a	n/a
31	CEBPB	chr13:96205967-96206459	H1-hESC	embryonic stem cell:	n/a	chr13:96206334-96206345
32	CEBPB	chr13:96202054-96202198	K562	blood:	n/a	chr13:96202138-96202155 chr13:96202139-96202152
33	CEBPB	chr13:96171172-96171418	HepG2	liver:	n/a	chr13:96171286-96171297
34	CEBPB	chr13:96187371-96187995	A549	lung:	n/a	n/a
35	CEBPB	chr13:96206005-96206463	HepG2	liver:	n/a	chr13:96206334-96206345
36	CEBPB	chr13:96146397-96146664	HepG2	liver:	n/a	n/a
37	CEBPB	chr13:96182463-96182825	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr13:96182480-96182722	K562	blood:	n/a	n/a
39	CEBPB	chr13:96182533-96182685	HepG2	liver:	n/a	n/a
40	CEBPB	chr13:96176509-96176774	K562	blood:	n/a	chr13:96176635-96176646 chr13:96176657-96176668
41	CEBPB	chr13:96182450-96182720	MCF-7	breast:	n/a	n/a
42	CEBPB	chr13:96176485-96176810	HepG2	liver:	n/a	chr13:96176635-96176646 chr13:96176657-96176668
43	CEBPB	chr13:96176472-96176829	Hela-S3	cervix:	n/a	chr13:96176635-96176646 chr13:96176657-96176668
44	CEBPB	chr13:96199763-96200373	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr13:96176483-96176829	IMR90	lung:	n/a	chr13:96176635-96176646 chr13:96176657-96176668
46	CEBPB	chr13:96206114-96206314	K562	blood:	n/a	n/a
47	CEBPB	chr13:96157538-96157755	A549	lung:	n/a	n/a
48	CEBPB	chr13:96202021-96202558	HepG2	liver:	n/a	chr13:96202138-96202155 chr13:96202139-96202152
49	CEBPB	chr13:96200767-96200929	A549	lung:	n/a	n/a
50	CEBPB	chr13:96182376-96182835	ECC-1	luminal epithelium:	n/a	n/a

