Variant report

Variant	esv1807825
Chromosome Location	chr5:68856885-68913840
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:156)
CpG islands
(count:184)
Chromatin interactive
region (count:0)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:156 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:68856954-68857395	GM12878	blood:	n/a	n/a
2	BATF	chr5:68857142-68857346	GM12878	blood:	n/a	n/a
3	BATF	chr5:68897794-68898185	GM12878	blood:	n/a	n/a
4	BATF	chr5:68897780-68898118	GM12878	blood:	n/a	n/a
5	BCL11A	chr5:68897742-68898263	GM12878	blood:	n/a	n/a
6	BCL11A	chr5:68857029-68857406	GM12878	blood:	n/a	n/a
7	BCL11A	chr5:68897862-68898148	GM12878	blood:	n/a	n/a
8	CEBPB	chr5:68857201-68857397	K562	blood:	n/a	n/a
9	CEBPB	chr5:68857055-68857464	K562	blood:	n/a	n/a
10	CEBPD	chr5:68911591-68912003	K562	blood:	n/a	n/a
11	CTCF	chr5:68875399-68875502	Medullo	brain:	n/a	n/a
12	CTCF	chr5:68870845-68870938	Medullo	brain:	n/a	n/a
13	CTCF	chr5:68874019-68874078	GM10248	blood:	n/a	n/a
14	CTCF	chr5:68908378-68908428	Lung_OC	lung:	n/a	n/a
15	CTCF	chr5:68890437-68890536	LNCaP	prostate:	n/a	n/a
16	CTCF	chr5:68890705-68890753	Medullo	brain:	n/a	n/a
17	CTCF	chr5:68870569-68870638	Kidney_OC	kidney:	n/a	n/a
18	CTCF	chr5:68883919-68883967	Medullo	brain:	n/a	n/a
19	EBF1	chr5:68904882-68905202	GM12878	blood:	n/a	n/a
20	EBF1	chr5:68897874-68898259	GM12878	blood:	n/a	n/a
21	EBF1	chr5:68879258-68879506	GM12878	blood:	n/a	n/a
22	EBF1	chr5:68879238-68879448	GM12878	blood:	n/a	n/a
23	ESR1	chr5:68899863-68900234	T-47D	breast:	n/a	n/a
24	ESR1	chr5:68899849-68900262	T-47D	breast:	n/a	n/a
25	FOS	chr5:68857037-68857078	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr5:68857042-68857238	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr5:68857049-68857063	MCF10A-Er-Src	breast:	n/a	n/a
28	FOSL2	chr5:68913375-68913701	HepG2	liver:	n/a	n/a
29	FOSL2	chr5:68856824-68857380	HepG2	liver:	n/a	chr5:68857103-68857114
30	FOSL2	chr5:68863979-68864182	HepG2	liver:	n/a	chr5:68864057-68864064 chr5:68864057-68864065
31	FOSL2	chr5:68863975-68864228	HepG2	liver:	n/a	chr5:68864057-68864064 chr5:68864057-68864065
32	FOSL2	chr5:68856837-68857358	HepG2	liver:	n/a	chr5:68857103-68857114
33	FOSL2	chr5:68910668-68911104	HepG2	liver:	n/a	n/a
34	FOXA1	chr5:68890145-68890685	HepG2	liver:	n/a	n/a
35	FOXA1	chr5:68856742-68857209	HepG2	liver:	n/a	n/a
36	FOXA1	chr5:68863753-68864398	HepG2	liver:	n/a	n/a
37	FOXA1	chr5:68899908-68900311	HepG2	liver:	n/a	n/a
38	FOXA2	chr5:68856874-68857211	A549	lung:	n/a	n/a
39	GATA2	chr5:68890239-68890673	K562	blood:	n/a	n/a
40	GATA2	chr5:68911476-68911916	K562	blood:	n/a	n/a
41	HEY1	chr5:68856852-68857406	K562	blood:	n/a	n/a
42	HEY1	chr5:68856886-68857042	HepG2	liver:	n/a	n/a
43	HEY1	chr5:68858360-68858616	K562	blood:	n/a	n/a
44	IRF4	chr5:68897648-68898539	GM12878	blood:	n/a	n/a
45	IRF4	chr5:68857046-68857384	GM12878	blood:	n/a	n/a
