| Tag | Content |
|---|
EnhancerAtlas ID | HS106-00383 |
Organism | Homo sapiens |
Tissue/cell | iPSC |
Coordinate | chr11:20048250-20049490 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Atoh1 | MA0461.2 | chr11:20048427-20048437 | AACATATGTT | + | 6.02 | | Atoh1 | MA0461.2 | chr11:20048427-20048437 | AACATATGTT | - | 6.02 | | NFIL3 | MA0025.1 | chr11:20048432-20048443 | ATGTTACATAA | - | 6.32 | | Rhox11 | MA0629.1 | chr11:20049285-20049302 | TTTTTTTACAGCATCGT | - | 6.46 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_36574 | chr11:20048219-20050281 | HMEC | | SE_65102 | chr11:20048155-20050309 | NHEK |
|
| | 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 |
| GH11I020026 | chr11 | 20048227 | 20051270 |
|
Enhancer Sequence | ATTAAAATGT GTAAAATGAA TAGATAAATG CGATGGTTGA ACACTCATGT GTCTGTGTTT 60
AAATCTCAGC CTCAACATTT CTTAGTTGTA TGACCCGTGG GACTATTTCT CCAATCCTCA 120
ATTGCCTCAT CTGTAAAATG GGTATAGTGT TAATATTTAT CTAACAGTAA CTGGGAGAAC 180
ATATGTTACA TAACAACAGA GCCTGACACA TAGCAAACCA TTAATAAGTG TTGGTGATTA 240
TTTTTATCAG AGTTTGGAGG ATTAACTGAA ATAATGTATG TAGTGCAGTT AGCACAGGGG 300
CTGACAACTG TAAATGTCGA TTAAAGTTGG CTATTATTAT GCTTTCCACA TAGACTACAA 360
AAGGTAGGAC TCTGCAGGAG CCCTGCTTCA TTCTTTGAAG GTGGATTTTC TTAACAGGCC 420
CCAGCAATAG TTAGAGGAGA TGATGCTCCC GAGAAAACCT CCTGGGGAGG AAATAGTTAA 480
CATACCTGTT TGGTGGGAAA TGTAGGTAGC CAAACCCTTT CTCTTCCCCA GGGGTTACTA 540
CTAAGCCTAC AGTTAGGCTT GCTCACTCAT CCACACCAAA GGATCTCGTT CCGCTCGGGC 600
CCCGGGGTTT CACGGGAACA ATTGCCTTGA ACAATAGCCA GAAAACGAGT TCCACCAGTC 660
TGGACTTTTT TGCAACTGAA TGCAGCTGTC TGGCGGGGGG CATGGGCCAG CCCTGTAAAT 720
GGGCTGTGCC TTGATTCTGG AGCAGAACTG GAAAATTGAG CAGGTAAGTC CTGGATGCAG 780
CTGGTCACAG CTGCGCAGTG TGAGCTTAGT CACCTGGAAA GAGGCAGACA GAGGGGCGGG 840
GGCTGGCCCA GACTGTTTCC AAGGACAGTA AGGGCCTCCT GGAAGCAGAC CCAGCCTTTG 900
GAGTTTGGGG AGGATTAGGA TCCTTGCTTT GTGAAGACTG CTTTTCAGAA CCGTAGTTAG 960
AGAACCTCAT CTCTGCTCAC CGGCTGTGGT TTTATTAGTA AGTAGAGAGG AACTAATATA 1020
TATCTACAAT CTGATTTTTT TTACAGCATC GTTTAGCATG TCTTTCCCTT GAATAAACAA 1080
CATTATCTCA CAGGGAGTTC ATTTGAAAGG TGTAATGATC CTCCCTCCAG ATCCTTCAAT 1140
AACTCCTCCT CCCGGAGTCT TTTGCTGAAA GCAAGGGTGT GTATATCCTA GTGGAAAAAT 1200
CTGTTTAATC ATCCCTGGAA CCTTGGGATT CTATTTTGCT 1240
|
