| Tag | Content |
|---|
EnhancerAtlas ID | HS012-22836 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr8:28199750-28200450 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Hnf4a | MA0114.3 | chr8:28200040-28200056 | CTTAGACTTTGACCCT | - | 6.89 |
|
| | Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
| SE_10187 | chr8:28193185-28199915 | CD19_Primary | | SE_10881 | chr8:28188182-28210367 | CD20 | | SE_27701 | chr8:28198699-28202802 | Fetal_Intestine | | SE_28577 | chr8:28197992-28203262 | Fetal_Intestine_Large | | SE_40988 | chr8:28198227-28199833 | Left_Ventricle | | SE_52497 | chr8:28199865-28201111 | Small_Intestine | | SE_58992 | chr8:28165452-28207351 | Ly3 | | SE_59946 | chr8:28164768-28207284 | Ly4 | | SE_61002 | chr8:28174118-28277761 | HBL1 | | SE_63042 | chr8:28186067-28207603 | Tonsil | | SE_65386 | chr8:28199304-28202459 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TCCCAGCTAC TTGGGAGGCT GAGGCAGGAG AATCGCTTGA ACCCAGGAGG CGGAGGTTGC 60
AGTGAGCCGA GATTGTGCAC ATTGCACTCC AGCCTGGGCA ACAAGAAAGA AACCCCATCT 120
CAAAAAAAAA AAAAAAAAAA AAAGAACACT ATTCAGAAAG TGTAATGATG TCCTAGGAAG 180
GAAAGGTGTT GGGGTGCAGG CCCACCTCTA GACAGAACTT GTCACAGCTG GTCTTAGGGT 240
TCTGCCTTCC TTTCCCCTGA CCCTATACTA CCTTCCTCTT TTCTGCTACC CTTAGACTTT 300
GACCCTTCTA GGCAATGGAA ACTGAGCACA TTCATTCGTG GTCAGGTTAT CAGTGCCATC 360
AGGCTCAAAG AGCACTTGCA AAGAAAAGAA CTGTAAAACA AGGGCACTAT TTCGCATGGG 420
CTCCGAATAC CAGCAAGAAC TGTTCCCCGG GAAGGGGCTT GCCACTGTGC CTATCGAGTC 480
ACAGCCTACA GACCTCCCGT TTAGTCTATT AGTCCAGCCA GTAGACCCGG GGCTGGGGGA 540
GCAGATGTGC GGAGATGCTG AGGACCCCTC TGGCTACGTT AGGAACGATT TACTTGGGTT 600
GATAGCTTTT CTTTGCCTCC CTTTCACTGC TTCCGTCTCT AGGGGGAATA GAAAAGGGTC 660
AGAAAAACCA TCAGGTTTGC CATTTTTTAA CCATTTCTGT 700
|
