| Tag | Content |
|---|
EnhancerAtlas ID | HS145-06400 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr13:20694560-20695920 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYA | MA0060.3 | chr13:20694854-20694865 | GACCAATCAGA | + | 6.14 | | NFYA | MA0060.3 | chr13:20694905-20694916 | TCTGATTGGCT | - | 6.32 | | NFYB | MA0502.1 | chr13:20694849-20694864 | GAAGCGACCAATCAG | + | 6.36 | | TBX20 | MA0689.1 | chr13:20695319-20695330 | TAGGTGTGAAA | + | 6.14 | | TBX2 | MA0688.1 | chr13:20695319-20695330 | TAGGTGTGAAA | + | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr13 | 20695387 | 20695695 | | chr13 | 20694627 | 20695029 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I020118 | chr13 | 20692140 | 20695980 |
|
Enhancer Sequence | ACAAAAGGAG AGATTTATCG AAAATGAAAG TACGCTCCAC AGGGTGGGAG CCGCTGGAGC 60
ATAGGGGCTC TTTTTACAGA ATTTTCTGGG GTTTAAATAC CTTCTAGAGG TTTCCCATTG 120
GTTACCTGGT GTACACTCTA TGTAAATGAA GTAGTGACCT GCAACCAGAG GCTGAGGTGA 180
AGTTACAAAG GTTACACCCG ATGCAAGCCT CTGTTTGCAA AGTGAAGTTA CAAAGTTACA 240
GTTCTATGCA AAGGAAGACT TGGCCCACAA TCAAGCTGAT TGGTTGTGGG AAGCGACCAA 300
TCAGAGGCTG AAGTGAAGTT ACAAAGTTAC AATCCTATGT AAACGTCTGA TTGGCTGCCC 360
TCAGAGACAC TTTCAATTTT CCATCTGCCA GGCAGAAAAG GGTGGGGGTT TGCAAAGGGA 420
GTAGCCTCCG GTTTTTTGTT TGTTTTTTCT TTTTTGAGAC GGAGTTTCAC TCTTGTCGCT 480
CAGGCTACAG TGCAACGGCG CGATCTCCGC TCACTGCAAC CTACGCCGCC CGGGTTCAAG 540
CGATTCTCCT GCCTCAGTCT CCCGAGTAGC TGGGGTTACA GGCGCCCGCC AACACGCCAG 600
ACTAATTTTT GTATTTTTAG TGGAGACGGG GTTTCACCAC GTTGGCCAGG CTGGGCTGAA 660
ACTCCTGACC TCAGGTGATC CGCCCACCTC GACCTCCCAA AGTGCTGGGA TTACAGGCGT 720
GAGCCACCAT GCCCGGCTAC CTCCGGTTTT TTTGTTACTT AGGTGTGAAA AGTTGGGGTT 780
TTCCTTTTGA TTTAGTTCTA GGAAGTCAGC GTGAAATCGG CCTTAGGTTC CCTGCCTCCA 840
GACCCTATTC TCCGCCTCAG AAAGTCACCC AATGATAACC AATGCACTTT TCTCACCACA 900
CGATTTCCTC ATTCCTGCTT GAGCTGCCTT ACCAAAGCCG ATTGTTCTGC AACACCCAGC 960
CGAGTGCCTT CTGTTTTGTA GTCTGGAGGC TGCCTGTTTC ATACATTGCT AATAAGAGTC 1020
AATTAAATCT TTAAAACTCA ATTTGTCAAA ATGTTGTTCT TTGGTGTCAG AGACCAATAC 1080
TGTAGGGAAT TTGTGTTCAT TGACTGAGCT CAAGTACATA GAACAGCTGG AGGGAAGAGA 1140
CGCGCAGGGC AAGGTATGAG GTGGGGGCTG CAGGTGCACC ACATTCCCAC AACTTGGAAA 1200
CTCTTCCAAC CTGCTTGTTC AAGAGCTTTT TTAGAGCTTG ATTTCTAGTC CCCTCCCCTT 1260
CTCACAGGTC TAGGGGTGAG GCTGAAGGAT CCAACCTCCT ACTTACCTGG TCTTTCCGGT 1320
GACCAACCCC ATCCTGAAGC TATCTAAGGG TTCACCCTAA 1360
|
