| Tag | Content |
|---|
EnhancerAtlas ID | HS105-31598 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr16:75516530-75517780 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SCRT1 | MA0743.1 | chr16:75516535-75516550 | TTGCACCTGTTGCAT | - | 6.05 | | SCRT2 | MA0744.1 | chr16:75516537-75516550 | GCACCTGTTGCAT | - | 7.12 | | SNAI2 | MA0745.2 | chr16:75516536-75516546 | TGCACCTGTT | - | 6.02 | | ZNF263 | MA0528.1 | chr16:75517604-75517625 | GAAGGAGGAAGGGCAGGGGCT | + | 6.03 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_23275 | chr16:75516865-75517857 | Colon_Crypt_1 | | SE_24337 | chr16:75517075-75517292 | Colon_Crypt_2 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 75516723 | 75517010 | | chr16 | 75517059 | 75517166 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I075482 | chr16 | 75516731 | 75521347 |
|
Enhancer Sequence | TCTGTTTGCA CCTGTTGCAT CTGCAATGAT CTCAAGGCTG GGTGACTTTG GAAGGGAGGA 60
GCCTGGAAGT TTTCTCCTTG CTCCTGCATC CTTTGCTCCT TGCCTGCCCC CTTCCCCTGT 120
CCACATCGCC CACTGAGAGA AGCCAGGGTC TAACTTGTGA GCAGATCTCC TCTCTGCCCA 180
TTTCCCTCAT CAGGAGGCAA CAGGGGTGGG TGGAGGATGC CCAGCAGCTC TGTCACCAGC 240
CGACTCCAGA TCCCACAGCC ACTCTGGGAA AACCTGGAAG ACAGGGAGAG TAGCCACTCA 300
TCTGCTCTGC ACATGATCAA CGCTCCTCCA GTGCCAGTGG GCTGACGATG GTTGGCTTCC 360
TGCCAATGGG GCGCCGAAAG AGAAGGGAAC TCATTTTCTG ACTTCAATGA TCACAAGTGC 420
TAGGTGCTTC AAGTCCACGC GATGACTTAA CTCAACGGGC CCTGAGGTGG GCACGATGAT 480
GTCAATTTTT CAGGTGAAAG ACTCAAGGCT TGGAGAGACA GCGAGAAAGC TGGGACCCCA 540
GGACTCCTGT TCCTAAGCTT CTGGCACTTC TGATCCCAGG CTGTGGGCTT CTCCCACCTG 600
TGATTGCTCC CTGCAGAGTG CAGGACCCTG CTGCTCTGGC CCAAACACAG TTGTCCTGGC 660
CAGCTCAGCC CTTCCCTGGG TAGGGAGGAT CTTGATCCCA AGCCAAGGTA TTTGTTACCT 720
GTGTTCCAGG GAAGCCAGAG GTCTTCTTAA GTGACTCACA CACTACAGGA ACTGCTATGA 780
GATCCTATTA CTGAAACTCA AGAACTAGGA AGGTGGTTGA ATCATCCTAC GCCACAGAGT 840
CTCCAGAAGA CCAGTTCCTA GCTGAGAGCA TTCTGATAGG AGCCTTACGT TCAGCACAGT 900
AGACATTTGG GCCAAGGTTT TGACATTAGG AAGAACAAGT CAGGCAGGCC CTGTGATAGG 960
TACTTCTGTC TTCATGATTA AATGCTATCA TCCCAAGTCC CTGGGAGGCA GAAATGACCA 1020
TACCTCTCTG TTTTAATTGA AGCAGTGGGG CTCAGAGACA TGAATATCCA GTAAGAAGGA 1080
GGAAGGGCAG GGGCTTAAAT CCAAGAGCCA GCCGGGTACG GTAACTCATG CCTGTAATTA 1140
GGGCACTTTG GGAGGCTGAG GCGGGTGAAT TGCTTGGGCC CAGAAGCTCA AGACCAGCCT 1200
GGGCAACATG GCCAAACCCC ATCTCTACTA AAAATACAAA AATTAGCCCA 1250
|