46	IRF4	chr5:68904825-68905228	GM12878	blood:	n/a	n/a
47	IRF4	chr5:68897692-68898345	GM12878	blood:	n/a	n/a
48	JUND	chr5:68863965-68864144	HepG2	liver:	n/a	chr5:68864057-68864064 chr5:68864057-68864065
49	JUND	chr5:68857052-68857089	HepG2	liver:	n/a	n/a
50	JUND	chr5:68857052-68857240	K562	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:68857760-68857810	PrEC	prostate:	n/a
2	chr5:68857760-68857810	PrEC	prostate:	n/a
3	chr5:68857760-68857810	NB4	blood:	n/a
4	chr5:68857760-68857810	NHBE	bronchial:	n/a
5	chr5:68857760-68857810	BJ	skin:	n/a
6	chr5:68868293-68868343	HL-60	blood:	n/a
7	chr5:68868293-68868343	HAEpiC	amniotic membrane:	n/a
8	chr5:68859882-68859932	Jurkat	blood:	n/a
9	chr5:68859882-68859932	ProgFib	skin:	n/a
10	chr5:68868293-68868343	SK-N-SH	brain:	n/a
11	chr5:68857760-68857810	K562	blood:	n/a
12	chr5:68859882-68859932	HEK293	kidney:	embryo
13	chr5:68868293-68868343	SK-N-MC	brain:	n/a
14	chr5:68868293-68868343	GM12892	blood:	n/a
15	chr5:68859882-68859932	AoSMC	blood vessel:	n/a
16	chr5:68857760-68857810	Caco-2	colon:	n/a
17	chr5:68859882-68859932	HCT-116	colon:	n/a
18	chr5:68857760-68857810	ECC-1	luminal epithelium:	n/a
19	chr5:68868293-68868343	SK-N-SH_RA	brain:	n/a
20	chr5:68868293-68868343	IMR90	lung:	fetal
21	chr5:68859882-68859932	H1-hESC	embryonic stem cell:	embryo
22	chr5:68868293-68868343	CMK	blood:	n/a
23	chr5:68868293-68868343	HRCEpiC	kidney:	n/a
24	chr5:68868293-68868343	AG04449	skin:	fetal
25	chr5:68859882-68859932	NHDF-neo	bronchial:	n/a
26	chr5:68868293-68868343	PANC-1	pancreas:	n/a
27	chr5:68868293-68868343	HepG2	liver:	n/a
28	chr5:68859882-68859932	Hepatocyte	liver:	n/a
29	chr5:68859882-68859932	ECC-1	luminal epithelium:	n/a
30	chr5:68857760-68857810	RPTEC	kidney:	n/a
31	chr5:68868293-68868343	RPTEC	kidney:	n/a
32	chr5:68857760-68857810	SK-N-MC	brain:	n/a
33	chr5:68868293-68868343	HCT-116	colon:	n/a
34	chr5:68857760-68857810	GM19239	blood:	n/a
35	chr5:68868293-68868343	HUVEC	blood vessel:	n/a
36	chr5:68859882-68859932	NH-A	brain:	n/a
37	chr5:68859882-68859932	MCF-7	breast:	n/a
38	chr5:68857760-68857810	BE2_C	brain:	n/a
39	chr5:68868293-68868343	AG10803	skin:	n/a
40	chr5:68859882-68859932	A549	lung:	n/a
41	chr5:68859882-68859932	HEEpiC	esophagus:	n/a
42	chr5:68859882-68859932	Hela-S3	cervix:	n/a
43	chr5:68859882-68859932	NB4	blood:	n/a
44	chr5:68857760-68857810	HIPEpiC	eye:	n/a
45	chr5:68868293-68868343	HRE	kidney:	n/a
46	chr5:68857760-68857810	Hepatocyte	liver:	n/a
47	chr5:68868293-68868343	HCM	heart:	n/a
48	chr5:68857760-68857810	AoSMC	blood vessel:	n/a
49	chr5:68857760-68857810	SK-N-SH_RA	brain:	n/a
50	chr5:68868293-68868343	BJ	skin:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OCLN-1	chr5:68858500-68858597	NONHSAT101929
2	lnc-GTF2H2C-1	chr5:68890071-68890550	NONHSAT101931
3	lnc-OCLN-1	chr5:68860927-68860960	NONHSAT101929
4	lnc-GTF2H2C-1	chr5:68889300-68889532	NONHSAT101931

