| Tag | Content |
|---|
EnhancerAtlas ID | HS053-22000 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr2:132426010-132427760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr2:132426323-132426335 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr2:132426327-132426339 | AAACAAACAAAC | - | 6.32 | | TP53 | MA0106.3 | chr2:132426672-132426690 | GGCTTGCTCAGGCATGTC | + | 6.37 | | TP53 | MA0106.3 | chr2:132426672-132426690 | GGCTTGCTCAGGCATGTC | - | 6.5 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 132426365 | 132426830 | | chr2 | 132426834 | 132427227 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I131667 | chr2 | 132425552 | 132428164 |
|
Enhancer Sequence | ATAAAACAAA ATTACTGGCC AGGCACAGTG TCTCATGCCT GTAATCCTAG CACTTTGGAA 60
GGCTGAGACT GGTAAATCTC TTGAGCTCAG GAATTTGAGA CCAGCCTGAG CTCAGTGAGA 120
CAGTGAGACC TCGTCTCTGG AAAAAATACA AAAATTAGCC AGCGATAGTG GTGTACACCT 180
GTAGTCCTAA GTTACCTGGG AAGCTAAGGT GGGAGGGTGG CTTGAGCCCA GGAAGTGGCT 240
GCAGTGAGCT GTGATTGCAC CACTGCACTC CAGCCTGGGT GAAAAAGCCA GACCCAGTCT 300
CATACAAAAA TAAAAACAAA CAAACAAACA AAAAAGTTAT TACTTAAGTC TCACATGCTG 360
TCTTGGAGCC ATCTTAGTGT TGAGGGATTC AAGAGACTGG AGAGACCAAT GGGTGAGACA 420
GGAGGATTTT ATTAAAGTGA CCACTTGCCC AGTGGATTTG CATCCAAAAG GCTGAGCCCG 480
GAAAAAAGAC GGGGCCTGGT TTTTAAGCAT GCAGCTGTGC AAAACTTACA GGGCGGGCTT 540
AGCAAGCTTA CAGAAGCAGA ACAAAGGCAG TTAATCAAAC AGTGACAAGT GTATGACTCA 600
AACATGTCTG ATGACCTCTG CTGGGCCACC CAGCAGGCTC TCAGCAGATG GTAACTATTT 660
TAGGCTTGCT CAGGCATGTC TTGTGACCTT CTCAGGGTCA CACAGATGGA AAACAGGAAC 720
TTAAAAAATC CTTATAAACT TACAGAGATA GTTACAAAAA TAGTTATGAG AGCAGAACAA 780
AGAAATATTG GCCTGGGAAA GAATCTCAAA GGGGGAAGCT GATAAGAACT TGTTTTTCTC 840
ATCCCTGTTC CTGGAGTCCA TTCCTTCTGG GCTCTTCCTG GCCTTGTATA TAAAGTTATC 900
TTAATTCTAG CACGGCCTTG GAGTGAGTCA GCCTGGAACA GGCAGGAACT TAGGTTTTTC 960
TCTTTTTAAT TTCTGCTTTA GTAGGCCAGG GTTCTGATTT TCACTGCTGA GAAAGTAAAG 1020
TGTGTTCAGG CTGCCCATGG TTCTGGGCCC CCCCGGGTCT CTGAGGAGGG CTGTCCCCTC 1080
CATCACAGAG AATATCAGGA CACTAGCTTG TTCTAGTTAT ACTTACACAC TCCTCTCATG 1140
TTGTCTATGG AGTGGTGGAT GCTGCAGGGA GGGTGACATC CTAGTTAGTC CTAAGAGCCA 1200
GACTGCCTGA AGCTCACTAT AACAAGTCCT GCCTTGGGGA AGAAGGAAGT GTGTCTCTGT 1260
GAACCTCCCA CCTGGGCCGA AGGGAGGCCA CTCTCTCTGC TGCCTCTCCC CAACCTTGGC 1320
CTTCTGTGCT CCTAGTGAAC CTCTCACCCC CTGCCTACAG GCCTCGAATC TCAAGACCAT 1380
GATGACCTCT GGTCACCCCT GAATCCAGAG CTTTCCTTTT ACAAAGGGGA AACTGAGACC 1440
TGGAGCAGGG CTGATGTTCA GCCAGCGCAC AACGGAATGG CCGAATTGGT GGTAAAATAC 1500
TGAAATAGTT CCAGTGTGGA TGGAAAGGGG CTGCTGCCCT AAGCATCTCT ACTGCCCACC 1560
TCATCCCTTC CTCCAGGACC CTGGGTCAGC ACCAGGAGCA TCAAAGTGGC CAGGATTGGC 1620
CGGAGCCCAT GCTAATGGCT CTGCCAGCCC TTCTCCCCAC CAGAGAGGGC AGGGGGATTC 1680
AGGCCATCTA GAGGTAGCAT TGTGACCGTA TCTGCAGTAG TCAATCCTTG TGTGCCACGG 1740
TCCCTGACTT 1750
|
