| Tag | Content |
|---|
EnhancerAtlas ID | HS053-27771 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr3:122112400-122113910 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT1 | MA0137.3 | chr3:122112668-122112679 | TTTCCAGGAAA | + | 6.62 | | TP53 | MA0106.3 | chr3:122113205-122113223 | GACATGCCCCAACATGCA | + | 6.31 | | TP53 | MA0106.3 | chr3:122113205-122113223 | GACATGCCCCAACATGCA | - | 6.53 | | TP63 | MA0525.2 | chr3:122113205-122113223 | GACATGCCCCAACATGCA | - | 6.49 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAGAATTGTT ACTATTTGAC TTGTCTGACA GTTCGCTGGA AACCCCACTC ACAGGGCTTA 60
TCTTTTTTCA CCTGACTTGG AGTTTATTCA CTGCAAACAG TGTTTTCCCT GGTGCATTTG 120
TTGAAAATAA TCAGCAGCAC TTGTTTGACA TAACATGGAG TGGGTAACAG CTGGGTCAAA 180
CAAGAAGCTG GGGAATGAGA TGTCCATCCT GACATCTGGA AAGCTCTGAC ATATTTCTAG 240
AATGTAATAT GTGTAAGGTT GGACACATTT TCCAGGAAAA ACCTGAGAGG TCTCTAAGCT 300
CTCACCTCAC ATTTAGTCTC TGTCCGAGCA CGAATGGAAG GTGTGTTAGG CCAGTCTCGC 360
ATTGCTAAAA AGAAATACCT ACGACTAGGT AATTTATAAA GAAAAGCAGT TTAATTGGTT 420
CATCGTTCTT CAGGCTGTAC AGGAAACATG ATACTGGCAT TTGTCAAGTT TCTAGGGAGG 480
CCTTAGGAAA CTTACAATCA TGGTGGAAGG CGAAGGGGGA GCTGGCATGT CACATGTCCA 540
GAGCAAGAGC AAGAGAGATC AGGGAGGTGC CACACACTTT TAAACGACCA GATCTCATAA 600
GAACTCACTA TCACGAGGAC AGCACCAAGA AGGATGGTGC TAAACTATTC ATGAGAAATC 660
CACCCCCATG ATCCACTCAC TTCCCACCAG GCCACACCTC CAACACTGGG GGTTACATTT 720
CAACATGAGA TTTGGGTGGG GGTACAGATC CAAACTATAT CAGAAGGCTA AGGCAGTGTT 780
GCAGACTGCC TGCCTGAGGG TAGAAGACAT GCCCCAACAT GCACACACAG CCCGTAGGCA 840
AACACTTAAT AAACTTAAAG GCATTTATTA GTCTCTCCAG TTACTAGCTG ACCACTAAGA 900
TAACCAGACA GACCTCTGTG GCCAAACACA CAAAGGATAC AAGGAGAGAC TATGAACAAC 960
TCTATGGCAA AAATTACATA AACCAGATGA AATGGACACA CTTTTAGAAA AAGAAAAATT 1020
ATCAAAACTA AGTCAAGAAA AAATAAAATA TCTGAAAAGT CCTGTAACAG GAGATTGAAC 1080
TAGTGATTTT AAAACTTCCT GCAAAGAAAA AGTCCAGGCC CAGATGGCTT CAATTGTGCA 1140
TTCTACCAAA CATTTAAAGA AAAAAATAGA ATTAATCTTT CACAAATTCT TCCAAAATAC 1200
AAAAGAGGAG GGATCACTTC CCAATACATT TGATGAGGCC ACATTATCCT CATACCAAAC 1260
CCCTCCCAAA AAAATCTCAA GAAAACTATA GACCCATATA TATCCCTTAG GAATATTGAT 1320
GCAGAAATCC TCAAGAACTG CTACAAAATG AATCCAGTGA CATGAAAAAT TATAGACTGA 1380
TCAAGTGGGA TGTATGCTAA AAATGTAAGG TTAGGACTCC TGACTCAACA TCATTCACCA 1440
TGTTAATAGA ATAAAGGAAA AAAACACATA ACCACATCAG TAAACACAGA AAAAGCATTT 1500
GACAAAATGC 1510
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