| Tag | Content |
|---|
EnhancerAtlas ID | HS053-08945 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr12:25016900-25018380 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr12:25016949-25016960 | TTTTATTGCTT | - | 6.32 |
| | | 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 |
| GH12I024863 | chr12 | 25016495 | 25018417 |
| Enhancer Sequence | CTGGAATGAT TCCAAATCAG GAGTCGACAA ACTTCAGACT GCTGCCTGTT TTTATTGCTT 60
TTATTGGAAC ATGTTCATTT ATTTATGAAT TGTCTATGGC TGCTTTTGTA CTATAAAAGC 120
AGAGGTGAGT AGCTATATAG CCTACAAAGT CAAAAATATT TACTATTAAG ACCATTACAA 180
AAAAAGTTTG CTAATGCCTT CTCTAAGTGA CAAGAAAATG CTACAGGATG GTTATTATCG 240
CACCAGGAAT GACCTCAAAA CCAAGATCTC CTCACTGGCT CCTGCCTTTG ACCTTGTGGT 300
TATATCCAGT TTGGCTCAGT TGACTAGGCC TCCCACTGTG CTGGCCCTAG AATAGAAAGA 360
CAAAGAAGAC CACAAAGGAT GCTAATATCT GCAATGAAGA TATACCCAAC AACCCCAGCT 420
GAGAAGATGA GGAAGAAGAT ATTGAGTCAA GTAATGAAGA GCTCACACCA AGACACTATG 480
GTGTCAATGG AGCAGTATGT GTGTGACCGT GCAAGGTGGG GGTTGGATGC TGCTCTACTT 540
AGTCACATGT CCCTGCCTGC TTACGTGGTC ACCCTTAGAA GGAGAACTAT GATAGGAATG 600
TGAGAAATCT TTTGAACATT TTAACTATCA GTTTTCCCTT CCTTCTGGCT AATTACTATT 660
AGCTTAGAGA TATGCCATAA TATCTCCCAA CTAAGACACA CACTCCCTTT AGCATCTATC 720
CCATTCCAGG GAGGCGTCCA TTCTCTGTCC CACTGTGCAG CAGAATTCCT CCTGACATTT 780
ATACATATTC AGCATCACAG CTACCCATTC TCTCATTCTC TCTCAAATCC CAAACACTGC 840
AACCCCACCA CCCTACTAAC ACATGCTTAT CAAGATCACC AAGGCCTTCC ACATTGACAA 900
ATCCAATACT CAGTTCTCAG GCCTCATCTC ACTGTGGCAG GATTTGCCAC AGCTGCTTGT 960
GGTTTCCAGG TTCACTTGGT TTCCAGTCCA CTAAACCTCT CTTGTTTTTC TTTCTACCTT 1020
GCAGGCTGCT ACTTCTCAGA CAGCTTAGCA TTTTACAAAC TCCCTTTCTT CTAAATGCTG 1080
ACCTGCCCCA GGGGTTAGTC CTTGCCTTCT TTTCATCTCT ATCTACAGTT CTCCCCTTAA 1140
AGATGTAATC TAGTTTCTCA CCTTCAAAGG CATTTTTATG CTTAAAGACA AGAATCTATC 1200
CCTTAAATTC CAAACTCTCC CCTGAATAAT AGACTTTCAC ATCTATAGTA CCTACATGCA 1260
TGACTGTTTT AACTCTTTAT TCTACCCATA TCACTCCAAC AAACAAACAA AAAAAGACTT 1320
CTTTCTCATT CTTCTCCATC TTAGTAACTG ATTACTATCC AGTTGCCATC GCCCAAAAGG 1380
AAAACAGCAT CTCTTCTCTC ACACCCACAT CCAACCTATC AGCAAATTGT GTGAGCTGCA 1440
GTAAGTATCC TTGAATGTAT GTCTTCACAT GCAACAGGGG 1480
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