| Tag | Content |
|---|
EnhancerAtlas ID | HS048-00008 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:956240-957580 |
Target genes | | Number: 43 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr1:956659-956670 | TGGGTGTGGCT | - | 6.14 | | RREB1 | MA0073.1 | chr1:956659-956679 | TGGGTGTGGCTGGGGTGGGG | - | 6.61 | | SP3 | MA0746.2 | chr1:956253-956266 | GGTGGGCGGGGCC | - | 6.14 | | ZEB1 | MA0103.3 | chr1:957228-957239 | GGGCAGGTGGG | - | 6.14 | | ZNF263 | MA0528.1 | chr1:957173-957194 | GCCCCATCCCCCTCCTCCACT | - | 6.11 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_57930 | chr1:955451-957429 | VACO_9m | | SE_69072 | chr1:955444-963640 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCAGGAGCAG AGAGGTGGGC GGGGCCGTCA CCGGGCCTCG TGTGCTTGGG GGCAGGGCCG 60
GTGCCCCATC GCGCTCCTGC GGGAACCGGG GCTCCCCACC CCGGGGAGGG GAAGTTTCCC 120
TGGTTTCTCC TTCAGGTGCT TCTGGGAGCC CCCGGGGTAG GTACGCTGGG ACCCCCACCA 180
TCTTCTCCTA GTAGGGGCTC GGGGGACCCA GAGCCGGCGC CCGTGTACCC CCAAAACCAT 240
CTCCTGGGAC CAGAAATCCA CTCATTTCCC TCCACGGAGG TGGAGAAGGT GGCAGCTTCT 300
TTCAGACTGG CCGGTGCGGG CTACAGCTGG GCTCCCCCGC CGGCCCAGTC TCCTCCACAG 360
CGGCCAGGGC ACTTTGCCAG GCCCCTGCAG GATTTTCCCG ACTTCCTCCC CGCTGCTCCT 420
GGGTGTGGCT GGGGTGGGGG AAGGCGATGA AAGCCACCAG GCCCTCCCCC TGCCTGGGTC 480
ATCTGCCTCC TGGAGCCTAC TGTTGGGGGG CGTGGAAGAG GCTCTGCCTG CGCAACTGGA 540
GGGGGTCCCT GCGGATGCCG CAGTCCTGAG GCTCCCAGCA GGGGCTGCGC AGTGGACAGG 600
CCAACCATTG TCTCTCCCCC CATCCGGCAG CCCCAGCCCC CCAGATCTGA GGAAGGGGCT 660
GCTTCTCCCG GCTTTGTTCT CAGGGGAGTG CGTGAGTGCG TGGGTCCCTG TCCCCGTGAG 720
GGCCGCCAGG TCGGCTGTAG CCTTTACCAC AGGCCACCGT CAGAGCAGCT GCCCTCAGGG 780
CCCCAGGAGC TGAGAAGGTG GAGGGTGGGG CACCCTGCAC TGCCCAAACT TGATTTCGTG 840
GTTCACAGGC TGCCCTGAGT GCACAGACTG TAGAAGCCCG AGGAAGGGGC GTCTCAGCCC 900
AGCCACAGGG CCAAGCTGGC CCCTTACCCC AACGCCCCAT CCCCCTCCTC CACTGCCCAA 960
GCTTGCTGGG AGGTGGGCCC TGAGCACTGG GCAGGTGGGG AGAAGTGTGG AAGGCAGGCA 1020
CCCCAAGCCA GGTGGGCCCC CTTCCCAAAT TCGGCCTTAG CTGATAGGGA CGTTATTGGA 1080
GCTGGGGTGG CTGAAGTTGG TTAGACCTGG GGGAGGGGAT GTGTTCACAG GTGACGCATC 1140
TCTGAGCGTT CCCGCATGGG CTGTGGTGGC CAGTGTGGGC TTCCCCCAGC TTCCGCCCAG 1200
CGGGCTGACT CAGAGGTCTC CCCACATCTC TGCCCAGGGC TTGAGTCTAC TGTGGACATT 1260
TGCCCTAAAC ACCTAAAGCC CCCAGTCTAG CCCCTTCCCC AGGAGAGGAC TAATGACACC 1320
TACCGCCATG TCCACCCCAG 1340
|
