| Tag | Content |
|---|
EnhancerAtlas ID | HS052-33537 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr6:130341240-130342710 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MNX1 | MA0707.1 | chr6:130341573-130341583 | TTTAATTACC | - | 6.02 | | ZBTB18 | MA0698.1 | chr6:130342477-130342490 | CAGCCAGATGTTG | + | 6.25 | | ZNF263 | MA0528.1 | chr6:130341866-130341887 | TCCTTTTCCTCCCCCTCCCCG | - | 6.21 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAGGAAAAGA GGGGTCGGGG CCGGGGCCGG CGCCGGGGCC ACCGCCCGCC TCGCGCCGCG 60
TGTGTGTGCG GTTCCGGAAT AATGGGCTTT GCACACTCGC GTCCTGGGCC CCGCGGGCCG 120
TCCTCGCGCC GCGGCGGCGG GGCGGGGGGA AGTAGAGGCC GGCGGGGGTG GGGATCGGGA 180
AGCGCAGGAG CCGAGGCATC CGCCGCGCGC CCCGCGAGCT GGTGGAGTGT GGGGGCCGCC 240
GGGCGGGGAG AAAAACTTGA GAGCCCTGGA AGGGGAGGAG GGCACGGTGG CACGGGCGGG 300
GGGAGGGCGC AACTTTTGGA CTGGTGGTAA AACTTTAATT ACCTTTAAAG AAAAAAAGGC 360
CCTGCGATTC CCCCCTCCCC CAGTCCCGGT CAAAGCACAG CCCGCAGCGC GACCGTGAGA 420
GAAAGTTTAA AAGCGGGCGT GTTCCTCCCG GGTCCCCGCG GAGGGCTGGG GGCGTCGGTC 480
TGTCCGTCGC GCTCAGAGGG AGGTGGGGGT AACTAGCCGC TTTCCAGGGC GCGGGGACCG 540
CGGCTCTACC CCACCCTTCC ACGGGAGACG GAGGTAAACG TTGCTTCGGT TTCCCTTCTG 600
AGTCCCCCTG CTGCCACCAC CCCGCTTCCT TTTCCTCCCC CTCCCCGCCG ATTTTTTGAG 660
GGGACCCGAA AAACGGAGTC CCTTTCCTTA GGCAACTTCC TCGGGCGCTG TGAGCACGGC 720
CCTCCCCCTC ACCGCCCCCA CCCCCAACGC CTCGCATCCC TTGGCCCGCT TCTCCACCTC 780
GGGGCCACCG CCAGAAAAAT GCATTCGAGA TCATTCAGAG TGCACAGAAA CAAAAATAGA 840
TTTTTAATTG TTAGGTTAGG GGAAACTGAG ATGAGAAATA AGAATTTGGG GTGGGGGGGC 900
GCGGCCGGGG CGAGTGCGTC CAGTTCTCCT TTTGGTTTTC CTAGAGCGTT GTTTGTGATG 960
TCTTTATTGG TTTAGGGAGT CCGAGAGGCT CTATGCTGGC TATCTCGGTC GCGTGGATTT 1020
TTGCGCAAGT TTTTAGAAAA ACACTGACTC GAGTAGAGAG CATTTCTCCG GAAAGTTTCA 1080
AGTGCAGCAA AATAGCGAAC GTGCAAAACT GGCCAAGGGG AGACCTCTAG TGGTTGAACG 1140
CGTCTTTTAA GTTCGGAAGG CCGAGAGCAA AGTTTGGCCT TTACTCGTAG CTACGTAGTC 1200
CGTTCAGACG TGGAAGTAAT TAGAGGACCT GAGCGAGCAG CCAGATGTTG TGTGAAAGGA 1260
TGCTGATCAG AAATTGAAAG TTTAGTAAAT CGAAGCAATG AATTCTGAGG ACTCAGACCC 1320
TGTAACTTCC ATCCGACATG AGTTATATGG GAAAGACACT TTGCTTTTAT TCAGAGATTT 1380
GAGATTGATC GCTCCCTGAA TTGGAAACAA TTGTTTGCTT TTGCATTTAT CGGTGTCTGT 1440
ACCTCTGATC AATTTTTAAT TAACGAGTCT 1470
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