| Tag | Content |
|---|
EnhancerAtlas ID | HS053-01440 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:53130300-53132840 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr1:53131473-53131490 | TGGTACATGGTGTTCCC | + | 7.19 | | Ar | MA0007.3 | chr1:53131473-53131490 | TGGTACATGGTGTTCCC | - | 7.37 | | Lhx3 | MA0135.1 | chr1:53132127-53132140 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr1:53132131-53132144 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr1:53132124-53132137 | AATTAATTAATTA | - | 6.78 | | Lhx3 | MA0135.1 | chr1:53132128-53132141 | AATTAATTAATTA | - | 6.78 | | Lhx3 | MA0135.1 | chr1:53132132-53132145 | AATTAATTAATTA | - | 6.78 | | Lhx3 | MA0135.1 | chr1:53132123-53132136 | AAATTAATTAATT | + | 6.92 | | Lhx3 | MA0135.1 | chr1:53132135-53132148 | TAATTAATTAAAT | + | 6 | | NR3C1 | MA0113.3 | chr1:53131473-53131490 | TGGTACATGGTGTTCCC | - | 7.3 | | NR3C1 | MA0113.3 | chr1:53131473-53131490 | TGGTACATGGTGTTCCC | + | 7.49 | | NR3C2 | MA0727.1 | chr1:53131473-53131490 | TGGTACATGGTGTTCCC | - | 7.1 | | NR3C2 | MA0727.1 | chr1:53131473-53131490 | TGGTACATGGTGTTCCC | + | 7.27 | | POU6F1 | MA0628.1 | chr1:53132125-53132135 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr1:53132129-53132139 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr1:53132133-53132143 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr1:53132125-53132135 | ATTAATTAAT | - | 6.02 | | POU6F1 | MA0628.1 | chr1:53132129-53132139 | ATTAATTAAT | - | 6.02 | | POU6F1 | MA0628.1 | chr1:53132133-53132143 | ATTAATTAAT | - | 6.02 | | ZIC1 | MA0696.1 | chr1:53132186-53132200 | CACCACCTGCTGTG | + | 6.04 | | ZNF263 | MA0528.1 | chr1:53131373-53131394 | CCCACCTCCCTCCCATCCTTC | - | 6.72 | | ZNF740 | MA0753.2 | chr1:53131405-53131418 | CATCCCCCCCCAC | + | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 53130725 | 53131970 | | chr1 | 53132148 | 53132298 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I052664 | chr1 | 53130630 | 53131956 |
|
Enhancer Sequence | GATTGCAGGC GTGAGCCACC GCGCTCGGCC CTGATTTTTT GTATTTTTTA GGAGAGACGG 60
GGTTTCACTG TGTTGGCCAG GATGGTCTCC ATCTCCTGAC CTCGTGATCC GCCTGCCTCG 120
GCCTCCCAAA GTGCTGGGAT TACAGGCATG AGCCGCTGCA CCCCGGCTAT TTTTATTCTA 180
AGACAGGATC TTGCTCTGTG CCCAGTCTGG AGTGCAGTGG TGCAATCATG GCTCACTGCA 240
GTCTTGACCT CCCTGGCATA AGTGATCCTC CTGCCTCAGC CTTCTGAGTA GTTGGGACTA 300
CAGGCGCACA CCACCACGCC TAGCTAATTT TTGTATTTTT AGTAGAGACG AGGTTTTGCC 360
AAGTTGCCCA GGCTGGTCTC GAACTCCCAG GCTCAAGCAA TCCGCCAGCC AGCCCATTTT 420
