| Tag | Content |
|---|
EnhancerAtlas ID | HS012-20405 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr6:2865760-2867140 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr6:2866596-2866611 | AATTAATCAATAACA | + | 6.08 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_28080 | chr6:2865882-2867415 | Fetal_Intestine | | SE_28996 | chr6:2865858-2867021 | Fetal_Intestine_Large | | SE_38162 | chr6:2865399-2867166 | HUVEC |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 2866705 | 2867019 | | chr6 | 2866631 | 2866750 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I002864 | chr6 | 2865041 | 2867315 |
|
Enhancer Sequence | ATTTTTTGTA GAGACAAGGT CTCACTAGGT TGCCCAGGAT GGTCTCAAAC TCCTGGCCTC 60
AAGTGATCCT CCCACATTGG CTTCCCAAAT TTCTGGGATT ACAGGTGTGA GCCACCAGTC 120
CGGGCCAGAA AGGAAACTTT TTATCTGAGG AATATGAACC CCTTTAAGTC ATCAGGTCCA 180
GACAGGCATT GAAATGTGAC AGTAGTCACA TCTCACTCAC TGCTTGAGCT ATGTATGTAT 240
GTAATCTGCC TGCTATGTGG ACTCTTGACC CAATGCCACC ACCAATAGCT ATAAATTAAC 300
CTAACGACGG CATATGCTGG ACAACATAAC TTATACCCTA TAGTTCAACT ATAGCCAATC 360
ACTAATCAAT GTTATTTCTG TAAACCAATG AGAATTCTTA ACCAACAATG TTGGTAATTG 420
CCTCCTCTCC TGATTCATCC TTTGTTCTCT GGGCACTTCC CAAGACAACT TGGAAGTGTT 480
TCCCAAGCAG CTGTTCTCAA CCCTGACCCA AATAAACTCT CATATTAATT TTGCCTCAGC 540
TTCTTCCTGT CAGTCGACAA CTCCTAACTA GCTATTTTCA TCCCTTTTCA AGCTTCCTAA 600
GAGGTTACTT TCATTTAGGT TCGTGATATA ATAAAAAATA TATCTGGTGT TTATCCCCAG 660
TTCCCGGCAC AGAGCTCCTA AAACCCTTGG AATTTCCTGA GTAATGCGAG TGTGTTTTGC 720
TATTCAAAAT GAGCCGCTTT AGCTACACCT GAGCTTATGC TGATGAGGCG GCTCTTGGTG 780
ATCCCCTGGG GAGGGAAGAA GGGCTGGGAA TTGAGTTCAG CCACCAATGG CCAGTGAATT 840
AATCAATAAC ACCTATGTAA TGGAACCTCC ATAAAAATCA AAAAGACCAG GTTGAGGGAG 900
CATGTGGGTT AATGAACAGA CAGGTGCTGA GAGGGTGGAG TGTCTAGAGA GGGAATGGAA 960
GCTCTCTGCA CGCACCCCCG ACCCCCCTTA ACTTGCTCTC TGCATCTCTT CCACTGGTTG 1020
TTTCTGCCTT TATAATAAAC TGGTGATAAT AATAAAGTGC TTTCTTGAGT TCTGTGAGTC 1080
ATTCTAGTAA ATTATTAAGC CTGAGGGAGG TTATGGGAAT CCCCAAATTT GTACTTGGCC 1140
GGGCAGCAGT GTGAAGAGCC TGGGCACCCC ATTTGTGACA GGTGTCTGAA GAGGGGGTAG 1200
TCTTGGGGGC TGAGCCCTCT AACTGGACGT TAAGTACTGT CAGAATTGAA TTGAATTGTT 1260
GGACACCCAG TTGGTGTCAA AGAACTGATT GGTGTGAGGA AAAAAACCTC TTAAAGGTCT 1320
TTACTCCCAC TTACTGGTAG TGTTGCTAAG TTCATAATGC CTTTTTCTTA TCACTCATGG 1380
|
