| Tag | Content |
|---|
EnhancerAtlas ID | HS098-29185 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:24658120-24659520 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MIXL1 | MA0662.1 | chr2:24658558-24658568 | TCTAATTAAC | + | 6.02 | | Myog | MA0500.1 | chr2:24659041-24659052 | GACAGCTGCAG | + | 6.62 | | Tcf12 | MA0521.1 | chr2:24659041-24659052 | GACAGCTGCAG | + | 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 |
| GH02I024433 | chr2 | 24656789 | 24659939 |
|
Enhancer Sequence | GAAGCTGGCC TAGGGTCCCG ACAGGAGTTG TCTCACACTC CGTCCCACGG AACTGGGGGT 60
GAGGTGGTGG CAGTGCTGGC ATCAGACCAT AACATAAAGG GAGTAGCTGA AGCCCTCCGA 120
AGTAGGCCAC GCCTGCGCCA TTGCACAGTT CGGAGCTCTC CCATCAGCCC TTCCGAGTGC 180
ACTGCCTCAA GTCGCACATC CAAAGTGAAA TGTGGGTGTT TTAATCACTG AAGAGAATCC 240
TTAATGCTGC TCCTTCAGCA CATAGCTGTC TCTCCTGTGC CAGGAACCGC AGGGAGCCTA 300
TTGCTTTCCA TCCTGAACTG GATCCAGAAG CGTTAGGTGA GGCTCAATAC AATTTTCAGT 360
TGTTATCATG GGAGGCCCTT AGAGACGCTT CTCAGTTCTA GCAATTAGCC ACACAGGGGT 420
CAACCAAGTG TTCTCAGCTC TAATTAACAG CTGTGTTGAA TCTGGGACAC ATAGAATTCC 480
TTTGGGGACG CACTCTTCAA ACAGAAACAA AGCCAGAATA GCAAGCTCTT TCCTCCTTAT 540
CAGAGGCTAT GAAGTATGAA AATGACTGCT GAGGGGATTC TTAATGAAAA TACCGGGAAG 600
CTGAGTGGCC TCCGGGCTGC ATGTATGAAT TTAAAGGCAA AAAGACAATC TCAGCTTGAC 660
TATGAAGTTA TCTGCTGGGG CTCAGGAGGC TCTGGGGAGC GCTGGGGGAA TTAGGTGCCT 720
CTTAGCTCCA CTCCCAGAGC CCGGTACACC CAGCAGGCTA CATGATAATC ATCACCACAC 780
AAATCAAAGG CTTGATCTCT GGCTTCAAAA GGAAAAGGAA CAGGAACAGG ATACTCTCTG 840
TTGGGACTCC TGCTCTGAGC GGGAACTATG CTGATGCCTG TTCAAGTTGT TCCCTGGGTA 900
TTTTGGCTTC TTGCCCTGCC TGACAGCTGC AGGAGTTCTG TAAGAAATCT GAGGGAGAAT 960
TTCCTTTGCA ACCATGACTG AGAACCCAGG ATCAAGAGCT TTGCAGACAG AAAAGACATT 1020
ACCCTTCGAA TATCCCAAGC CATCTATTAG GGTCAGCAAG CAGCCGGCAA AAAGCGGGGC 1080
AGCTGGTGGT CCAGCCCTGG GTGGAGAAAG TGGATTCCAT CGGGAAACAG CCAGTTGAAG 1140
TTTTCTTTAC TAACTGAGAG CAAATGCACC GAGGCATTTA AAAATAAGCA TATGTTCATA 1200
CTGGAATATT TCAAATGAAC AGAAACAACA CCTAAGGCCC AGATCGATAA ATATTAACTT 1260
TGTGACACAT TTACTTCACA ACTTTTTCTA AACAATTTGG TATACATTAA AACCTACCCC 1320
TTCTTCCCCT GGCTCCACTC CCCACTCCCA TCCTGAAGTT AGTAGGTATT TTTCTATGTA 1380
AACCACAACC AGGGGTTTAT 1400
|
