| Tag | Content |
|---|
EnhancerAtlas ID | HS007-09369 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr2:166331250-166332680 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ALX3 | MA0634.1 | chr2:166331725-166331735 | TCTAATTAAA | + | 6.02 | | ONECUT1 | MA0679.1 | chr2:166331596-166331610 | GAAAAATCAATATT | + | 6.76 | | ONECUT2 | MA0756.1 | chr2:166331596-166331610 | GAAAAATCAATATT | + | 6.75 | | ONECUT3 | MA0757.1 | chr2:166331596-166331610 | GAAAAATCAATATT | + | 6.92 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CATGGAGGTG AAAAAGCATG GTGTGGCCAG ATGGTCTCTG ATGCATAACA ACACAGGGAT 60
TTTAGAGTTG CATAGAACTC TCCACTTCAG ACCTGCCCCT GATATCCAGT GAGCCTAGTG 120
GCTTTGACCT ACTATCACAG TCTCCTTGAC TTTTTTAGTT TGCTGTCACT GTCAAAATGC 180
ATTTCAGCTT TGTATTTTAG CAAGTGTGGA TACAGTTAGT TGCTGTCATG TTGTGGATAT 240
ATCACAATAT ATTTAATAAT GAAACAAATA GTTTCCTAAA CAGGAGCCCT GAATGTATTT 300
ACAAAGATTT TCATTTGCTT TTCTCTCCTC AGGTTAGGCT AGCCATGAAA AATCAATATT 360
TGTCATCAGT CATTACCAGG TAATACTGGT TGTGATGGTG TCAGCGTTTT AAAGCAGAAA 420
GATTCTGGAA AAGGGTTTCA AAAGTGATTT AAAAAAAAAA GACGTCTTTG TTCTGTCTAA 480
TTAAAATTCC CTTCTCGTTG CTCATGAAAC TCATACTTAA AATTTTAAAT GATTTGCCCC 540
CTGTGCATCC AAATCAATAA GGGCCCCAAG GGGCTGCTCT CATGCTGCCC ACTGAACTTA 600
CCTAGAGCTG AGTGTTAAAT GGAAAACTGA TCTTGGGGAT GCCATTATAA TCCATTTTCA 660
GAGATCTTCC CACAACATAC AGGCAGGGCC AAGGAGAGAA GCCGTGGGCC TGTCCTGTGC 720
TCCCTGCCAG AGCTTCTTGG TGTGTGGTCA TGACAGCCAC TTTGTGATCT CTCAGTACCC 780
TTTCGCTCAC TATCTAAATT ATAGCTCTTG ATGACAAGGA GTTTCCTTCA TCTCTGCATC 840
AATGCCTAAT ACAATGCCTG ATACACAGTA TGTGCCCCCA GATTGTTTTG CCGATTGAAT 900
AATTAAGCAA ATTGTCTTGT CAGATAGTCA TCTAGCCTCC TCTTACATCC TCTCAATGGC 960
AGACACTCCT TACATTCTAA GACGGTCTCT TCCTTCCATG TTCTTCTCTG TTAATGCTAT 1020
TCAGTGTGAC AATGTCCATG TCACCTAAAT GTCATTAAGC CATGCAAGGT TTTGTCTTGC 1080
AGACTTTTTA TTGTCCAAAC GCTATCTGTG CTCTCCTACA TTAACGGGAT TTTATCTGCA 1140
TGTAGTTCCC ATTTCATGCT TCCCTGCTCT GTTTCATTAT AATACTGCTT GGTTTCTGAT 1200
ACACACACAC AGATTATCAT ATACTAAATC AATGGGTTAA TTGTAAATTA ATGTAATTAA 1260
CTGTAATTGT TATATTAATA TATAATACAA GTGTTAATTA ATGTTTGTGT AAGAAAATAT 1320
AGTAGTATAT ATTTAACCAA TCTGAGTGCT ATCATACATC CACTCTTAGT CAATGAATCC 1380
CCATTCTCCT GAGTTAAATT TGTTCAACAA CATTTGATTA AAGTTAAAAT 1430
|
| |
|
|
|
