| Tag | Content |
|---|
EnhancerAtlas ID | HS091-21232 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:74454290-74455320 |
Target genes | | Number: 31 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF3 | MA0522.2 | chr17:74454901-74454911 | AGCAGGTGTT | - | 6.02 |
|
| | 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 |
| GH17I076458 | chr17 | 74454761 | 74454950 |
|
Enhancer Sequence | CATCTGAGCT GCTTTAGAGA ATGAGACTCA GTAAATTCCT ACCCATCCGA TGGTGTCTTT 60
TATGGACCTC ACTCAGACCC AAGATGCTCT GGATAAGGTT TGAGGCTTGA CTCCTTCCCA 120
GACCCTGAGC CCCCAGCCAC GGTCTCCATA CACTCAGGCT GGCTAGCAGG GTAAGTGTGG 180
ATGGAAGCCG CTGCTTAGTT TTTATTTTTG TCATTGTTGA GGTGTAGGAA GGAGGAAAAA 240
AACTTGATTC CCTAATGAAG AAACCCTCTC TTATCATGGC CCCATCTCCC AGCCTTTCGT 300
GGGGAATAGA GCTATTTCTT GGGAGGATTT CACTTATTTA TAAATGTGCT TCCAGAAACT 360
GAGCTGGTCT GGCCTCTCCC CTTGCTAAGT GGGGTGGGTG GTGTGCAGGA GGCGGCAGAG 420
CCAGCAGCAG AGTGAACTGG TCTCAGGGAA GCAGGCCCTG TCTCGTCCCT ATCTTAACCA 480
GCCACTGGAG CACCTCTCTG GACCCACAAA GTATGCTCAG GCCCAACACT GCCCTCTGCG 540
GGAGCCTGCT TGGCCTCTCC ATTGCTGTGC AAGCGATTTC AGCCTGGCCC AAAGAGCTCC 600
TTCCACCCTG GAGCAGGTGT TTGGGAAGGC TAGGGTGCCT TAGGCACTGG GGACTTCAGC 660
TGGGGGGTGG GGTGGGAGGT GAGCTGCCTT GGGAAACCCC CCACACCCTC ATGTGGCTGG 720
CTGAAGAAAT GCCTCCGAGG CTCCAGCTGA ATGCCGCTCA AGGCTTTTGG AGTTAAAACG 780
GCCCTTCTCA TTCCTGGAGC CTCACCTGCT CCTTGCACAG GTGCCCTGGG AAAACTGTGG 840
GACTTGCCCA AGGTCACTCT GCAGTACAGT CAGGATCAGG ACCCAGCCCA GCTGGCCCTT 900
GGCCATTCTG ACTCCTGCTG TGAGGGTGGG TTGCAATCCA CTGGGCAAAA CACTTTATGC 960
TGGGGCAACA GTGAAAAGTT TGAGCAATAG TGACAGCATA GGATCACCAG GTTCGTCCTG 1020
TTTCCCTCCT 1030
|