(count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:96204860-96204910	AG09319	gingival:	n/a
2	chr13:96204978-96205028	K562	blood:	n/a
3	chr13:96204856-96204906	HRCEpiC	kidney:	n/a
4	chr13:96204860-96204910	AG09319	gingival:	n/a
5	chr13:96204978-96205028	K562	blood:	n/a
6	chr13:96204856-96204906	HRCEpiC	kidney:	n/a
7	chr13:96205897-96205947	HCPEpiC	choroid plexus:	n/a
8	chr13:96205897-96205947	U87	brain:	n/a
9	chr13:96205295-96205345	NHBE	bronchial:	n/a
10	chr13:96204917-96204967	SK-N-SH	brain:	n/a
11	chr13:96202378-96202428	HAEpiC	amniotic membrane:	n/a
12	chr13:96205184-96205234	HEK293	kidney:	embryo
13	chr13:96205184-96205234	GM12891	blood:	n/a
14	chr13:96204870-96204920	AG04449	skin:	fetal
15	chr13:96205679-96205729	HIPEpiC	eye:	n/a
16	chr13:96158480-96158530	HCPEpiC	choroid plexus:	n/a
17	chr13:96204856-96204906	Caco-2	colon:	n/a
18	chr13:96205960-96206010	HepG2	liver:	n/a
19	chr13:96204873-96204923	MCF-7	breast:	n/a
20	chr13:96204493-96204543	Jurkat	blood:	n/a
21	chr13:96204978-96205028	AG10803	skin:	n/a
22	chr13:96207681-96207731	NB4	blood:	n/a
23	chr13:96204870-96204920	NH-A	brain:	n/a
24	chr13:96205897-96205947	PANC-1	pancreas:	n/a
25	chr13:96205897-96205947	GM06990	blood:	n/a
26	chr13:96204856-96204906	HIPEpiC	eye:	n/a
27	chr13:96207681-96207731	NHDF-neo	bronchial:	n/a
28	chr13:96204870-96204920	NT2-D1	testis:	n/a
29	chr13:96204669-96204719	NH-A	brain:	n/a
30	chr13:96158480-96158530	HMEC	breast:	n/a
31	chr13:96204493-96204543	HCT-116	colon:	n/a
32	chr13:96205897-96205947	HPAEpiC	pulmonary alveolar:	n/a
33	chr13:96204518-96204568	Hela-S3	cervix:	n/a
34	chr13:96206104-96206154	AG09309	skin:	n/a
35	chr13:96204854-96204904	AoSMC	blood vessel:	n/a
36	chr13:96207681-96207731	LNCaP	prostate:	n/a
37	chr13:96204860-96204910	HL-60	blood:	n/a
38	chr13:96207681-96207731	HMEC	breast:	n/a
39	chr13:96204854-96204904	IMR90	lung:	fetal
40	chr13:96204518-96204568	AG09309	skin:	n/a
41	chr13:96205679-96205729	AG04450	lung:	fetal
42	chr13:96205960-96206010	HIPEpiC	eye:	n/a
43	chr13:96204854-96204904	HUVEC	blood vessel:	n/a
44	chr13:96206104-96206154	LNCaP	prostate:	n/a
45	chr13:96204873-96204923	GM12878	blood:	n/a
46	chr13:96204856-96204906	T-47D	breast:	n/a
47	chr13:96205295-96205345	AG04449	skin:	fetal
48	chr13:96204860-96204910	K562	blood:	n/a
49	chr13:96204917-96204967	HRE	kidney:	n/a
50	chr13:96205184-96205234	ovcar-3	ovarian:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:96148891..96151318-chr13:96153321..96155668,2	K562	blood:
2	chr13:96164126..96166950-chr13:96172138..96174070,2	K562	blood:
3	chr13:96168785..96171227-chr13:96172406..96174921,2	MCF-7	breast:
4	chr13:96158409..96159956-chr13:96164959..96167246,2	MCF-7	breast:
5	chr13:96168785..96171227-chr13:96172406..96174921,2	MCF-7	breast:
6	chr13:96190182..96191726-chr13:96328534..96331216,2	K562	blood:
7	chr13:96158409..96159956-chr13:96164959..96167246,2	MCF-7	breast:
8	chr13:96212339..96214130-chr13:96214370..96217172,2	MCF-7	breast:
9	chr13:96148891..96151318-chr13:96153321..96155668,2	K562	blood:
10	chr13:96146074..96146987-chr13:96215991..96216972,6	MCF-7	breast:
11	chr13:96201255..96203740-chr13:96204747..96207433,2	MCF-7	breast:
12	chr13:96164126..96166950-chr13:96172138..96174070,2	K562	blood:
13	chr13:96189087..96189713-chr13:96275598..96276486,2	MCF-7	breast:
14	chr13:96146062..96146563-chr13:97619520..97620349,2	K562	blood:
15	chr13:96178008..96180996-chr13:96185734..96188672,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DZIP1-2	chr13:96185952-96186164	ENSG00000223392
2	lnc-DZIP1-2	chr13:96149313-96149379	ENSG00000223392
3	lnc-DZIP1-2	chr13:96180748-96180841	NONHSAT034762
4	lnc-DZIP1-2	chr13:96149313-96149381	NONHSAT034762
5	lnc-DZIP1-2	chr13:96185952-96186165	NONHSAT034762
6	lnc-DZIP1-2	chr13:96180746-96180841	ENSG00000223392

No data

Variant related genes	Relation type
CLDN10	TF binding region
CLDN10-AS1	TF binding region
CLDN10	CpG island
CLDN10-AS1	CpG island
ENSG00000223392	chromatin interactions
ENSG00000247400	chromatin interactions
ENSG00000134873	chromatin interactions
ENSG00000102580	chromatin interactions

