| Tag | Content |
|---|
EnhancerAtlas ID | HS012-18400 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr3:123128030-123129340 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr3:123128450-123128463 | AGGAGCAGCTGCA | - | 6.15 | | ZNF263 | MA0528.1 | chr3:123129158-123129179 | TCCCCCTCCTCCTCCTCCCCC | - | 10.05 | | ZNF263 | MA0528.1 | chr3:123129009-123129030 | GAATGAGAAAGGGAGGGAAGG | + | 6.09 | | ZNF263 | MA0528.1 | chr3:123129184-123129205 | TTATCCCCCAATTCCTCCTCC | - | 6.28 | | ZNF263 | MA0528.1 | chr3:123129193-123129214 | AATTCCTCCTCCTCCTCCTCA | - | 6.38 | | ZNF263 | MA0528.1 | chr3:123129196-123129217 | TCCTCCTCCTCCTCCTCAACA | - | 6.6 | | ZNF263 | MA0528.1 | chr3:123129190-123129211 | CCCAATTCCTCCTCCTCCTCC | - | 7.01 | | ZNF263 | MA0528.1 | chr3:123129187-123129208 | TCCCCCAATTCCTCCTCCTCC | - | 7.21 | | ZNF263 | MA0528.1 | chr3:123129152-123129173 | GTTCCATCCCCCTCCTCCTCC | - | 7.29 | | ZNF263 | MA0528.1 | chr3:123129155-123129176 | CCATCCCCCTCCTCCTCCTCC | - | 8.95 |
|
| | Number of super-enhancer constituents: 14 | ID | Coordinate | Tissue/cell |
| SE_01550 | chr3:123127988-123129579 | Aorta | | SE_03867 | chr3:123128825-123146146 | Brain_Anterior_Caudate | | SE_04971 | chr3:123128740-123149524 | Brain_Cingulate_Gyrus | | SE_05846 | chr3:123127963-123154367 | Brain_Hippocampus_Middle | | SE_07929 | chr3:123128250-123134602 | Brain_Inferior_Temporal_Lobe | | SE_26038 | chr3:123127784-123136151 | Duodenum_Smooth_Muscle | | SE_26748 | chr3:123128718-123129516 | Esophagus | | SE_40589 | chr3:123127759-123154640 | Left_Ventricle | | SE_42153 | chr3:123127874-123129586 | Lung | | SE_46690 | chr3:123128738-123128936 | Ovary | | SE_47869 | chr3:123128079-123128765 | Pancreas | | SE_47869 | chr3:123128797-123129425 | Pancreas | | SE_48554 | chr3:123128036-123129657 | Right_Atrium | | SE_54494 | chr3:123127664-123146810 | Stomach_Smooth_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 123128274 | 123129234 | | chr3 | 123128765 | 123129151 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I123409 | chr3 | 123127455 | 123134665 |
|
Enhancer Sequence | TCCCCATCTG ACCTTGGGTT TTTAGAAAAG TTTAACCCTT ATAAGGGTCT GCTTTAACTA 60
TATCCACTCA ACACCTAGTT CCTCTATGTG CTAGGGGCTG TGCTAGGTGC CATGGGGGCC 120
CCCAGGGATT GGTAAGAGTG AGTCCCAATA CTCCAGGTGT GTACAGTCGC AGGCCATGAA 180
ACCAGGTAGC ATGTGGGGAA AAAGGACAGA CGGCCCAGCA CATGCTAGTT CTCAGGGTGG 240
CCACTGGAGA AGGTATCCTT GGAGTCAGGG TCTAAAGGTG GGATGCAGCT TTCACAGGTG 300
GAAAGGATGT GTTCCTGCTA ATAGTCCTGT CCAAGCAGCA CAGATAGGTA AGGGAAGCAC 360
CACCAAAAAT CCTCAACTGA TTATCTAGCA CAGTGGTTCT CCAAGTGGGA TATCCAGAGC 420
AGGAGCAGCT GCAGCATCAC CCAGGAAGCA GCTAGACATG CAAATTATTG GGCTCCACCT 480
CTGACCTTGT GACTCAGAAA CTCTGGGAGC CCAGCAAGCT CTCCAGGAGG TTAAGATGCC 540
CACTCATGTT GAGATGCCCC TCTTGCACCT CACCTGCTTC CTTAACAGAG GCCGGGCAGA 600
AGGTAGAAAC TGCCCCAGAG ACATTCCCTC ACTCACCGGC CCCTCCCACC CTCCAAGCCC 660
CAGTTGGATG AGCTGAGAAA GTTCCCTGTG GTTAGAGGAG CTAATCTATC ACCTGGATAT 720
AAATTAACTT GCCCTCTCTC GTCACCAGCC CACTGACCTG GGAAAGGCAA ACACGCAGCT 780
GGCAGGGAAA GAGCAGTAAT AAATCTCTTT TTCTACAGGT CCTCCCACAC CCACTTCCCC 840
AACTGAGACC TGTGTTCCCT GAGGCAGTGT GGCCCCATAG CCCTGAGGTC CCTCTGCTCT 900
CCCACATGAG CAGGTGCTGG ATCCGGTCAA CCCAGTGAGA GGCCCCCATC TGCCCTCAGG 960
GCCTCCACCA GAACTAGGAG AATGAGAAAG GGAGGGAAGG ATGGGGGCTG GAACACAGCT 1020
CATCACCCTT AAGGATGGCA GAGTGACTGG AAGCTTCCCT TGTAGAACTC CTCAGGAAAC 1080
AGCCCACAAA GACTCCCTCC AGGGCAGCTC TGTCTTGGCA GAGTTCCATC CCCCTCCTCC 1140
TCCTCCCCCA ACCCTTATCC CCCAATTCCT CCTCCTCCTC CTCAACACAG CAGCCTGGGG 1200
CCACCCCGTA CCTCCCAGGC ATAAGTAGGA ATGGTAGAGC CATATCCCAA GGTGAACTGC 1260
CTGTTGGGGA AGGGCTAATC TCCTATTATT CCAACACCCT TGGCCACATC 1310
|
