| Tag | Content |
|---|
EnhancerAtlas ID | HS113-01100 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr1:46022520-46023760 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr1:46022589-46022600 | AGTGACTCATG | + | 6.14 | | Nr2f6(var.2) | MA0728.1 | chr1:46022645-46022660 | GAGGTCAGGAGTTCA | + | 6.22 | | RARA | MA0729.1 | chr1:46023287-46023305 | GAGGCCAACAGGTCATTG | + | 6.63 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I045556 | chr1 | 46022501 | 46022650 | | GH01I045557 | chr1 | 46022945 | 46023870 |
|
Enhancer Sequence | CCTGGGCAAG AAGAGTGAAA CTCCATCTCA AACAAAATAA ATAAATAAAG TAAAAGATAG 60
GCTGGGCACA GTGACTCATG CCTGTAATCC CAGCACTTTG AAAAGCTGAG ACTGGTGGAT 120
CACCTGAGGT CAGGAGTTCA AGACCAGCCT GGCCAACATG GTGAAACCCT GTCTCTACTA 180
ATAATACAAA AATTAGCTGG GCGTGGTGGC ACATGCCTGT AATCCCAGCT ACTGGGGAGG 240
CTGAGGCAGG AGAATCGCTT GAACCCAGGA GGTGGAGGTT GCAGTGAGCC AAGATCGCGC 300
CATTGCACCC CAGCCTGGGT GACAAGAATG AAACTCTATC TCAAAAAAAT AAAAATAAAA 360
AAGATAACAT GAGGGTTTCT GAATGCTGCC AAAGGTCCAG ATAGGCAGTT CCTGACAAGC 420
TCAGAGTCTG GAATCTGTTC ACGCACAGCT AGGCTGGAAA GCAGTTGTAT CAAGCAGAAG 480
ATGAGGAAGT CAAGAGCTGG CCGAGGATGA TTTTCTGTCC TAGAGAAAAA CATCTATGTG 540
GCACCTTCAT TCTTCCCTAG GGAGCTCTTG TTCTTTGCAG ATCTCCTCCA TCTTTCATCC 600
CTGTTCCCCA AGCCTCAGCC TTTTCGGTGT TCAGTTTCAC CAGCAAAAGA AAGGGAGAAG 660
CAAGATTCAG GTTTCTTCTT CCTTTTCCCC TTAAGCCAGG GTGTTGTTCA AGCTCTCACC 720
CCAGGTGTAA TTTCAGAGCC TTCTCATGCG TGCTGGGTAA TCTGCGAGAG GCCAACAGGT 780
CATTGGGCAT TAAGCCCAGG AAACCTGCCT TAGACCCTGG TGGCAGCAGG CCACCAGGTT 840
CCTCTTGTCA AGTCCAGACT TGCTTGCTTG ATCCCTTGGA AATTTGATTA TAAAGAGCAT 900
TGCCCTGGTA GCTTGTGGTT TGACACTCAG ATTGAAGTTT TGATTTTGTT TTAGCAGAAA 960
AGAGTGGTTT CCAAAACCAA CTTAAACTAG ACTATAAAAT TCTTCCTGGG TCAGAAGTAT 1020
TAGGAAAGAC AGTGTTGGTG TACTGGCTTT ACTCACAACT TGTCTTTTTT TTTTTTTTTG 1080
AGATGGAGCC TCACTCTGTA TCCCAGGCTG GAGTGCAGTG GCATGATCTC AGCTCACTGC 1140
AACCTCTGCC TCCTGGGTTC AAGCGATTCT CCTGCCTCAG CCACCCGAGT AGCTGGGATT 1200
AAGGTGTGCA CCACCATGTC CAGCTAATTT TTGTATTTTT 1240
|
