| Tag | Content |
|---|
EnhancerAtlas ID | HS147-41081 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr8:116439240-116440390 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr8:116439975-116439986 | ATGAGTCATCC | - | 6.62 | | JUN(var.2) | MA0489.1 | chr8:116439975-116439989 | ATGAGTCATCCTTC | - | 6.35 | | JUN(var.2) | MA0489.1 | chr8:116439970-116439984 | AAGAAATGAGTCAT | + | 7.12 | | JUNB | MA0490.1 | chr8:116439975-116439986 | ATGAGTCATCC | - | 6.62 | | Lhx3 | MA0135.1 | chr8:116439521-116439534 | AAATTAATTAAAT | + | 6.07 | | TFAP4 | MA0691.1 | chr8:116439931-116439941 | AACAGCTGAT | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_55889 | chr8:116437383-116449753 | u87 | | SE_67761 | chr8:116437383-116449753 | u87 |
|
| | 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 |
| GH08I115426 | chr8 | 116439135 | 116443622 |
|
Enhancer Sequence | TGTAATCCCA GTGCTTTGGG AGGTCAAGGT GGGAGGATTG CTTGAGGCTA GGAGCTTGAG 60
ATCAACCAAG GCAAACACAG CAAGAACGTG TCTCTACAAA AAGTTAAAAA AAAAATTAGT 120
TGGGTGTGGT GGTATGCATC TATAATCTGA GCTACTCTGG AGGCTGAGGA GAGAGGATGG 180
TTTGAGCCCA GGGGTTCTAG ACTGTAGTGA GCTATAATCA TGTCACTGTA CTCCAGCCTG 240
GGCAACAGAG CGAGACACTG TCTCTAAAAT AGATAAATAG AAAATTAATT AAATAAAAAA 300
GAATTTTTGA ATCAACTATT TAATAGAATA CTCTTGTTTG ACTATCTTTG TCCCTTTTTA 360
AATAATCATC ATTGCACATA TGTTTGCAGG ATAACATATG ATAGGCCTAG TCTCATTATC 420
TGATATCCTC AGAATGATCC TAAGAGGCAA GTATTATTAT CATTATTATT ATTATTCCCT 480
CCACTTTATA GATGAGAAAA CTGAGGCTTA GAAGCAATTT GCAACTGCTG AATAGTAGGG 540
CTAAGATATA AACCCAGGTT GCCCTCACTT CAAAGCCACA GTGAACCATG TTTCAGGCCT 600
TATTACTAAA GAGGAGATTG GGGAATTTTT ACCAAAAATA TTACACCATA TCCTGGCCTT 660
AAAGAACGCT TATCTCTTCA AACCACCCAA TAACAGCTGA TTGAAATTAT GCAAGTTTTG 720
AGGTACCAGA AAGAAATGAG TCATCCTTCA TCAGATATGG CAACGAGCTG TTTTGAGGTC 780
GACAGACACA GTCATAGCCA GAGGAACAGA GCACTTGGCT GATGGAGGGG GCAGTGCTGG 840
GGAGGGGGGA GGGGTGCAGT ACATGTGTTT TGATCCTGCT GTGTCAAAAA AAATAAAAAA 900
AGTATGTGAA ACAGGCCGCT GCTTAAAAGC AGAAGTTGGT GACACCACTG ACTTAGCCTC 960
TCATAGCGCC TGCTACATGG GAGGTTAGCT GTGAATGAAA GTCTCTCTTT GCTTTTGCAG 1020
AAGACTTGGC TAGAGTTGGG GCAAGAAAAA TGGTGCTGGG GTTTTGACAT GCTCTGTAAA 1080
CACACATGTT CAGGTAACAA TTTACTAGAT TTCTTTTATA TATGTGTATG TTCCAAGGCA 1140
GAGACCTTTT 1150
|
