| Tag | Content |
|---|
EnhancerAtlas ID | HS012-15409 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr19:11128260-11129630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr19:11129469-11129487 | TCTTCCTCCCTCCCTCCC | - | 6.36 | | ZNF263 | MA0528.1 | chr19:11129468-11129489 | CTCTTCCTCCCTCCCTCCCTC | - | 6.71 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 11128494 | 11128769 | | chr19 | 11128784 | 11129324 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I011017 | chr19 | 11128237 | 11130243 |
|
Enhancer Sequence | TCTGTCTCTG GGACCTGTCC CCTCAGTCCC CTCCTGACCC TTGCTCCTGG CTCTTCTCCC 60
TCCCAGTGCA GATGCTCCGC ACACCTCCGG CTTCTCCCTT GGTGCGCTGA CTGTCCCCAT 120
CACTCCAGGG AGGTTTCACT GTTCCTGAGT CAGCGGAAGC ACAGGGTCAG GCCCTACGGG 180
CCAGGTCCGG TGGCTCCAAG ATGCCATCAG GGACCCAGCC TCCCCCAGGT TTCTGCCCAG 240
TCATTCTTGG GTGACTCCAA CCCTCAGGCT CCTTACCTCA TGGTTGCAGG ACGGCTGCAC 300
TGCCTCCCTC GCCTCATGCA GGAGAGTGGG CAGGAAAGAG TTCTAGGAGA GTGGGCAGGG 360
CAAAAGGCAG CAGAAGCGCA AGGCTGCTGA GCCTCTGCTC CCCACGCTTC TTCAGGAACT 420
CTCCCCAGCC TTCACCACAG CCATGCGTCC TTCTGTCTAT TGGCTGTGCC GCCTGGTTGG 480
CTGTGGCTTC CAGCGGGGCT GGAGATGGGT TCATGGTGGA CACAGCACCT CCCTCGTGGA 540
GCTGCTTGGG GGCAAACCAC GAGTAGTCCC TGGGACTCCA GCTTCGAGCC CTGTCTTTAC 600
GGACCACCCC GTCTAGACTT TCTGAGTGGC TTCCCTCCCC CACTGAAAAC TCCCTGCCCC 660
AGAGTTCCTC CCAGAGCCCG TCCCCTTTGG GACTCAGCTT TATTACCGCC TCCACCCTCT 720
CCTCAGTCTC TAGGCTGTCG GTCTCAGGTG ACTCACCCCT CCCCACTGCA TTCTGCCTGC 780
CCCCATGTCC TCCCTCATTC CAGCCCTGGT CATCCCACAG GGGAACAGCC ACGAGTTGCC 840
GCTCCCTCCC ATCCCTGTCC TCCCGCCTGC CACCTGAGCC AGGCCCCGCC TCGCCCCTCA 900
CTGTCCTCGT TCTCTCTCAC AGTCAGGAAC CTTCCGTGGC TGGAGGGTGG CAGAAAGACT 960
GTTTGGTGTC TCCTATATCC TCAGGTCTCC ACAGCACTGT TGCTAGCCTG GCTCTGGGCG 1020
TGAAGCCTGT GCTCTGAAGC TGCATTTTCC CGGCAGCAGG TCCAGGCTTC CCCAGCCCTG 1080
GCAGCATTGT TTCTGTCCCC CATCACATCT CTGTGTCCCT ACTTCTCACT CTAAAGGGCC 1140
TTGCCCTCTT TTCCCAGTGG CCTCCCTTCT GTCCTCTGAG GCAGAGCCCT TCACGTCCTC 1200
GCCAGTCTCT CTTCCTCCCT CCCTCCCTCA GCTGCCCTAA ACACAGTTTC TCTGCCCACT 1260
CGGAGGGCTG TGGCCATGTT GGCCTCGCCC CTGACAGCCA GTGGCTATGG GTTTGCACAG 1320
TGAGCCATTG ATGAGAGACC GGCACTTGAC TCTCATTTCC TTGTTCCATC 1370
|
