| Tag | Content |
|---|
EnhancerAtlas ID | HS194-03079 |
Organism | Homo sapiens |
Tissue/cell | Urothelial_cell |
Coordinate | chr2:97151180-97152340 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr2:97151952-97151970 | GGAAAGCGAAACTTAGCC | + | 6.61 | | RUNX1 | MA0002.2 | chr2:97151283-97151294 | AAACCACAGAG | - | 6.14 | | Sox6 | MA0515.1 | chr2:97151896-97151906 | CCATTGTTTT | + | 6.02 | | Stat4 | MA0518.1 | chr2:97151946-97151960 | CTTCTAGGAAAGCG | + | 6.17 | | ZIC1 | MA0696.1 | chr2:97151220-97151234 | CACCCCCTGCTGTG | + | 6.99 | | ZIC3 | MA0697.1 | chr2:97151220-97151235 | CACCCCCTGCTGTGC | + | 7.14 | | ZIC4 | MA0751.1 | chr2:97151220-97151235 | CACCCCCTGCTGTGC | + | 6.61 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65729 | chr2:97150674-97152957 | 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 |
| GH02I096485 | chr2 | 97150742 | 97153281 |
|
Enhancer Sequence | GCCTCTGCGC CTCAGTTTCC TGGCTATAAA ATGAGAATGT CACCCCCTGC TGTGCCCCTC 60
GCACTTCACA CAGATCTGAG AGAAACAAGC TGGCTGCGCC AGAAAACCAC AGAGGCACCA 120
CCTCTAGATT CCTGTGGAGA TCCTACCACC CATTCCTTCA AAGGAAGGGA CTGGGGAGCA 180
GGGCAGCTGG CAGCAGAGGC TAATCTGCTG TGCAGGTCTG TGGAGGAAGG GACCGTGCGC 240
GGTTCTCTTC CCTCTGCCTC CAGGCTTAGG AGTCATCCCC CACACGCGGG ACCCCCAGTC 300
CCCACTGTAG ACTTCTTCCA AGTGGAATTT CTTCAACAGT TGATCAGCAG GGGGGTCAGG 360
GCGTGCAGTG CAGGGGTGGG GGTGGGGGTT GCGAGAGGAG TGCCATCAGG GAGTAATGCT 420
GGCGAGGCCT CATGAGGACA GCACGCTGGG GCCCTGTGTG CGATGGGCGC CAGGGGCAGG 480
TGACATGGTG GACCCGGTCT CCCCCTTCCC TCTCCAATTG ATCTAACAGA AAGCCTGATG 540
TGAAAGTCTG GACGAGGGAA TTTTCCCATA TCTGCAGGAA AGCCCCGTAG CAGGTCCCTG 600
GAGCCAGCCC GGGCAGGCCT CCGCTTACAG GACGCTAAAG ATCCCTGGTT GCAGTTCTAC 660
TTTCTTTTTA CTGCGTGTAT TCTGCCCCTG TGATAATGAT TCATTACACG CTTCCTCCAT 720
TGTTTTACTC CAGTGACCTC ACGTCAAGGG AACCTGTGAT CTCAGGCTTC TAGGAAAGCG 780
AAACTTAGCC GCAGCCTGCC TCTCTCCCAG CCTGCCTTAC AAGCACTGTG AGTTGCTGGC 840
TGGCCGAGGC CCTGGCAGAT CAGACCTCCT GCAGCCCCAG GGATGGCACG GGCACCGCCA 900
CTCACGCAGC CGGTAGAGCG CTCCTAGGGC AGGCCCATCT CGCTTCCCTC TCGCCTCTCC 960
CCCCCGCTTT TGCTTGGGCC AATCCGACCT CCTCACCTCC TCGTAGCTCC CCCAGCACAC 1020
CTTGCCTTTG CCATCTCTGC ATGTGCCGCG CCTGCTGTCT GGAAGACCGG CATCCATTCC 1080
CCTCTGCCTT CCAAACTCTC CCTGTAGGAC CAGCTCAAAA GGCATCTCCT CTTCAGCTGT 1140
TCCTGCTGCC AGGGCTAATA 1160
|
