| Tag | Content |
|---|
EnhancerAtlas ID | HS145-12946 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr2:99485720-99486830 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr2:99486233-99486254 | CCCCAGTTTCAGTTTTCTTTT | + | 6.93 | | KLF4 | MA0039.3 | chr2:99486427-99486438 | CCACACCCTCC | + | 6.32 | | Klf1 | MA0493.1 | chr2:99486425-99486436 | GGCCACACCCT | + | 6.32 | | Mafb | MA0117.2 | chr2:99486630-99486642 | AGTCAGCAGTTT | - | 6.22 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_08130 | chr2:99483646-99486056 | Brain_Inferior_Temporal_Lobe | | SE_24439 | chr2:99484486-99486777 | Colon_Crypt_2 | | SE_27533 | chr2:99484074-99487516 | Esophagus |
|
| | 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 |
| GH02I098867 | chr2 | 99484176 | 99487382 |
|
Enhancer Sequence | CTCTCACAGA AGTACCCGTG CGCCAGGAGG AAGTGGGGCT TCTGCCAAGC CCAGCCCTCC 60
TGTGCCCCGT GAGCTCCTTG GGCGGGTGCA CAGGCACACA GCAGAAAAGG CCGTCTAAGA 120
AACGCAATGC ACTTCCGCCT TCCACTCCAA GCCCTGAAGG CCGGGATGGG GGTGGCCTGG 180
CTCTGTAGGG AGTTGGACTC GCCTCCCTGT GATTGGCATC CCCACTGAGT TGCTTGGGCT 240
TTGTTGACTG TGCTCACCAT GGAAGCAGGC AAAGGGCAAT GGCAGGTGAG GCTGCATTCC 300
CCATCTGAGG AAGGGCAGGG CCCAGGAAGA AAGAGGAATG CTGAGAAAAT CGGAAACAGC 360
TTCTGAGCCA GACACACCCA GGCCCAGGGC TCTCCTCTCT CATTCCAGCA CCAAAACCAC 420
CCGGCCCCTC CTGCCTCGCC TTGATGTCCA CTTGCTATCT CAGTGCGAGG GACCCTGTGG 480
GAGGCACGCT CGTCTCTGCG CTGCACACTT GCTCCCCAGT TTCAGTTTTC TTTTTACTTT 540
TCCTTAAAGG CCCATCGTGT TACCTCAGGT CCTTGATATG CTTTGTTAAC TGCTTTCCTG 600
GGGCCTTCCC AATGCTCCTT TACCAGGGAC CTGCTTGCCC CACTCATTGT TGCACTGATG 660
GGATTTCCAG CCCTCCCCCT GGAGCCCAAA CCTGACAGGT GCAGGGGCCA CACCCTCCCA 720
AAAATCACCC ACTGAGCCTG CCCAGCCGGC TCCCCAGCCA CCCCACGTGA CACAGCCACT 780
TGCCCTGGTG GCTCCTATCT GATTACCTGC AGCTGCCACT TCAAAATAAT AGACTCCTGC 840
AACTGGCATC ACAATGCCAC CTGACTCAAG TTCCTCCCAA GTCTGATGGC TTGCCAACTG 900
CAACCGGTAC AGTCAGCAGT TTCCAGGCAA TATCTGGAGT GTTGACAGAG GGCTCTGGGT 960
GGCAGGTGCG ATTCTATGTT AGTAAAACTC AGGAACAGGC AGCAGCAAGG GCAACTTCTG 1020
AAGATGGTTC TGAAAAAGCC CTAGTTTGCT TTTCTGTTTT CCAAATGGCA ACTGTATATA 1080
GAATTCTACT CAAATGGCCT ACAATTTAAT 1110
|
