| Tag | Content |
|---|
EnhancerAtlas ID | HS043-04240 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr1:231913430-231914810 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HOXA13 | MA0650.2 | chr1:231914510-231914521 | CCCAATAAAAC | + | 6.62 | | KLF5 | MA0599.1 | chr1:231914002-231914012 | GCCCCGCCCC | + | 6.02 | | MEF2A | MA0052.3 | chr1:231913891-231913903 | TCTAAAAATAGA | + | 7.22 | | MEF2C | MA0497.1 | chr1:231913889-231913904 | TATCTAAAAATAGAC | + | 6.68 |
|
| | 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 |
| GH01I231775 | chr1 | 231911245 | 231915153 |
|
Enhancer Sequence | GACCTCCCTG CAGGTGTGCC CTCTCCACTC AAATTTATCC TGTCTGTCCT TCTTAGTTAG 60
ACTGGTGTTG ATACTCATAC ACTAATTTTA ATATCTCTGT TATTTACAAA CTGTCATACT 120
TGCTTACAAT AACCCTATAA GGTTTGTTGG GCAATATATT GTTTTTATGC CCATTTTGCA 180
GATGAGGCTG CTGAGGGTCC AAGTTCACAC AGCCGTAAAA GCAGTGCCCT CACGTCTTTG 240
GCGAATTTTT AATGCAGAGG GAATCCAGAG ATGGTTCACA CTGATGGCCT GGGAGAGACC 300
AGGCCTTGGA CAGAGTGCTT AGTCCAGCAA TGGAAAGAAG TCCAGCCCAG CAGAGCCGTG 360
GGTCTGTGGG CCCAAGGAAA AGAGAATGGA TGTCCCTCCA GGCCAGGGAT GGTTGTCTCT 420
GTGTGCCTAG TGTTGCCTGA TTGGATTGGA GCCAAGGTGT ATCTAAAAAT AGACAGCCTG 480
GGAAGACCAA ACAGGCAACT GTCTCAAGTC AGAGAGGTCT GTCAGACGTT CCAAAGAAAG 540
AAATGTGAGA GGAAGAGAAA CTGGAAAGCA AGGCCCCGCC CCAGGGCTAG AGGAACTGGT 600
ATTACTTGTC TGTGAAAAGA GGGTTTGAAC TGGGTGGCGT GGAAGGTCTT TTCTGGTTCT 660
ACAATACTTT GCACTTTAGT ATTTTATGAA ATAAGTTAAA ATAAGCTGCC TAAAAACCCC 720
TCATAATTCT ATTCCTAGGA GCTCTATGTT AAGTTCCTCC TTAAAGTTCC CTGGGCAGGC 780
TGTGACCATC CACAGGCCAC GGTGCTCCAG CTGGCACTTT CCTTAGGGCT GGTCCCTAGA 840
GCATGGACCT GAGCAAAGCC TGCTTTCCAA GCACTGCTGC TGCAGCTCAG AGCTTAGACC 900
TCGCCTCACC ATTGTATATC CTCCCGTTTT CTTCTGGAAA GTCGTCATTA CAGGCAACGT 960
GGAAAAGTTT ACCAGACTAT AATCTGGTAA AGGAGGAAGA GGATTGGAAA AGAAGGAAGA 1020
GATTTGAAAA TCCCCCTTAT CTGGCTGGGT ACAGATGCTG CTCACCAGGA AATGTAGGTT 1080
CCCAATAAAA CAGGACCCCC ATTTCCAGTT TTCATTGCGT TGTAAATTAA AAATAAAATC 1140
TTAAGCCCCC AACCACTGAA CGGATTCCCT CTTGGCCAAG GAGACCCCAG AGACTCCATA 1200
CAAACTGAGT TCCCAGCCCC AGTGGGCCGG GAGGTCGGAT TTGCCTTGTT ATAATCCCTC 1260
CCTTTTGTAG CTTAGACATA ACAACAGAGC AGCATCAATG CTAAAACGAG ATCATAAGAA 1320
CTGATGGAAC AGACTCTCGG TGGCAATAAG ATACCAAATT ATAAACAAGA CCTAAGGCCA 1380
|
