| Tag | Content |
|---|
EnhancerAtlas ID | HS053-00645 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:23801100-23802440 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYA | MA0060.3 | chr1:23801658-23801669 | AACCAATCAGA | + | 6.62 | | NFYB | MA0502.1 | chr1:23801653-23801668 | AGCTCAACCAATCAG | + | 6.31 | | NKX2-5 | MA0063.2 | chr1:23801306-23801316 | CTCAAGTGGT | - | 6.02 | | RELA | MA0107.1 | chr1:23801437-23801447 | GGGAATTTCC | + | 6.02 | | STAT3 | MA0144.2 | chr1:23801871-23801882 | CTTCCCAGAAA | - | 6.02 |
|
| | 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 |
| GH01I023471 | chr1 | 23798426 | 23803276 |
|
Enhancer Sequence | TAGTCTTGCC CTTTCACCCA GGCTGGAGTG CAGTGGCGCA ATCTCGGCTC ACTGCAACCT 60
CCACCTCCCG GGTTCAAGCG ATTCTCCTGC CTCAGCCTCC GAATAGCTGG GACTACAGGT 120
GCGTGCCACC ACGCCCGGCT AATTTTTTGC ATTTTTAGTG AGACGGGGTT TCGCCATGTT 180
GGCCAGGCTG GTCTCAAACT CCTGACCTCA AGTGGTCCCC CTGCCTCAGC CTCCCAAAGT 240
GCTGGGATTA CGGGTGTGGG CCACCGCGCC CAGCCCCCAC AGCTTTAAGT ACCAGTTCAA 300
GCAATGGATG CAAATGTGGT TCAGGCAGCA CCTGCATGGG AATTTCCAGG GTGCTGGTTT 360
AAATGCAGAT TCCCAGACAA TCCCACAAGC TGGCAAACTT GCTGTCAAGT ACATCTGTCA 420
TTGTGTGCCA GTCTGGCATC TGACCTCCTT CCTATGTCTG GGGACTTCCT CACTGCACAG 480
GTCTTGGCAG AGTTCACCTC CTGTGAAAGC TGAAAACAAC AAATTCTTGC TTTTCCAGCC 540
TCCCTTACAC CTAAGCTCAA CCAATCAGAA GCCCTCACTA CAGACTTTGA ATCAGGAGCA 600
CAGTGGAAGA TCCATTCCAA TGCTGGTGGC AACCACAGCA ATGGTGTCTA GTGTTCAGGG 660
AACAGTGACA CAGCGATGGC ATTTAGTGTG TGGCAGCAGT GTCCTGCCAA ACTGGCTCGG 720
TGGCATGATT TTGGCTGAGA TCCTGCCTGC TGCCCAGCCC CAGTTTTCCA ACTTCCCAGA 780
AATTCTGTGA ACTACTGAAC ATTCCCTTTC AGTGCAGCCC TTTTCTGCTT AAATCAGCTC 840
AGGATGGTTT CTCTTGCTTG CCATAAAAAG CCTAAGATAC CACCACTGAA TCATACTCTC 900
TGGGAATGAC GCCAAGTGAT TCTGACACAG ATGCAGGTTT GAAACCCACG GTCTCGATGC 960
TAACAGCTCT CAAATGTGTA TCTCCAGCCC GCTCCTTTGA ATTCCAAACT CACATACTGC 1020
CTTCTTGACA TCTCCACTTG GATGTCTCAA GACCTATAAA GATATACAGA TAGAATTCTT 1080
GGCCAGGCAC AAGTGGCTCA TGCTTGTAAC CCTAACATTT TGGGAGGCCA AGGCAAGAGG 1140
ATCACTTAAG CCCAAGAGTT TGAAACCAGC CTAGGCAACA CAGCGAGACC TCATCTTTAC 1200
CAAGAGAAGA AACAAATTAG CATGGATGTG GTGGCATGTG CCTGTGGAAG CACGAGGATT 1260
GCTTAAGCCC AGGAATTCAA GGCTGTGGTG AGCTATGACT GCACCACTGC ATTCCAGCCT 1320
GGGCAAAAGA AGGAGACCCT 1340
|
