| Tag | Content |
|---|
EnhancerAtlas ID | HS108-14865 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr16:22959340-22960580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr16:22960347-22960365 | CCTTCCTTCGTTCGTTCG | - | 6.47 | | EWSR1-FLI1 | MA0149.1 | chr16:22960339-22960357 | CGTTCATTCCTTCCTTCG | - | 6.53 | | EWSR1-FLI1 | MA0149.1 | chr16:22960343-22960361 | CATTCCTTCCTTCGTTCG | - | 6.78 | | EWSR1-FLI1 | MA0149.1 | chr16:22960539-22960557 | GGAGAGAAGGAAGGAGGG | + | 7.09 |
|
| | 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 |
| GH16I022948 | chr16 | 22960201 | 22960350 |
|
Enhancer Sequence | GGTGGAGTCT CCTCCTTCCC CAGCATTCCG CGGGACTGGG AGGACTTGTC GTGGCCTGGC 60
TTCCAGAGCA TGCCTTTTGG CATGGCCGAT CCCCAGCGGA CCCTCCACCC CGACCGCACT 120
GCACTCAGGG TCGTGCAGGT CCAGCACTCC AGTCCTGTCC TCCCCGGGTG AGGATTGATC 180
CCGGCGCTTC CCTCAGCCAC CTCTGTCGAG AGATGCAATT TACCACCAGC TCGGAGGTCA 240
CCGTAGAGGA ACCCGGCCGC CTGCAGGCGC TTTTCTGCTG CTGCAAAAAC CACTGAAAGG 300
GCCACTTTGT GAGCCGCAGC GCTGCTTTCA CAATCAGAGG AGCAGCCATG GGTCCGCAAG 360
CTCTGGAGCC TCCTTGCGAC TCCCCAGTAG GCTCGAAATC CCAGAAACCT CGGCTGCACC 420
CCGCTCCGCG CATTCAGGAG AGGCTATGCC AGGACTGGCG GGCAGAGCGC AGCCTGCACG 480
CGCGCCCCAT GGCGCAGGAT GGGGAGGAAG ACGCCACAGA GACCTGCCGA CACTCGTCAT 540
CCCTAAGCTG CCTGCACCCC TGCTTTGGGC CAGGCATGCC TGAGCGACTC ACTCCCCTTT 600
CGATCTTTGT ATTAATAGCA GCTCTGTGAG GGAGCAGGTA CTGTTACTAT CGTGCCCATT 660
TCTCAGAGGG CAAAACTGAG GCTCTGGGAA GTTAAATGAC TTTCCGGAGG TTTCTCAGCA 720
GGAAGGAGCA AAAACCTGGA TTTAAACTCG AATAGTTCAA CTCCAGAACC AATGGTTTTA 780
AGGTAATCCC GGGTGACTCC ACAGCACCCA CAGTTTGATA AAGATAAAGT CACGATTTCA 840
GCCTCAAAAG CCAACTGCAC AGGGATCATG CGCCACGTGG CTTAACAGCA ACAAAGGTGA 900
CAGATCCTTG GCCATAAGCC CTTCCCACTC TGGTCGCCTG TTCAACTGCG CCACCTACAG 960
GTTGAGTTGC TCACTGTTTC TTTGGAGCCA CATGGAGTTC GTTCATTCCT TCCTTCGTTC 1020
GTTCGTTCAT TCATTCATTC ATTCATTCAT TTGACGTGTC ATTCCACAGA CATTTATTAA 1080
TTTCTGTTCT GAGCCAGGAG CACGGAACTG GGCAGGATGC TGGGGTACAA AAGATGTCTA 1140
TAGTCTAGCA CAGGAGACAG ACAAACTACC ATAATACAGG ATCAACTGAT AGTGAAAAGG 1200
GAGAGAAGGA AGGAGGGCTG CCTGGAGGAG CAGTCTTTTC 1240
|
