| Tag | Content |
|---|
EnhancerAtlas ID | HS012-14214 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr16:75343680-75344870 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr16:75343994-75344011 | AATGTCACAATGACATT | + | 6.02 | | Foxa2 | MA0047.2 | chr16:75344510-75344522 | TGTTTACTTTGT | + | 6.18 | | HNF4G | MA0484.1 | chr16:75344097-75344112 | TGGACTTTGCTCTCA | - | 6.41 | | SCRT1 | MA0743.1 | chr16:75343881-75343896 | ACCCACCTGTTGCAA | - | 6.7 | | SCRT2 | MA0744.1 | chr16:75343883-75343896 | CCACCTGTTGCAA | - | 6.39 | | TCF7L2 | MA0523.1 | chr16:75343899-75343913 | AAAGTTCAAAGAAA | + | 6.23 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28243 | chr16:75337321-75345603 | Fetal_Intestine | | SE_29161 | chr16:75337343-75345706 | Fetal_Intestine_Large |
|
| | 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 |
| GH16I075303 | chr16 | 75337402 | 75345344 |
|
Enhancer Sequence | GCACTCCAGC CTGGGTGACA GAGTGAGACT CCATCTCAAA AAAAAAAAAA AAAAAAAAAA 60
AAACCAATCC AGTTCCAGAC CAACAGAACC ACTGGTTTCT TTGTTCTTTA TCCTAAGCCA 120
TAGGGCAAGG TACTGCCAGA AAGTCTGCTT TAACAGACCA CTCTCCAGAC AACAGTACTT 180
CATTGAGTCA AGAGACTCCT CACCCACCTG TTGCAAGTCA AAGTTCAAAG AAATGCACCA 240
TGCACTTGCT CACCCAGATT ACATCCCAAA TGTTACGCTG AGGCATTCTG GAATGTTATT 300
ACCAAGATGT TTCCAATGTC ACAATGACAT TGCAACCACC TCCTCCTGAA CATCACATGA 360
CTTTGTTGAC CTTACTACCA TAAATTTGAT GTAAAGACTA ATACTGTTCA AGGAGTGTGG 420
ACTTTGCTCT CACCAGCCAG CTTCCATGCC ATAAGAGAGA GTGGCTGAGT GCAGCTCATA 480
CTGGTGAAAG AGACACTTAT TTTCCAAGCT TATCTTTCTT GCATATTTTG TTCAGTTATC 540
CATCAATCAG CAATTATCAA CTCCCTTCCC ACCATGCCAA ACCAAGACCT ATCATAACAC 600
CAGACACCAA CCAAGACCTT GATTAAGAAA CTCAGAAAAG TAAAAGAGAC ACAGAATGTA 660
AAATGACAAG TCATCTTTTT CTTTTCTAGG TTCAAAGTTT ATAATGATAA TTTTCTAGAA 720
CTTATTCTGC TTCTCTTTAG CAAAAGAAAT GTAATTTTAA CAAAAATGTC ATTGTAACTA 780
AACAATAAAC TTCATCCTGT TGAGTCTGTC ACAGAGATAT TATGGTAACT TGTTTACTTT 840
GTTCCATGTC CACCAGCATT GACTTGGATT TGTCCAACCG ATTTATTTTG TAGCAAGAGC 900
ACTGTTCTAT CTGACCACCC TCAGCAATGC CCGGGATCCT GCTGTTTGTT TAAAAGAGGT 960
ACTGGAAAGG AGCTGGGAGA GTAACTTGCC AAGTGGAAAG GCTGACAGGG CTTACCAACT 1020
GTTTGTGAAG GATGGTAGAA GATCTTTCCC GGAGATCTTT AAAATCATCC CCAGGTACCC 1080
AGCTGTTTCA CAGAATAGAA TTTTAGCTTT GGAAAGGAAT TCAGAGTCAT TCATTCATTG 1140
CATTCATTCA ACAGAGATTA CTGAGAACTT ACTCTCTACC AGACACTGTG 1190
|
