| Tag | Content |
|---|
EnhancerAtlas ID | HS043-45100 | Organism | Homo sapiens | Tissue/cell | Fetal_heart | Coordinate | chrX:118868570-118869710 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA | MA0729.1 | chrX:118868719-118868737 | GCTGGAACTTTTGGCCTC | - | 6.06 | | RREB1 | MA0073.1 | chrX:118868887-118868907 | TGTGGGGTGGTGGTGGGGAG | - | 6.23 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TAACCTCAGC TCACTGCAAC CTCCACCTCC CGGGTTCAAG CAATTCTCGT TCCTCAGCCT 60
CCCTAGTAGC TGGGATTACA GACACACAGC ATCACGCCCA GCTAATTGTT GTATTTTTAG 120
TAGAGACGGG GTTTCACTAT GTTGGCCAGG CTGGAACTTT TGGCCTCAAG TGATCTGCTT 180
GCCTTGGCCT CCAAAAGTGC TGGGATCACA GGTGTGAGCC ACCTCACCCA GCCTTTAGCC 240
AGCTTTTGAC GCACAACGAG TGGGGGTAGC AAATTCTTGG GCATGTCCGC TTACAAATGT 300
GGAACCCAAT GTTTCTATGT GGGGTGGTGG TGGGGAGGTG GCTGCTCCTC TAGCAACAGT 360
GATCCAGGCC AGCCCTTGGC AGGACTTCCT CACCAGAGTC GGCTGCAAAG CCAGCCAGCT 420
GGCAGCCGGC CAGGCTCATA GAGTGAACCC ACTTGGAGCC GAGAGCCCCA CAGAGGGCAC 480
AGCAGGGGCA TGAGGTCCAA CAAACTCAGG CTGTGTGTGC TTCTGCCCCA GAGAATACAA 540
CGGCACTGGG AGAGACAGCA GCCACAGCTT CCCGAGAAGC ACTGGAATCC TAGGAGCGGC 600
TGCCGGGCAG GGGCAGGCAA GGCAGACAGA TGGAAGAGTG CCCAGGCTGC ATCATGGTAG 660
CAGTTTGAGG TTCTGTTGAA GGAGGGAAGT GACAAGCTGG GCTGAGTGAC AGGCATGGAT 720
GAGAGGGCAG ACCAGGCTCT GGAGAAAACA GCACATGAAC CCATCTTTAG TGACAGTGAA 780
CTGAGCAGAG AAATGTCACT TTCAGGCCTG GAAATGGCCA GGGAGGCATA ATAGTGACTC 840
CTGCAGGGGG CTTCTCCTCA ACCGGGAGCT GGGCGTCCAG GGCAAGGTGG CCAGGCTTGT 900
GCCATCTCAA CTACTTGGGA ACAAATAGAC TTGGCACTCT ATGTTTAGCC ACCAAAGTCA 960
AGACCAGGAG CCCCGAAGTC CCATCCCCCA AGGAGCTGAG GAGCCCAGAT GCTAGAAAGA 1020
GGGCCACAGG ATGAGCAGGG CCAGCAGCTG CCTGGCAGGA CATCTGTCAC AGCCCATTGG 1080
GCAGCAACCA AGAGGAGTGC GGAGGCTACG CGGCCCCATT TGCTGAAGGG GAGGGCTGCA 1140
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