| Tag | Content |
|---|
EnhancerAtlas ID | HS012-14101 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr16:57640250-57641450 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Hnf4a | MA0114.3 | chr16:57641096-57641112 | CCTAGACTTTGACCCT | - | 6.64 | | RREB1 | MA0073.1 | chr16:57641300-57641320 | GGGGTGGGGGTGTATAGGGG | - | 6.43 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_20290 | chr16:57638170-57645300 | CD56 | | SE_23045 | chr16:57639876-57641328 | CD8_primiary | | SE_24479 | chr16:57640545-57641346 | Colon_Crypt_2 | | SE_29478 | chr16:57639706-57642696 | Fetal_Intestine_Large | | SE_31472 | chr16:57640003-57645039 | Gastric | | SE_47718 | chr16:57640581-57641457 | Pancreas | | SE_65275 | chr16:57640224-57645423 | Pancreatic_islets |
|
| | 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 |
| GH16I057605 | chr16 | 57639731 | 57645941 |
|
Enhancer Sequence | GCTGGTAAGT TACAGAGCAA GGATTTGAAC TCTGGCAGCC CAACTCCACA GTCTGAGCAC 60
TTAACCCTAT ACATGGCCTT ATAGGCCAAA AATACTTCTG TTAACAGGGA TGACCTGGAA 120
AATCAAGAGT GGAGGGGCAG AGTCACTTTT TAATAAATAC TTCTAAATAG ACATTAAAAA 180
ACACGAACTG GTAAAAAGGA CTTATAGTGA AAAGCCCATT TCCTGCAAGC CCCCTCCCCA 240
GAGGCAACCA CTTCTAATAG TTCGAGCTCA TGTGGCAGTT ACCTCCAGAG CCATAAATAA 300
CATGCTTCTA CTGCCATTTC CTGATTTATT AACCTTGGAC ATTATCTGTT GACTTCTGCA 360
AACACTCAGA AAAGGAAAAA TCAGCTTACC TTTTTTCTCC TTTCTTCTTG TTATGTTGCT 420
TCTTGATAAC AGGGCTGTTT GCTGCCACTG GCTCTGGTCT AGACCCTGGG CTGGACACTC 480
GACTGCACAG TTGCCAAGAC TAGGCCCACT GAGGTTCAAG ACAAAAAAAG GACTTGCCCA 540
AAGTCACTGT GAGTTGGTGT TGGAGGTGGC ACCCGGCTCC TGGTCTGCAT GGCTCCAGGG 600
CCGGGCTGTC TCTGTGATAC CCTTTGGCCC ACCCTGAGAG TGACTCTTGT GCCACCCCTG 660
GCCCACGCGG GCCTCTCTCA CTCTGGCAGA GGCTTAGCAT GGCTGGGGTG GGTGGCCCTG 720
GCTGGGTTCC TGCTGAGGGC TGGCTGAGGC CTCCTGCTCA GGCAGGGGCA GGCATATTTG 780
CAGAGCAGCA GGTGCAGCCT CCCAGTGTTT GGCCAGCCAA GGGTTTTATT CTCCAACACT 840
GCCAGACCTA GACTTTGACC CTCAGGGACT TCTACACAGC TGGCCTTCCA GATCACTGCC 900
CCCATAGCCT CTATATCTCC AGGGGAAAGG CTGAGCCAGT GGCTGAGACT GGCAAAGTGC 960
CGAGCACCAG ATACCCAGGA CCCTTAGGGC GAAACCACCA GACTCACATG CCCCAACCCT 1020
GCAGTCGCCT GGGGCCATCG GGCGGGTGTG GGGGTGGGGG TGTATAGGGG TAGAAGGAGC 1080
TTTAAAAAAT TACCAGTGCT GGCCAGGCAT GGTGGCTCAT GCCTGTTATC CCAGCACTTT 1140
GGGAGGAATA GGCGGGCGGA TCACTTCAGG TCAGGAGTTT GAGACCAGCA TGGTCAACAT 1200
|
