| Tag | Content |
|---|
EnhancerAtlas ID | HS076-16694 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr13:100800220-100801360 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr13:100800593-100800607 | CTGAGTCATCTCTT | - | 6.67 | | RREB1 | MA0073.1 | chr13:100800660-100800680 | ACCCCACCCACCCCACCCCT | + | 6.93 | | STAT1 | MA0137.3 | chr13:100801286-100801297 | TTTCTGGGAAA | + | 6.02 | | STAT3 | MA0144.2 | chr13:100801286-100801297 | TTTCTGGGAAA | + | 6.32 | | Sox3 | MA0514.1 | chr13:100800980-100800990 | CCTTTGTTTT | + | 6.02 | | Stat4 | MA0518.1 | chr13:100801286-100801300 | TTTCTGGGAAAGGA | + | 6.27 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_33219 | chr13:100799632-100800803 | H1 | | SE_33219 | chr13:100800852-100802283 | H1 |
|
| | 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 |
| GH13I100147 | chr13 | 100800218 | 100801146 |
|
Enhancer Sequence | CAGATGGGGT CACACTGTGT TGCCCAGGTT GGACTCGAAC TCCTGGGCTT GAGTGATCCT 60
CCTGCCTCAG CCTCCTAAGC CGTGGGGACT ACAGGAACTG GGCCACTGCA CACGGCAGTT 120
TTAGTCTTTT TATTTTTTAT TTTTTGAGAC AGGGTCTCAC TCTGTTAGCC AGGATGGAGT 180
GCAGTGGTGG AATCACAGCT CACTGCCACC TTAGCCTCCA CTTGGGAAGC CTCTTGGGTC 240
TGCCACTGCT TGTCAGAAAC TTTTTACTCT GAATTATGTC ATATCTCAGG TGTTTTTACC 300
TAGTTATTTT GCACATTACC CTTCTCAAAG GCATTTGTTC AAGTTTTTCC TAAGCTAATG 360
AAGGAAAACA AACCTGAGTC ATCTCTTGGC TGTCACTCTG CCTCTCCTAC TCTTTACATC 420
CAGCCATATG TACAGTCCTC ACCCCACCCA CCCCACCCCT ACTCTACTTT TTCCTCTGCT 480
TTATTCCGCA GTCCTTTCAT TTGTGGTCTG GTACCCACCA GCTACACTGA CATGACTCTT 540
GCTAAGGTTT TGCTTGAATA CTTGATGTCT CCTTTCTCTC TGTCATTCCT CCCCTTCTCC 600
CTTGATGCTT CTACTAAGGG GTCAGTGGTA TGAGAAGATA GTTCTCCTCC TGCTGGTTTT 660
CATTATTTTG TTGTTTACTG TATCGTCAGG AATGCATGCT TGCAAGACAA AGACTAAAAC 720
AAAAAACAAA AAACCCAAAC AGCAAAAAAA CCCCAAAACA CCTTTGTTTT GGTTCCGAGA 780
TCGATTCAGT ATTAGTTCCC TTTTGTGAAA TGAAAACAGG ATTGTAGAAA ATGGGCTGGG 840
AATTTTGCAA CTGGCAAAAA CGTATTCTCT TTTTTTCCTG TAGTTTAAAA TTTTACCACT 900
TTGAAAATCA TGTAAGTTAT CTTAGAAGAA AAATAGTAGT CCACTAATTC TACCATCCAA 960
AATAACCATG AATAAATATG TCTTGGTGCT ACACATGTAG TTTTTCAAAA TGGAATCAAA 1020
GCGAATCTTT AAAAAAAATC ATTTTGTTTT CTATGATCAA ATTGCCTTTC TGGGAAAGGA 1080
CATGCCAGAA TGTTAGTTTT TTAAAACTTA TAAAAGTATC TTTAGATACT TTGAATGAAA 1140
|
