Tag | Content |
---|
EnhancerAtlas ID | HS194-04826 |
Organism | Homo sapiens |
Tissue/cell | Urothelial_cell |
Coordinate | chr5:149961560-149962370 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZBTB18 | MA0698.1 | chr5:149962028-149962041 | CAGCCAGATGTTC | + | 6.32 | ZEB1 | MA0103.3 | chr5:149962308-149962319 | CCCACCTGCCC | + | 6.14 | ZNF263 | MA0528.1 | chr5:149962116-149962137 | CTCTCTACCTCCTTCTCCTCA | - | 6.19 | ZNF263 | MA0528.1 | chr5:149961887-149961908 | TGGGGAGGGGGTGGGGAAGGA | + | 6.4 |
|
| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_23666 | chr5:149961437-149962694 | Colon_Crypt_1 | SE_27995 | chr5:149958870-149972475 | Fetal_Intestine | SE_29147 | chr5:149960782-149971912 | Fetal_Intestine_Large | SE_29818 | chr5:149961261-149962605 | Fetal_Muscle | SE_46676 | chr5:149962077-149962572 | Ovary | SE_52506 | chr5:149961232-149966438 | Small_Intestine | SE_65294 | chr5:149961607-149962836 | Pancreatic_islets |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH05I150581 | chr5 | 149960925 | 149966409 |
|
Enhancer Sequence | CTGAGCAAGT GGCTTAACAT CTCAGAGCTG AAGTTTTCTC ATCTGTTAAC ATGAGGATGA 60 GAGTGTTCAT ATCACAGGCA TAGACACTTG AGATCTCCTA TGTGAGTGCT TAGCAGAGCA 120 GGCCTCTTGG GCAAGTGCAC GAAGGCAGAG GAGTACTGTG GGAATCTGCT AGTGGCCATT 180 AGGTCGCTCC TTCCAGGACC CCCAGGAACC CCTTTCCCCA GGAACAGGCA GGGTCGGTGG 240 GGCTTGAGTG TGCAGACGGG GCTTGGCGGG GTTCTGCGGG TTGGTAATAA ATGAACAGGA 300 AAGGAGATTC CATTACGCAG GAATGTCTGG GGAGGGGGTG GGGAAGGAGC CGGCTCTTCT 360 CCCAGCACCA GCCAGCTCTG CGGTCTTGAT TGATGTGCCT TGCACCGCGG CAGCGGCGGG 420 CCTGGTGGAA AGAGGCCCCT TCACTCACCC TTCCTGGAGC TAGGCCAGCA GCCAGATGTT 480 CCTGGCCTTT GGGGAGCTGG GGTGGGGGCA GGGGAGGCCG GCAGCGGGCC AGAGGGCAGC 540 TGCCCAGACG GCGAACCTCT CTACCTCCTT CTCCTCAGCA GCTGGGCCCA GGTGGCGTTG 600 GCTGTACTGC TGACCTTTGG CCGATGGCTG TCTCTCCTGG ACTTTGGCTC TGTTCAGAAT 660 TGGGGGTGGG GTTCTCACCC ACCCTGTCCT GCTGGGAGAG GCACACAGCT GCCTAGGAAA 720 GGGCTTTCAG CTCCAAAAAG GAAAGTATCC CACCTGCCCA AGGTTCTTGT GTTACCCTGG 780 CCAGAGCCAC AGGGGGAGGT GTGACTGGCA 810
|