Extended variants
information (count: 2972 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:2972 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12866697	chr13:96138087-96138088	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs139125419	chr13:96138102-96138103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs28414442	chr13:96138106-96138107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs193156434	chr13:96138113-96138114	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12872431	chr13:96138139-96138140	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs76453160	chr13:96138167-96138168	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs11619150	chr13:96138191-96138192	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs538596774	chr13:96138195-96138196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558700389	chr13:96138196-96138197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs141437150	chr13:96138223-96138224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150824603	chr13:96138274-96138275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs183626387	chr13:96138282-96138283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556996861	chr13:96138283-96138284	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573799864	chr13:96138316-96138317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs116773405	chr13:96138388-96138389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552992593	chr13:96138389-96138390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188223007	chr13:96138397-96138398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545072549	chr13:96138403-96138404	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545408061	chr13:96138527-96138528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565596056	chr13:96138528-96138529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113858962	chr13:96138542-96138543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192761766	chr13:96138555-96138556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs4351928	chr13:96138606-96138607	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs565742695	chr13:96138613-96138614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183683345	chr13:96138615-96138616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs386773598	chr13:96138646-96138647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566506543	chr13:96138681-96138682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs4418933	chr13:96138687-96138688	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs552154827	chr13:96138751-96138752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs11407287	chr13:96138767-96138768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs200845202	chr13:96138772-96138773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs201652554	chr13:96138773-96138774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200354222	chr13:96138774-96138775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs201286347	chr13:96138775-96138776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs199723961	chr13:96138776-96138777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs200375095	chr13:96138777-96138778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs76975474	chr13:96138779-96138780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs368865219	chr13:96138858-96138859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs569143886	chr13:96138887-96138888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs537597470	chr13:96138896-96138897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs140143400	chr13:96139067-96139068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs116618294	chr13:96139114-96139115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536383982	chr13:96139148-96139149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188351737	chr13:96139157-96139158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573128855	chr13:96139159-96139160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192387595	chr13:96139176-96139177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184933784	chr13:96139231-96139232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375865460	chr13:96139250-96139251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563500022	chr13:96139270-96139271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143780464	chr13:96139271-96139272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
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
Metanephric adenoma	20802469	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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Rhabdomyosarcoma	17210683	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	19651601	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Burkitt''s lymphoma	20823134	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:869 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:96127800-96144600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr13:96135800-96138600	Enhancers	Pancreas	Pancrea
3	chr13:96137000-96138400	Enhancers	K562	blood
4	chr13:96137200-96138200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr13:96137200-96138400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr13:96137200-96138400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr13:96137200-96138400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr13:96137200-96138400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr13:96137200-96138400	Enhancers	Right Atrium	heart
10	chr13:96137200-96138600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr13:96137200-96138600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr13:96137200-96138600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr13:96137200-96138600	Enhancers	HMEC	breast
14	chr13:96137200-96138600	Enhancers	HUVEC	blood vessel
15	chr13:96137200-96139000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr13:96137400-96138200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr13:96137400-96138200	Weak transcription	Spleen	Spleen
18	chr13:96137400-96138200	Enhancers	GM12878-XiMat	blood
19	chr13:96137400-96138200	Enhancers	Osteobl	bone
20	chr13:96137400-96138400	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr13:96137400-96138400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr13:96137400-96138400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr13:96137400-96138400	Enhancers	NH-A	brain
24	chr13:96137400-96138600	Enhancers	Primary hematopoietic stem cells	blood
25	chr13:96137400-96138600	Enhancers	NHEK	skin
26	chr13:96137600-96138400	Weak transcription	Esophagus	oesophagus
27	chr13:96137800-96138200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr13:96138000-96138200	Enhancers	NHDF-Ad	bronchial
29	chr13:96138000-96138400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr13:96138200-96138400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr13:96138200-96138400	Enhancers	Spleen	Spleen
32	chr13:96138400-96138600	Enhancers	Esophagus	oesophagus
33	chr13:96138400-96139400	Weak transcription	K562	blood
34	chr13:96138600-96139600	Weak transcription	HMEC	breast
35	chr13:96139400-96139600	Enhancers	K562	blood
36	chr13:96143000-96144200	Weak transcription	HMEC	breast
37	chr13:96143800-96145400	Enhancers	Stomach Mucosa	stomach
38	chr13:96144000-96144200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
39	chr13:96144200-96144600	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr13:96144200-96145000	Enhancers	H1 Cell Line	embryonic stem cell
41	chr13:96144200-96145000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr13:96144200-96145000	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr13:96144200-96145000	Enhancers	HMEC	breast
44	chr13:96144200-96145400	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr13:96144400-96145000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr13:96144600-96145000	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr13:96144600-96145000	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr13:96144600-96145000	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr13:96144600-96145000	Enhancers	Hela-S3	cervix
50	chr13:96144600-96145200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell

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