| Tag | Content |
|---|
EnhancerAtlas ID | HS091-08382 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:77380620-77382050 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr11:77380838-77380854 | CAATATGTAAACAAAT | + | 6.15 | | FOXP2 | MA0593.1 | chr11:77380842-77380853 | ATGTAAACAAA | + | 6.14 |
|
| | 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 |
| GH11I077669 | chr11 | 77380829 | 77381955 |
|
Enhancer Sequence | AAAAATTCAG TTCCATGGTC ACACTAGCCA CATTTCAAGT GCTCAATAGC CATATGAGGT 60
TAGTGGCTAT TGTAACGATC AGCACACATA TAATCAGTGC AGAAAGTTTA ACTGCACAGC 120
ACTATTTATC ATCAGAGGTT AGCACATTTT TTATGTAAGA GGCAGGCCCT ATAGTCTCAG 180
TCACAACAAC TCAGCTTTTT GAGAAAGCAG GCAACAGACA ATATGTAAAC AAATTGGTAT 240
GGTAATCTTC CAGTAAAAAC TGTATTACAG GGCAGGGTGC AGTGGCTTAC ACCTGTAATC 300
CTAACACTGT GGGAGGCCAA GGTAGGGGGG ATCACTTGAG GCCAGGAGTT TAAGGTCAGC 360
CAGGGCAACA CTGCAAGATC TCATCTCTAT AAAATAAATT TAAAAATTAG CAGTGTGGTG 420
GCTTATGCCA CTTCTAGCCA CTTGGGAGGC TGAGGCAGGT GGACTGCTTG AGCACAGCAG 480
ATTGAGGCTA TGGTGAGCTG TGATTGTGCC ACTGCACGCC AGCCAGGGTG AGACCCTGTC 540
TCAAAAACAA AAACAAAAAC CTTGCTTTTT TATTTATGTA AGCAGGTGGG CTCTCGTTTG 600
CTGACTGGCC CCCACTGACT TCTTTGCTTC ATCTCATTAT GTCTGCCTTC ACTCATTCTG 660
CTCCAACAAC CCTGCACTCC CTTCTGTTTG CTGAACATGA CAAGCACAAA CATACCTCAA 720
GGCCTTCATA TTTATTGTTC CATCTGCCTG TATCATTCTT CTTTTAGATA AGTGCATGAC 780
TCACACACAA CATTTCTTTC AGGTCTTCAC TCAAATGTTT TCTTAGTGAG GATTTCCTTA 840
GTATATTATC TGAAATTCAA CTACTTTCCC AACCCCCTTT TCTCCTTTAT TTTTTTCCAA 900
AGCACTCATT TCTAATATAT CATATATTCT ACTTATCTAT CTTGTTTATT GTCACCTTCT 960
TCCCAACTAA AATAAGAGTT TCATAAGAGC TATTTTGTTT GCTGTTATAT TCCAGTGCTT 1020
GGAATAGGGC CTAGCTTAAT AAATATTCAT ATTTAATGGC TTAACTAATG CAATTTATGT 1080
TTGTTTCTGT GACACATGAA GGTAAGTACA CATTCGAAAA AGATGTTCAC TTCCCTTCTT 1140
TAGCATCCCA CATCCAAACA TTTTTTTTCC CTTTCTCTTT TGTCTTGGGC TCAAACTTAA 1200
ATTCATGTTT AATCTATGAA AGCAAAACAA TCTTCAAAAC AGGCCATAAA GCCGGGCGCG 1260
GTGGCTCACG CCTGTAATCC CAGCACTTTG GGAGGCCAAG GTGGGCGGAT AACCTGAGGT 1320
CAGGAGTTCG AGACTAGCTT GGCCAACATG GTGAAACCCC ATCTCTACTA AAAATACAAA 1380
AATTAGCCAG GCTTGGTGGC ACATGCCTAA AATCCTAGCT ATTGGGAGGC 1430
|
