| Tag | Content |
|---|
EnhancerAtlas ID | HS145-21344 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr5:136957820-136958930 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| USF1 | MA0093.2 | chr5:136958626-136958637 | GCCACGTGACC | + | 6.62 | | USF2 | MA0526.2 | chr5:136958624-136958640 | GTGCCACGTGACCCAG | - | 6.61 |
|
| | 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 |
| GH05I137620 | chr5 | 136956583 | 136959255 |
|
Enhancer Sequence | AAGAAAGGGG GAGAAAGTTA TCATCTTAGC TTCTCCAAAA TTACTCAGAG TCCCAGTGAG 60
TTCATGAATC CAAGATATCC TGAGTCACAG CCAAGGGAAA TGTGTGCAAT TTTTATCCTA 120
ATATTGAAGT GGACTCAGGC TGCTAGCAGC TGGCTGTTCC CCACTCCAAC AGCCAAGTCC 180
TGGCAAGACA CTTGAACCTA CGAGCACAGT CCCTCAAACA CCACTGACTA GTGGCCTCAC 240
CCTGTGTCAT CACATGGACT CACTGTGGTG ACTCCCATCC CCAGCCCTAG CACCCAGCCC 300
AACAATGCTC AGCGCCCAGG GGCAGCTATG CAGTTCTAAA TTTGAATCAC TGTAAGAGAA 360
GCAATGGGTG ATTCATCTCT ACTTTTAGAA GACACTGGAA TGAAGCGGAA AGTACAGCAG 420
GCTGCCTTCA TGGGAGCAAG AAAGACTGAA TTCCATTCCT AGCTCTGCCA CCAGTCAACC 480
TGCACTATGG CCTTTGGCAA GTTCTTTGAC CTCTTTAGGC TCAGTTCCCA CACAAATGTC 540
ATCTAAGAGA CCCTGCCAGT GTGACAATCT CGACTTTGAT AAATGCTCCA GACATGTATG 600
CTATGTTACT GTTTTAGTCC GAGTGAACCA TGCTCAGCAC CTAACTATAA ATCCACGCAT 660
GACCCAAAAT CTCACTGTAA GGGACTGAGG CTACATGGCA GATATTACAG GTTGATTCCG 720
TCAACATCCT TCCTACTTGC TATCCTCGAC TACAGCCACC AGCAAGTTGC AAGCTCAGGT 780
TCCCAGACTG CCTGGCAGCT AGATGTGCCA CGTGACCCAG TGCTGGCCAC TAAGACTGTA 840
AAGGCAAGTG TGCCAGTGTT GCAACGCTGG CTTTGTTCTT GTTGTGACTG GAATGCTCAC 900
GCAAGGCCAA GGGGAGGCAG CAGCCCTTGA TAAAGCTGGC AGAATAGAAA AGAGAAGAGA 960
AACCTGGTTC TGTCAGTCTG AGCCCCCAGG CCAACCTTGG ATTTCTTTCT ACTTGAGACA 1020
AATACACTCA CTTCCTTATT TAGGAAAGTA TCTGTCAGGG TTTCTGGTGC CTGTTGCTAA 1080
ATGAAATCCT AACTTACAGG TGTTTACAGG 1110
|
