| Tag | Content |
|---|
EnhancerAtlas ID | HS101-12086 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr13:31292780-31294030 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DUX4 | MA0468.1 | chr13:31293926-31293937 | TAATTCAATCA | + | 6.14 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_37797 | chr13:31292228-31294599 | HSMMtube | | SE_59818 | chr13:31293174-31321295 | Ly4 | | SE_63988 | chr13:31292247-31295301 | HSMM |
|
| | 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 |
| GH13I030718 | chr13 | 31292497 | 31295337 |
|
Enhancer Sequence | AAAAAAGGCC TTTTATTCTC TTCATTCCAC AAAGCTCAGT GTCAAAACAT GGGGTTTACA 60
CTGGAAGCTG AGGTCACATC AGTAGCCGGG ATCAGGGTCG CCCTAGCTGC CCAATGCAGC 120
TCCCAGGCCT CCTGTAAAAC CTTGACCTTT GAGGTCATGA CAGCCCTCTC CTGCTATGCT 180
CATAGCTGAC CACTGAACTC CTGGACACTC CCTCCCCCAA GTTCACAGAG AATGTGGGCA 240
CATGCCTTAC AGTCTTCCCT TGATCCAAAC TACTGCCTTC ATCTTGAGTG ACAGCAGCAT 300
CTTTTGGATG TCTTGGCCTG TCTAGCTTTA TTTTTTTGTG TTCTGCCATC AAGTTGCTAC 360
TTCTGTTGCC ATCGTGCCTG TCAGCGCAGT GCAGGCTGTG GTGAAATCCC ACGAACTCAG 420
GCATCACACT GACCGGGTCT GAGTCCTGTC TCAGTTGTCA GCTAGTTGTG CAATGAAGGG 480
AAAGGGACCT ACACTTTCCA AGCCTCAATT CACTCATCTA TGGCATGGTG ACAATAATGG 540
AGGTTGATTT AAAGTCCTTT GTAAGAATTA AGAGTTATAA TAGACATAAA GTGCTGTATC 600
TGGTATACCT AGAAAACATT CCATAAAAGT TAGTAATTGT TGGTCATGTA ATGATGACTC 660
TCTAGGCTAG GATTTCAGCT TCATTGCATG CACATGGTGC ACTCACAGGG CGTGACCTCT 720
CTCTGTCTCA GTAACCTCAT CTGAGGACCG GGATAATCAT ACCGCTTCAA AGGGATGTCA 780
TAAAGATTAA ATAATATGTG TAAGGCTGCT TGCATTTAGC TGCATTCAAC AAATATTTCT 840
GTATCTTTCT CCTCATTTCT CCTTACTTTC TTGCTTATTA TCTGCTCTAG GTATAGATTT 900
CAGAGAACTA AGCTTGTTAC AATCCTTCAT AAAATAACCA GGTTGGTTAG GGCATTTCCA 960
AGAGTCAATA CTGTTTAGTG ACTATTCTCT GTTTAATCTA TTTTGATTGT CCAGGGTCAT 1020
CTTTTGCTAT GTCATAGGTT GTTGGCTTCT TCTAGAGAAG TGAGACGATG GACAAGTTCC 1080
AAGTGAGTGA GGCGACTGGT CAGGATATTC CGCTGAAAAA CTCATGTCAG TTCTAATTCG 1140
TGATTGTAAT TCAATCACAG CCTGAGAACA GTAGGACTGT AGTTCAAATG CTCTGTTCCC 1200
TTTTTTTTTT CCCAGAGGAT AATTTTTTTT TTTCTTTGAG ATGGAGTCTT 1250
|
