| Tag | Content |
|---|
EnhancerAtlas ID | HS129-00588 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:24626100-24628510 |
Target genes | | Number: 16 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU4F2 | MA0683.1 | chr1:24626917-24626933 | CTCATTAATAATTTAT | - | 6.5 | | TFAP2A | MA0003.3 | chr1:24626588-24626599 | AGCCTCAGGCA | + | 6.32 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_26668 | chr1:24627196-24629306 | Esophagus | | SE_36021 | chr1:24627327-24628968 | HMEC | | SE_64493 | chr1:24627524-24629050 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I024300 | chr1 | 24627197 | 24629306 |
|
Enhancer Sequence | TGGTTATTCA TTTTTTAAAT TGAGACAGGG TCTGGCTCTG TCACCCAGGC TGCAATGCAG 60
CGGCACCATC ACAACTGACT GCAGCTTCAA ACTCCCCAGC TCAAGGGATC CTCCCACCTC 120
AGCCTCCTGA GGAGCTGGGA CCACAGGTGT GAGCCACCAC GCCTGGCTAA TTTTTAAAAA 180
AACTTTTAGT AAGACAAGAC ATCACTGTGT TGCCCAGGCT GGTCTCAAAC TCCTGGGCTC 240
AAGCAATCCT CCTGCCTTAG CCTCCCAAAG TGTTGCAATA ATAAGTGTGA ACCACCACGC 300
CTGGCTTTTT TTTTTTTTTT AAATAATTCA CCATTTTAAA GTGTTACAAC TCAGCGGTTT 360
TTGTATATTC ACAAGGTTAT GCAACTATCA CCACTGTCTA ATTCCAGAAC ATTTTATCAC 420
CCCTCCCCCA CAAATAAAAC CCGTACCTAT ACCTATCAAC CGTCACTCTG AATTCCTCCC 480
TAACCCTTAG CCTCAGGCAA ACACTAGTCC ACTGTCTGTC TCTATGGATC TGCCTATTCT 540
GGGCATGTTA TATAGATGCA GTCACTCAGT ATGTGTCTTT TGTGTTGGTT CTTTTCAGTT 600
AGTATATGTT TTTGAGGTTC AACCATGATG TACTTTACTC CTTTTATCGC TGAATAATAT 660
TCCATTGTAT GAATGTACCA CGTTTTGTTT ATTCATTCAT CAGCTGATGG ACATTTGGAT 720
GTTTCCATTT TTTTTGGCTA CTAGCCCTTG AAAATATAGC ATTCAAATGA CGTGTTGGAA 780
AGGTAAATCA GACTTACAGA AAAAAGAATA AAAATACCTC ATTAATAATT TATTTATATT 840
CAATACATTT TGAAATAAGT TTTTTTGTTG TTGTTGGTTT TTTTTTGTTG TTTGATTTTT 900
TGAGATGGAG TTTCGCTCTT GTTGCCCAGG TTGGAGTGCA ACAGTGCAAT CTCGGCTCAC 960
CACAACCTCC GCCTCCCGGG TTCAAGCGAT TCTCCTGCCT CAGCCTCCCG AGTAGCTGGA 1020
ATTACAGGCA TGTGCCACCA TGCCTGGCTA ATTTTGCATT TTTAGTAGAG ACCGGGTTTC 1080
TCTATGTTGG TCAGGCTGGT CTCGAACTCC CGACCTCAGG TGATCCGCCC ACCTCAGCCT 1140
CCCAAAGTGC TGGGATTACA GGTGTGAGCC ACCGCACCCG GCCCAAAATA ATTTTTTATA 1200
TATGGGGTTC AGTAAAATAT ACCATTGAAA AAAACAAGCC TAGAAACAAA GCAGAGGAGG 1260
TGCGACTGTC GGGGAGGGAG GGCAGGGACC TTCCTCCCCG GGTCTCTTTG TTCAACTCCC 1320
TGCACCCAGT GGTGGACTTG GAATGAGGGG CGAGGGAGGG CCTGGGAGGA GCAGCCACTT 1380
TTGGAGTCGC TGTGCCTTGG CACTTAGGGG AGCTGCAGAA AGCACAGGTC CAGGCAGGAG 1440
TTGGTAGATT TCCCCCTGGG AGGGCACTCA GGGCTGGATT AATTGGACAA AAGGAGTAAC 1500
TGGAGTGGCC AATGACAACA CTGCCTTCTC CTGGCACCTG GCCTGCGCCA GGCTGCGGAG 1560
TTGCTCAAGG CACTTTTTGC TCAAGTACCT GCAAGCTCCT GTGCTCCTCT CCTTTGCGGG 1620
GGAGCAAAGG CAGCAACTTG AGAGGCTACA TTGTCTCTGG GAAGCAGGGA CTGGAGCCCA 1680
GGCCCTGCTC CATCACTGTT TTGTTGTGTC CTTGGGCAAG TTCTTTCTGC TCTCTGGGTC 1740
TTGATTTCCT CGTGGGTCAG ATGAGAGGAC TGGATTAGAT AATCTATAGG GTGTTTTCCA 1800
GCTTTAACAT TTTAGAGTTT TGAAAACAGT CCTGAGTCAG ACAGACGTGG GATCAAAGCC 1860
TAGCTTTATC CTTACCAGCT GTGTAACTTC TCTGTGCCTT GTTTCTCTAT CTTTAAAATG 1920
GAGTAAATAA TAAATAGTGA CTTCACAGGG TTACTGAAAG GTTTAAATAA GGTAACTGTT 1980
GCCAACACTT GGTGCTTACT ATTACCAAAC ACTGTCCTAA CTGCTTTGCA CAGATGAGCT 2040
TATTTAATCC TCCCAGCAAA TCCAAGTTCC TATAGTGAGA ATGTGACAGA GAGGATTTTG 2100
GACCCAAGTA GTCCAGCTCC AGAACCTGTT TCCTCGTCCA CCATGCTGAC CTGCTTTCAG 2160
TACAGGTAGG AGGCTGTGTC CTCAATAAAT GCTAGAGGGA GAGGAAGGCA GAATTCTATG 2220
ATTGTTAAAA TACTTCTGAT GGAAATCCTA GTATGTTCCA CATTAAATAG ATGCGGAAAC 2280
CAAACTCAAC AGGATGAAGT GATGAGCTCT GGACCACCGC CAAAATGGTG ACAGAGCAAA 2340
ACCCAGATAT TCTGGCTCAG AGTTCCCCCA AGTATTTGGA ACCGGAGTGG ATCTCAAGTT 2400
ACACATGCAA 2410
|
