| Tag | Content |
|---|
EnhancerAtlas ID | HS048-01926 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:95267030-95268420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:95267481-95267502 | CTTTAGTTTCACTTTGTATCT | + | 6.3 | | NKX2-3 | MA0672.1 | chr1:95267687-95267697 | ACCACTTGAA | + | 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 |
| GH01I094801 | chr1 | 95266548 | 95270865 |
|
Enhancer Sequence | TTATTTATTC ATTATTATTT ATGTAGTCCT TCTGTCTATA ACATGTAGTT AATTCTTGCA 60
CAGTGTATGT AATATGCAGT ATCTTTAGGC CACTGAGTGT ACTCCACAGA AGTCATCCTT 120
CTGTCACTGT AACCCTATCA CGTGCACTGA TAACACAAGT ACTCCCAAAA TGACCCAGTC 180
TCCTTTTGAA TTTGATAAAT TGCCTGAATA TACACTTAGG TAAATTTTAA CAATACTTTG 240
CCAAGCCTTC TACCCCACGA AATAATCCTA GTGGATTTAG TTTGAAATAG CATTAAATGT 300
ACAAATTAAC TTTGAAACAA GTCCTATCTT CACAATGTTT TCCTTTCTTG ACATGATGGG 360
CCTTCTGTTT ATTCCAGCCT TCTTTCGCAT TGCTCATTGA AATTTGTGCC TTTATTTCTA 420
TCTGTTACAT TTGTTTCCCA TTCTGCCCCC ACTTTAGTTT CACTTTGTAT CTTCCCATTT 480
CCTTAGAGAA TGAACAGCCA CACATAATGC AATAGGACTT TTATTTAGGG TAGATGAGAA 540
ATCCTAGATC AGTTTTCATT TTACTAAACA ATTAGTTAAC AGAAGCATTG CCTAAGAGGC 600
CTGTGCTCTA ACTAGAACGG CAGAGTTCTC CAAGTCATTT GTTTCATCTG GTTAATAACC 660
ACTTGAAAGC CCTGTGCTCT CTTTCAAGTT ACTTGGCTCC ATCTTCTGGT TTGAATTATG 720
AGTACTTGGA GTAAGGGCAG TTAAAAGTTG CCAGAGCAGG GCTGAGACTG GGGTGAGGTG 780
AGTTGCGCAT CTAGGGTCCA GATTTAAGGA AGCGTCTGCT CTCAGGCCCC CTGGTGCCTC 840
GTCCACCACA CCTGGTCCCA GCCTGCCCCA GGGAACCGGC TGCTGTGAGC CAGCTACCAT 900
CTGGCAAGCA GTTGGGAGAG GGAGCCACCG TTTCCCCCAT AGCTCTGCCC TGGGCCTGCA 960
CAGTGGGAGT TGCTGTCACC GTCCACAAGG AGCACTTGGC CCAGCCTGGC TAATGGGCCC 1020
CACTCTTGTT TCTCCAGGTC ACTTTTGTGT TTTGTAGATG CAAGAGCCAT CTACAGCTGG 1080
AACCGACTGA CAGCCCAACA CCATCTAAAT GCTCTTACAA GATCCGTAAA GCCAAATCAT 1140
TTCCATTTGA GAAGCACTTT GTCTGAACTG TGTTATTGGT CCATGGGTCA TGACCTCCCT 1200
CTAGCCTGTG CCACCCTAAC TGCCCTTAAC TGTCCAGAAC AACAACCACC CCTGCCCCTG 1260
AAGCCTTCCC TGAAAGGCTT CAAGCACAAG AGCTCGTTTT TTAAAAATCC AAGAAGAGCT 1320
GAATATGAGC AGATGAAAGC AGCTATAATA AAATGATTAT AAAACCTGTA TGGGAGGGGG 1380
GTTTAGATAG 1390
|
