| Tag | Content |
|---|
EnhancerAtlas ID | HS034-14672 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr19:11128510-11129630 |
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 | GTGACTCCAA CCCTCAGGCT CCTTACCTCA TGGTTGCAGG ACGGCTGCAC TGCCTCCCTC 60
GCCTCATGCA GGAGAGTGGG CAGGAAAGAG TTCTAGGAGA GTGGGCAGGG CAAAAGGCAG 120
CAGAAGCGCA AGGCTGCTGA GCCTCTGCTC CCCACGCTTC TTCAGGAACT CTCCCCAGCC 180
TTCACCACAG CCATGCGTCC TTCTGTCTAT TGGCTGTGCC GCCTGGTTGG CTGTGGCTTC 240
CAGCGGGGCT GGAGATGGGT TCATGGTGGA CACAGCACCT CCCTCGTGGA GCTGCTTGGG 300
GGCAAACCAC GAGTAGTCCC TGGGACTCCA GCTTCGAGCC CTGTCTTTAC GGACCACCCC 360
GTCTAGACTT TCTGAGTGGC TTCCCTCCCC CACTGAAAAC TCCCTGCCCC AGAGTTCCTC 420
CCAGAGCCCG TCCCCTTTGG GACTCAGCTT TATTACCGCC TCCACCCTCT CCTCAGTCTC 480
TAGGCTGTCG GTCTCAGGTG ACTCACCCCT CCCCACTGCA TTCTGCCTGC CCCCATGTCC 540
TCCCTCATTC CAGCCCTGGT CATCCCACAG GGGAACAGCC ACGAGTTGCC GCTCCCTCCC 600
ATCCCTGTCC TCCCGCCTGC CACCTGAGCC AGGCCCCGCC TCGCCCCTCA CTGTCCTCGT 660
TCTCTCTCAC AGTCAGGAAC CTTCCGTGGC TGGAGGGTGG CAGAAAGACT GTTTGGTGTC 720
TCCTATATCC TCAGGTCTCC ACAGCACTGT TGCTAGCCTG GCTCTGGGCG TGAAGCCTGT 780
GCTCTGAAGC TGCATTTTCC CGGCAGCAGG TCCAGGCTTC CCCAGCCCTG GCAGCATTGT 840
TTCTGTCCCC CATCACATCT CTGTGTCCCT ACTTCTCACT CTAAAGGGCC TTGCCCTCTT 900
TTCCCAGTGG CCTCCCTTCT GTCCTCTGAG GCAGAGCCCT TCACGTCCTC GCCAGTCTCT 960
CTTCCTCCCT CCCTCCCTCA GCTGCCCTAA ACACAGTTTC TCTGCCCACT CGGAGGGCTG 1020
TGGCCATGTT GGCCTCGCCC CTGACAGCCA GTGGCTATGG GTTTGCACAG TGAGCCATTG 1080
ATGAGAGACC GGCACTTGAC TCTCATTTCC TTGTTCCATC 1120
|
