Tag | Content |
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EnhancerAtlas ID | HS129-19185 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr2:26290960-26291880 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr2:26291298-26291308 | TCTAATTAAA | + | 6.02 | JUN(var.2) | MA0489.1 | chr2:26291638-26291652 | CTGAGTCATTTCCT | - | 6.73 | NFE2L1 | MA0089.2 | chr2:26291634-26291649 | CTTGCTGAGTCATTT | - | 6.88 | Nfe2l2 | MA0150.2 | chr2:26291636-26291651 | TGCTGAGTCATTTCC | - | 6.41 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_09566 | chr2:26289818-26294619 | CD14 |
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| 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 |
GH02I026066 | chr2 | 26289807 | 26293562 |
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Enhancer Sequence | GAAATGACAT TTATACTGCT ACATGAGATA TGATTAGAAG TTAGGTAGAA GAACATCATT 60 CCAGGCAGAG GAAGTGGGCA CAAAAAGGTC CTTAGTAAAG GAGCTTTTTG AGTTCAAAGA 120 ACTGAAAGAT GATGTGTGTT GCAAATGTGA CTTGTGAGGC TAGCAGAAGC AATAGATGTT 180 GAAGACGTGG GTTTGAGCCA GATTGTGCAG AGCCTGGTAG TCCATGCTAA GGATTCGAAT 240 TCCATGGAAG GTTTGAGCAG GGATGTGACA TGGTTAGATT CAATTTTTAA AAGATGGTTG 300 GCCCAGAAAA TGTGGAAAAT GGATTGGAGT TGGAATTTTC TAATTAAAGA CTTATCAAAG 360 ATGTGTTTAA ACTCTTACTG TATACTATTT AATCTTTAAG GATTATGAGC GATTATATGT 420 GAAAATACCT GTCAGTGACT GTGACAGTGA GCCTTTAATT TTTTTTTTGA GGTGATCTTT 480 TTAGTGCCAA ATACATCAGA CAATCCTGAG CCAAGAGACA GAGTTCTGAT CATAGTTAAT 540 TTGGTTTGTG AGCTTGAGCA AGTCATTTAA ACTCTGAGCC TCTTTCTTTA TCTGTAAATT 600 GGGCGTGTTT GAGAAATGTG TGCTTAACTT TAATTGTGTT AATCGCTTAA CTCTGGTTAA 660 CATATGGGCT GAGTCTTGCT GAGTCATTTC CTCAGACGTT GTGGGCAAGG CTTAAAACCA 720 GCTAAGCAAA TTTAGTGATG ACACATTTTA CCTCTTCTGT AGAAGTCAGA TGAAAGAGCT 780 GTTTCAAAAA TGTTTCACTT ATTGTTTTCA TGCAGATTAT CTCTTCGTGG GGGAGAGAAT 840 ACAGTACACA TAGCTCAGGA ACTACTGATG CACTGCCTTC CATTTTAGTG GCAGTTTGAA 900 TTTAAGAATT TCTAGTTTGT 920
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