| Tag | Content |
|---|
EnhancerAtlas ID | HS040-02393 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:152852010-152853630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:152853495-152853516 | GTTCAGAAAGTGAAAGTGAAG | - | 6.88 | | PRDM1 | MA0508.2 | chr1:152853504-152853514 | GTGAAAGTGA | - | 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 |
| GH01I152879 | chr1 | 152852185 | 152853813 |
|
Enhancer Sequence | AAGAAGAAAC TCTTGCAGGA GGCAGAGGGG TCCAGGAGGC AGGTTTGTTG GACAGGAGCC 60
AGGGTTCTGA AAGTGGAGGA TATAGATACT ATTCACCAGG CAGAAGGAAG ACAGTGGAGA 120
CAGCACTGGC TCAGAGGGGC AGGACCTGCA TCCATGGGGG TGAGGTTGCA GAAGGACTTG 180
ATGTTGCCCT CCCTATGCTA CAGTCAACAA GACTGGTTTC CAACCTGCTG TCCTTCTCTG 240
ATATTGCACA ACCTCCACAT TCAGGACCTA TTCCCAGGAT CTCACTATGG GGGACATGCT 300
TGGAGTGGGG ACATTGGTGG GACTGGTGAG GCAAGCCCCT GGACCTGGGC TCCAGGTGCC 360
TCTGATGCCT CTGCACCTCT GATCACTGGA ATGAGAATTG CTTCTGTAGA AACAGCTCAG 420
TCTGGACTTG TAAAGATGGA CACTAACAAA CTGGACTTCC AAGTGGTGAT GAGACTCTGC 480
ACTTTGGTCA ATTCAGGGCA CTGACCTTCA GAGTAGAGAA AGGTAAACCA GAGACAAAAG 540
ACAGAAAGGT AGAGACAGAA TGAAGACCAG AGAATGATAG AGAGGCAGAG AGGAAAAAAA 600
AATAGCAAAA GGCAAAAATA AACACAGAGA GGAACAACAG AAAATAAAAA CAGAAGGGGC 660
TCACTCCTCC CTCGTCCCTC TCAAAACCTA GTCTTAGGTC TGACCTCTAA GGGAGCAGAT 720
TCAAACAACA AGGAGATACG GACAGATACT GGGCTCCCTG CATACCCCGG CACACCCAAA 780
TTCACCACTG TACAGCTGCA GGGGCACCCA AGTGTGTGCT TGTGTGTGCG TGTGGACACA 840
CACACACACT TCCTGTCAAA CAGCTTTGAA CACTGCAAAG GTGGTAGAGA ACATGGCCCT 900
GTACTCTCTC ACCTCTTCCC TATTTTTATA CTGGTCTGTC TCCGTCTTAT TTCCATTTTT 960
GGTGTGCCTC TCCATTGCTC ACCTCTCTCC TTCCTGTTCT CTCTCGGGCA AGTCAAGGCA 1020
TCGCAGGGCC TGTATCTGCC ACCTCAGCCT CTTTGCAGCT TCCTCTGACC TAGAAGGAGC 1080
AATAGGGTGA CTTGTCCCCA CCCCCATCCT TTAGGAGTCT TTGCTCTAGT GTCTTCCTCT 1140
TAAATGGAAG CAGGGGCCTT TTCCTGAAAG ATAGGATGAA TCCAGGAATA ACTGGCAGAG 1200
ATAGAGTCAT GACTGAATTA AAGCCAACAT CCTAACCCAA GTCACTCTCC CCTTTTTAGG 1260
TGGGAACTGC CCTTGACCCA GTTCAGGCTG CAGCCATATA GCCAGGGACT TAGGATCATG 1320
AAAGGTTTAT ACCAGGTGGC AGGGCCTTAA GAGATAACTC TTCCCTCCCA ATCTTCTCTC 1380
ACCCTAATGC TGTAGTTCAG GAGATTCAAA CATAGGGGTC CTTATAAGAG GTAGCACTGT 1440
GCTCCCCTCC TTCCCACAGA GAAACCCTGA GATGAGGCTC CAATGGTTCA GAAAGTGAAA 1500
GTGAAGAGAG TCTGCGCTGG GGCTGGGTCC AACGTGTGAG TCTGAAAGTT ACTGTTTCTA 1560
GTGGGTGGCG CTGTCGGCCA CACCTGGCTC AATGGGACCC AGTTTGTACA CTATGAACTG 1620
|
