| Tag | Content |
|---|
EnhancerAtlas ID | HS053-11745 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr13:111242480-111244000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ALX3 | MA0634.1 | chr13:111243693-111243703 | TCTAATTAAA | + | 6.02 | | E2F6 | MA0471.1 | chr13:111243096-111243107 | CCTTCCCGCCC | - | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_31501 | chr13:111242853-111243720 | Gastric |
|
| | 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 |
| GH13I110590 | chr13 | 111242574 | 111243362 |
|
Enhancer Sequence | ACTGCTCAGC AGAGAAGGGA ATCAAACTGT TGACACAGGC AGCAACCCGG ATGAACCTCC 60
AGAGAATCAC ACTGAGCTGG AGGGAAAATA AAGCAATTCC AAAGGTTACA TACTGTAGAT 120
TCCATTTCTA TAACATTCTG GAAATGACAA AATTATAGCA ATGGAAAACA GTTCCATGGT 180
TGCCAGGGGT TAAGGAGAGG GTTGGGGTGA AAGGGAAGTG AGTATGGCTA CAGAAGGTCA 240
ATATCAAGGA TCCTTGTGCT GACAGAAAGT TTGTAAATTT GGCCTGTAAC AATGTCACCA 300
TTCTGGTTGC CATCTTGTAC TGTAGTTTTG CAAGATGCTA TCATTGGAGG AAACTAGGTG 360
AAGAGCATTT GAGCTGTTTC TGTATTATTT CTTTTAACTG CATGTGATTC TATAATTATC 420
TCCAGTAGTT TTAGAAAAAA GTCGTGGTGA GAGGCAAAGA GAATGATGTA TGTAAATTCC 480
TCAGCACAAT GCCTGGCAGG TAGGAGGGAC TTTAGTGCTA TCACTGAAAA GTCCTGGGCA 540
AGCCAGGACA GCTGGTCACC CACAGGGCAG GTCCAGAATT CGCTCACTCA GTGTCGCCAA 600
GGACTCAGGT TTTCCACCTT CCCGCCCTGC CCTCCTTGGA ATGCTGGCTC ATGTTCAAGT 660
CGGATGCCCT CAGGGTTACG GGGCAGCTTT TCCAGTTCCA GGCTTCATGT GCACACTGGT 720
CCCCATGTCT CTCACCTCTC TCTAAGAGCA AAGAAACCAC TCCTGGAGGC TTCCCTCCCT 780
CACAGCTTGG TGGCTATGGT TGCTACAGTG ATGATAAAAA GCCACTCGTT CATCACAATC 840
AGCAAGGGAA ATGGGACCGC AGTGCTGAGG TTGGGCCCGT CTGGATTTAC CTCCAGACCC 900
GGAGGAGAAC CAGCCTTCCT GCGTCAAGTG GCAGAATTCT ATCTATGCCA GCCAGTATGA 960
AGGTTTTGGG TGGCCCCCCA GAGCTGTTCT TCCTCCTTTC TCAGGACTCC AATGGCCTAA 1020
CATGCGTGGC TCTGGGCACC TGAGTTGTGT TTCCTGGACC CGCCAGATCT AAGCGGGTCA 1080
ACACCAGAAA CTGCGCGTGT TCATGTGGTT ATCCTCCAGC ATCTTGCAGG TGCCCCGTGC 1140
ATGTAAAGCA TAGTCACATA TTTGCTTAAA TGAATTCAGT AGCCTTCAAC CTATTGATTC 1200
TGCCTCTCAA ATGTCTAATT AAATCTATAC CCACAACCAT ATCACGATGG TCCACATTAG 1260
AAACTTCATC AGGCGCCAAG CTGGCTACCT AGAGTGTCTC TTAATTTCCG CAGATGCAGA 1320
GCTGCAAATG TTTCTTGCTC TTCTGAGCAC TCCTACATTT GATTTATTCA TTTGGCATTT 1380
TGAAGTGAAG GCAAGACAGT GTTATTGTTA ACTCCGTGCT TTTCTTTAAA ATGTTTCTTT 1440
GCTGGCTGGG GGTGGCGGTT CATGCCTGTC ATCACAGCAC TTTGGAAGGC TGAGGAAGGA 1500
TTACCTGAGG CCAGGCGTTC 1520
|