GATCTGCACA ATACTTAAGC TGAAGGTATA ATACCACCCA CCCCTATGCG ATGTCTGTAC 480
AGATGTGAAA GGACTTTGGA AGTTGTGATG TGCTCGACAG ATGTTATTTA TTGTTACTAA 540
ATGAAAGTTG GGGAAAGATC TCCTAGATTT CTTCCCAAGG GGCTCCAATT GTCAGACTGT 600
TCAATTCTGA AATTTTCTAT TGTTAACATA TGTGGTGCTA AAGGTCTGTA ATTGTGGAAT 660
CTTGAGCCTG ATTCTAATCC TGTGAAACCA GAATCCTGTG AATCTGACAT TCTGTAACTC 720
TATCCAAGTG GGAGGTCAAG GTCTGAAGGC CAGGGCAGGG TGGGGACAGA GGTCAGCAGG 780
AGGATCCCAC TCCCCTAGGG AGGAGCAGTT GTCCCCGATG TCTTCTACCT GGGCTCACCC 840
TTGGAGCTAC AGCCTCATTA TCATTCAGAC TTATCATGAG CTCATCACCC TTCCTCCAAC 900
CAGCCCTCCC TGGGGCCTCA TTGTATGCAT TATCCATATT CATTACACAT TTTTCTTCCA 960
TTAAGTCGAA TTAAGCCACT TTGCCAACAC TGCAGGAACC AAAATCTCCC TCAATAAGTA 1020
TGGGCCCTAT TGGGGCCCAG AGGAGGCCCT AAGTTAGGAC AAATCTACCC ATCCCCACCT 1080
CCCTCCCATC CTTCTTCTCA AGCACCATCC CCCCCCACTT CCCTGTACCC CAGATCACAT 1140
GGAAGCTGCA GAAGCACTCC TTTCTGCAAG TTCTGGTACA TGGTGTTCCC TCCCTGATGG 1200
CCTCACAGGC AGCTGCTGAC TCACCCCAGG TTGCTAATGC ATCAGGTAGC CATGTATTCC 1260
GATGGAGCTG CTTCATAAAA TGTAGCAGCG TGTGCATGTG TGAGCTCACA TGTGTGAACA 1320
TGACCAGAGC ACCGGCCCTG GGCTGTGGAC TTGAGACCTG GATTCTAGGC CACCACTATT 1380
TACAGGGTTA CCTTGAGCTA ATGCCTTCCT CTCTGTCTCA AGAGAATATC CCAGCCCTTC 1440
TGGCCTCACT AGGTTGTTTG GATACTTACG AAGAAATGTG TTAATAATAC ATTGTTCTAC 1500
AATGTGTTAT GAAGTAAAGT GATATCTAAA TGCAGTGTAC CGGCTGGGAG CGGTGGCTCA 1560
CGCCTGTAAT CCTAACACTT TGGACGACTG AGACGGGGGG ATCACTTGAG GTCCGGAGTT 1620
CAAGACCAGC CTGGACAACA TGATGAAACC GTGCCTCTAC TAAAAGTACA AAAATTAGCT 1680
GGGCGTGGTG GCAGGCGCCT GTAGTCCCAG CTACTTGGGA GGCTGAGGCA GGAGAATCAC 1740
TTGAACCCAG GAGGCGGAGG TTGCAGTGAG CCAAGATTGC GCCGCTGCAC TCCAGCCTGG 1800
GCAACAGAGT GAGATTCTGT CTCAAATTAA TTAATTAATT AATTAAATGC AGTGTACCAC 1860
CAAGATGTCC ATGTCCAGCC CCATAGCACC ACCTGCTGTG TGACCTTAGG CAGATCATTT 1920
TACTTCTCTG AACTTTTGTT TCTGTGCACA CGCGCGTGTG TGTGTGTGTG TGTCTATAGT 1980
TTTTTGAGTG CTTACTATAT GCTGAGCATT GTGTCTGGCA TGTTATGGGG TTTACGCTGT 2040
ACCAGTCAAG ATTCTCAGTT GTAAACAAAT TCTCAGAGGT AGTTGCCAGA AACTACCTCT 2100
GGCAAAATTA AGCAAAAAGG GTCTTTACTG GAAAGCTATT GGATGTCTCA CTGAAATGAC 2160
AGGGAGACCA CAAAGCTAGA TGAGAATCAA GGGCAGCTGG GCACGGCCAA AGTCCTGCCA 2220
TGGGAACTAT GTGTTTAGGA CAGACTCTGC CTCTAGCCAC ACAGATACTT GCTGATCACC 2280
ACTGCACTGC TAGGCTCTTG CCCCATTGCA GCCACCTGAA GTAATCTCTG TCCTTGCCCC 2340
TCTGCTAACT GCCACCAGAC TCAGCCCATG TAGGGCATTG ACTTGGCCAA TCACAAGCCC 2400
ACAAGGGTCA GGAGGAGTTG CTGCCTCCTT CAGCTCCCAC ATAGCTTGGA ATTCCTCCAG 2460
ATAGGGAGTG TTTGGATGCT GGGTGGCCCA GAGCAATCAA TGTCCACTAT AGGCTTCACC 2520
AATTCTGAGT TTGGTAATAT 2540
|
