| Tag | Content |
|---|
EnhancerAtlas ID | HS145-11522 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr19:11128590-11129630 |
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: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I011017 | chr19 | 11128237 | 11130243 |
|
Enhancer Sequence | CAGGAAAGAG TTCTAGGAGA GTGGGCAGGG CAAAAGGCAG CAGAAGCGCA AGGCTGCTGA 60
GCCTCTGCTC CCCACGCTTC TTCAGGAACT CTCCCCAGCC TTCACCACAG CCATGCGTCC 120
TTCTGTCTAT TGGCTGTGCC GCCTGGTTGG CTGTGGCTTC CAGCGGGGCT GGAGATGGGT 180
TCATGGTGGA CACAGCACCT CCCTCGTGGA GCTGCTTGGG GGCAAACCAC GAGTAGTCCC 240
TGGGACTCCA GCTTCGAGCC CTGTCTTTAC GGACCACCCC GTCTAGACTT TCTGAGTGGC 300
TTCCCTCCCC CACTGAAAAC TCCCTGCCCC AGAGTTCCTC CCAGAGCCCG TCCCCTTTGG 360
GACTCAGCTT TATTACCGCC TCCACCCTCT CCTCAGTCTC TAGGCTGTCG GTCTCAGGTG 420
ACTCACCCCT CCCCACTGCA TTCTGCCTGC CCCCATGTCC TCCCTCATTC CAGCCCTGGT 480
CATCCCACAG GGGAACAGCC ACGAGTTGCC GCTCCCTCCC ATCCCTGTCC TCCCGCCTGC 540
CACCTGAGCC AGGCCCCGCC TCGCCCCTCA CTGTCCTCGT TCTCTCTCAC AGTCAGGAAC 600
CTTCCGTGGC TGGAGGGTGG CAGAAAGACT GTTTGGTGTC TCCTATATCC TCAGGTCTCC 660
ACAGCACTGT TGCTAGCCTG GCTCTGGGCG TGAAGCCTGT GCTCTGAAGC TGCATTTTCC 720
CGGCAGCAGG TCCAGGCTTC CCCAGCCCTG GCAGCATTGT TTCTGTCCCC CATCACATCT 780
CTGTGTCCCT ACTTCTCACT CTAAAGGGCC TTGCCCTCTT TTCCCAGTGG CCTCCCTTCT 840
GTCCTCTGAG GCAGAGCCCT TCACGTCCTC GCCAGTCTCT CTTCCTCCCT CCCTCCCTCA 900
GCTGCCCTAA ACACAGTTTC TCTGCCCACT CGGAGGGCTG TGGCCATGTT GGCCTCGCCC 960
CTGACAGCCA GTGGCTATGG GTTTGCACAG TGAGCCATTG ATGAGAGACC GGCACTTGAC 1020
TCTCATTTCC TTGTTCCATC 1040
|
