| Tag | Content |
|---|
EnhancerAtlas ID | HS087-17600 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr6:113885470-113886920 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Hnf4a | MA0114.3 | chr6:113885879-113885895 | AGTGGACTTGGACCTC | - | 6.07 | | NFYA | MA0060.3 | chr6:113885911-113885922 | TCTGATTGGTT | - | 6.62 |
|
| | 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 |
| GH06I113564 | chr6 | 113885401 | 113887461 |
|
Enhancer Sequence | AAGATTTAAG TGATTTTTTT TTTTGCACTT TGAAAATACA TCTTGCTTTA AACACACAAA 60
ATCTTAGCAG CTGGAAGCCT GTTATGTGTT TAATTAAATG GCCCACACAT GTGTTTGTAA 120
TGCACAGCAC TGTGGTCTGT GAACGGAATC CTGGAATCCC CGGGGTGTAT GGTCAGCCTT 180
TTGCCTCACT GAACTCTCCT CTGGAGGCCA TGGGAAACAG GGTACTTGTT TGAGTTTTCT 240
CCTCGGGTCC ACATTTCCTC TATCGACTAC TGCTGTGTAA ACAGACTCAT GTTCAAAAGG 300
TGCTGGGCTC CATTGACCTA ATCCACTCTG AAGTGCCAGA TCTGTCCACA CGTCCTCGGG 360
ATTAGGCCAG CATGGCCAGC TCACCCTGAC TTTGCCTAAG GGATGGTGCA GTGGACTTGG 420
ACCTCCCCCA AGCCAGGTTC ATCTGATTGG TTTCCCTTTT GCGCTCTTCT TCCCCTGGGA 480
GAGGATATCC TCAGCATGGA CTGGGGCCCA CAGAGCATGG AAGCTGAAAC ACCGATTCTT 540
CCTCAATGAG CTGAAGTTCT CCAGATGGCA GCAAGCGCTC GTCATGCAAA TTCTTGGCAG 600
CAGGGAGCCT GTCAAGTGGC TACTGCTGCT TATTGTTACC AACACTCCCC CACCCCCTCC 660
ACACAAATGC AGAAGAAACA CCATCTGTCG CCTGTGGGGC TGAGCGGTTC TTTCCAAGTC 720
CCTTCTAGTC AGTGCCGCTC AGCAGCCCTG CGCTGTGCGC ACGGTCCAAA CAGGAGTTGC 780
CTCTCCTTGA GCCAGGGAGG ACCCCGTCCG GTGCTGGCAG TTCTCTTCTT CCACGCCTCC 840
TGGGCCTGGC CCCTCATCCA GGGCCGAGCC GGGGCGTTTT GCTAGCAGAT TTCTCATAAG 900
ATAGTTATGT AACAAGAATA GGAAAACGAT TGTGTTTCTC CCTTTAGATT CTGGGAAAGA 960
AACAAGATGA ACTGAGTTAG CAACGTGTCT CCATCACTAG TGAGAAATGT GAATAGAAGA 1020
TAACTGGTTA AGGAGCACAC TCCGGATGTG AAAAGCACAG CCTTGAAGTT AAAAGGTCGC 1080
CCATAACATC AGCGTGATTT CGGGTTTGTG TTCTCTTCTC TCCCACTGAT GTTATGTCTC 1140
CTGATTAATG ATGAACTCTC ATAAGACCTA AAAACGTTCT GTACAAACGA AAGCTGTCGC 1200
CAAAAGACTC TAAGCTCTGG AGAAGGCTCA ATATCTTGTC CATCTTTGAA CTCCGAGACC 1260
ATCCGTGCAG TCATTCAATA ACTATTTTTT CTTGTTGTTG CTGTTGGATT TTTGTGGGAT 1320
AGTTATATAT ACAAATACAA ATGCAAGCAA TAATAATATG CCATGTCATA TCTGCGTTTT 1380
TAATGTTTTC TTTTTAACCC CAGAAAGTTG TTCATATGCC TCACCTCAGG TCATTCTATC 1440
TTCCTTTATC 1450
|
