| Tag | Content |
|---|
EnhancerAtlas ID | HS101-12552 | Organism | Homo sapiens | Tissue/cell | HT29 | Coordinate | chr13:52571580-52572570 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXC1 | MA0032.2 | chr13:52572543-52572554 | ATATTTACATA | - | 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 |
| GH13I051995 | chr13 | 52569381 | 52574383 |
| Enhancer Sequence | CACATGCTTT TAAATAATCT ATTCTGTTAG CTCCATGAAA TTGAAATACT TCACCATTCA 60
AACCATTTCT AGATGGTGGC TCAGACCCAG AAGACAGCCA GAAAAGGGGG CTGGGGCCAG 120
GTTAGAAAGG GCAGAGTCTA GACTTTGTCC TGTGGGTGGT GTAGAATCAC CAGGAGTTTC 180
TGAGGAGAGA ACTCACAGAA TCATATTTGT GATCTGGAAA CAGTTTGGGC AGAAACAAGA 240
ATGAAGACCC AGGAGAGGAG GGATTACAAG GGGCAGAAAA TTTAATAGTA GAATACGATT 300
AAACAAACGA GGAGGCCTCC CAACTCAGTG ACTGCTGGAT CACAGCAGGT GACAAAAAGT 360
GGGGGCCTGA GGATGACAAT GCCATTTCCA GTTTCGCAGA TTGAGCACAT GGTGATGAGT 420
ACACCAAGAT GAGCGGGGAG GGTGGGAAGA AGGCAAGTCT GGGGTAAACA CAGTGGCTTC 480
TCCTTTGCTC CCATAGAATC TAAGAGACGT GTGGAACAGC CAAGGCATGG GCCACCTTCC 540
TAGGCTACAG TATTAAGTCC AAACTCCTCT TTCTAGCACC TTCCCCTTTC CTCACACCTG 600
ACCCTGGCTT CCCTGCTCCT CCCCTTCCCG GCACCATCTA ATCCTTCTTA TCCTTTAAGT 660
CCTGCCTCTC TGTGGAATCC TGCTAGCAGC TCTCTCCCTT ATCTGAATTC CAGCATCACT 720
AATGTCAACA TCAGGGTGCC AGCAGGTGGT CAGCCTGTAA CACTGCTGGA GGACAAGTCT 780
TCTCTGTCCA CCGAGGCTGC AGTCAGCTCA GTCCACACTT GTTACTGATG CCTATGGGCA 840
TGTGCTCACT TTGGGAAACG TGGTCAGATC CTGGAACACA AGGATCTCAT ATCTTAGCTG 900
CCCACAGACC TAACATGGTG ATGAACAATA TCAGACATTA AATAAGTATA TTTAAGCAGT 960
TAAATATTTA CATATTTACA TTTGAATAAG 990
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