| Tag | Content |
|---|
EnhancerAtlas ID | HS108-21676 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr2:24123280-24124430 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr2:24123984-24123995 | ATGAGTCATCC | - | 6.62 | | JUNB | MA0490.1 | chr2:24123984-24123995 | ATGAGTCATCC | - | 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 |
| GH02I023900 | chr2 | 24122981 | 24125731 |
|
Enhancer Sequence | TACAGACTCC CAAGGTTAAA GTGTGCATTA AAGGTCATCT AACTGAATTA CTAATCCAAG 60
ACATTCTTTA CTCCAATTCT GGTCTGTGAA CCAACAACAT GGGCATGATC TATTTGGAAG 120
CTCATTAGAA ATGTAGAATC TCAGGCTCCA CCCTCAGATC CACTGAATCA GAAACCATTT 180
TTAAAAGATC CCCAGGTGAT TCATGTGCAC ATTAGAGTTT GAAAAGCATT ATTATATAAC 240
ATATTCAAGA CGTAGTCACT GGACCGCCTG ACTGCCACCA TCATGAGTCG CATGTGCACT 300
CCTGGGAAGG GCCTGTCTCA ATCGGCTCTG CCCTGTCACT GCAAGGTTCC CACTTGGCTG 360
AAGCTGACAT CTGATGACAT GAAGGAGCAG ACTTACAAAC TGACCAAGAA GGGTCTGCCT 420
CCCTCACAAA TCAGTGTGAT CCTGAGGCTC ATATGGTGTT GCACAAGTAT ATTTTTGTGA 480
CAGGCAATAC AATCTTAAGA ATCCTTAAGT CCAAAAGACT TGCGCCTGAT CTCCCTGAGG 540
ATCTCTACTG TTTAATTAAG CAAGCAGTTG CTATTCGAAA GCATGCTGAG AGGAACAGAA 600
AGGATAAGGA TGCCAAATTC CATCTGATTC TGATAGATGA ATTCACCGAC TGGCTCAATA 660
TTATTAATAC AAGACCAAGC AAATCCTCCC ACCCAACTGG AAACATGAGT CATCCACAGC 720
CTCTGCCCTG GTTGCATAAG TTTGTCTACG TACTCAAGTA ATAAAATGAT TGTTTATCGA 780
AAAAAAAGGA GTCACTGAGG AAGCAACATC ATGTATTTTA AGCTAGAGTG TATCTGTGAT 840
ACAGAAACTA GTACCTATAA ACTACTGTAC CAATTTAGAT AGCCCAGGCC AGCATTACTC 900
CTTCCAATCA AATTTGATCA TTCATCTTCA AGACCTATCT CAGGACCCTT TTTTTTTTTT 960
TCTTCATGAA ATCTCCCTGA AGAATCTAGC CTAAATTAAG CTTATCCCTG CTACTAGTTG 1020
CAGCCCTACT ATACATTTGG GCACTTGATT ATTTCAACTT AGCATTATAT ATTTATCATC 1080
TTTAAAGTGT CATGTCCAAG TCTTGAAATT CTAGCAAGAT TTTAAGCTCC TGAATTACAA 1140
AAACGTACCC 1150
|