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GTF2H2D	hsa-miR-30a-5p	chr5:68888221-68888242

Variant related genes	Relation type
GTF2H2C	TF binding region
ENSG00000248477	TF binding region
GTF2H2C	CpG island
ENSG00000248477	CpG island

Extended variants
information (count: 296 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2244243	chr5:68856885-68856886	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs2312818	chr5:68856914-68856915	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs529790871	chr5:68856992-68856993	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs144783267	chr5:68857043-68857044	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs373469880	chr5:68857063-68857064	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs376502574	chr5:68857093-68857094	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs560183198	chr5:68857102-68857103	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs371300813	chr5:68857194-68857195	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs374248215	chr5:68857245-68857246	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs527244211	chr5:68857269-68857270	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs552601028	chr5:68857294-68857295	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs565298965	chr5:68857366-68857367	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs201801283	chr5:68857381-68857382	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs567592449	chr5:68857382-68857383	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs536527473	chr5:68857391-68857392	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs111718706	chr5:68857411-68857412	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs571098004	chr5:68857462-68857463	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs531828107	chr5:68857515-68857516	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs181916292	chr5:68857522-68857523	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs568245514	chr5:68857528-68857529	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs535543413	chr5:68857559-68857560	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs534241009	chr5:68857573-68857574	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs547444065	chr5:68857576-68857577	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs559176594	chr5:68857599-68857600	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs565739136	chr5:68857627-68857628	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs539791917	chr5:68857725-68857726	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs367683018	chr5:68857751-68857752	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs3097196	chr5:68857761-68857762	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs117044031	chr5:68857764-68857765	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs185755201	chr5:68857782-68857783	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs556389400	chr5:68857905-68857906	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs574627905	chr5:68857946-68857947	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs556471855	chr5:68858100-68858101	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs190506315	chr5:68858101-68858102	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs199720629	chr5:68858140-68858141	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs560243976	chr5:68858172-68858173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368697182	chr5:68858227-68858228	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs571968820	chr5:68858267-68858268	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs545752953	chr5:68858485-68858486	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs371228068	chr5:68858545-68858546	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs564663668	chr5:68858573-68858574	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs532011858	chr5:68858580-68858581	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs550010574	chr5:68858925-68858926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542301282	chr5:68858926-68858927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529398376	chr5:68858958-68858959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183101377	chr5:68858969-68858970	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186529438	chr5:68858984-68858985	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs118025410	chr5:68859027-68859028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372454225	chr5:68859036-68859037	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs2438094	chr5:68859047-68859048	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ovarian cancer	21781307	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
abnormal development	18461090	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21045282	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelodysplastic syndrome	18663149	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Sezary syndrome	18413736	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21990379	CNVD
Hirschsprung''s Disease	21712996	CNVD
Apoptosis	19488400	CNVD
Breast cancer	22048815	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Acute monocytic leukemia	16498392	CNVD
Colorectal cancer	20459617	CNVD
Gastric adenocarcinoma	19115996	CNVD
Spinal muscular atrophy	17160897	CNVD
Spinal muscular atrophy	17668391	CNVD
Spinal muscular atrophy	17668395	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pseudo-TORCH syndrome	20727516	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Obesity	21131291	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:223 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68855200-68857000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:68855400-68857000	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr5:68855400-68857000	Active TSS	HUES48 Cell Line	embryonic stem cell
4	chr5:68855400-68857000	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr5:68855400-68857000	Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr5:68855400-68857000	Active TSS	iPS-18 Cell Line	embryonic stem cell
7	chr5:68855400-68857000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr5:68855400-68857000	Active TSS	Brain Anterior Caudate	brain
9	chr5:68855400-68857000	Active TSS	Duodenum Smooth Muscle	Duodenum
10	chr5:68855400-68857000	Active TSS	Fetal Intestine Small	intestine
11	chr5:68855400-68857000	Active TSS	Fetal Kidney	kidney
12	chr5:68855400-68857000	Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr5:68855400-68857000	Active TSS	Rectal Mucosa Donor 29	rectum
14	chr5:68855400-68857000	Active TSS	Rectal Smooth Muscle	rectum
15	chr5:68855400-68857000	Active TSS	Right Ventricle	heart
16	chr5:68855400-68857000	Active TSS	Stomach Smooth Muscle	stomach
17	chr5:68855400-68857000	Active TSS	A549	lung
18	chr5:68855400-68857000	Active TSS	GM12878-XiMat	blood
19	chr5:68855400-68857000	Active TSS	K562	blood
20	chr5:68855400-68857000	Active TSS	NHDF-Ad	bronchial
21	chr5:68855400-68857200	Active TSS	HUES64 Cell Line	embryonic stem cell
22	chr5:68855400-68857200	Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr5:68855400-68857200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr5:68855400-68857200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr5:68855600-68857000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr5:68855600-68857000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr5:68855600-68857000	Active TSS	H9 Cell Line	embryonic stem cell
28	chr5:68855600-68857000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr5:68855600-68857000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr5:68855600-68857000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr5:68855600-68857000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr5:68855600-68857000	Active TSS	Breast Myoepithelial Primary Cells	Breast
33	chr5:68855600-68857000	Active TSS	Muscle Satellite Cultured Cells	--
34	chr5:68855600-68857000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr5:68855600-68857000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr5:68855600-68857000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr5:68855600-68857000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr5:68855600-68857000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr5:68855600-68857000	Active TSS	Colonic Mucosa	Colon
40	chr5:68855600-68857000	Active TSS	Fetal Brain Female	brain
41	chr5:68855600-68857000	Active TSS	Pancreas	Pancrea
42	chr5:68855600-68857000	Active TSS	HSMM	muscle
43	chr5:68855600-68857000	Active TSS	HSMMtube	muscle
44	chr5:68855600-68857000	Active TSS	NHLF	lung
45	chr5:68855600-68857000	Active TSS	Osteobl	bone
46	chr5:68855600-68857200	Active TSS	HepG2	liver
47	chr5:68855600-68857200	Active TSS	NH-A	brain
48	chr5:68855800-68857000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
49	chr5:68855800-68857000	Active TSS	Fetal Intestine Large	intestine
50	chr5:68855800-68857200	Active TSS	HMEC	breast

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