| Tag | Content |
|---|
EnhancerAtlas ID | HS108-38849 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr8:21994340-21995530 |
Target genes | | Number: 20 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr8:21995047-21995066 | TGCTGCCCTCTCGTGGCCA | - | 7.31 |
|
| | 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 |
| GH08I022136 | chr8 | 21994481 | 21995511 |
|
Enhancer Sequence | TTAATATATG CCAGGGGCTT AGAGCAGCGT CTGCGTGGGC AGCCACACTC TGGGCGCCAG 60
CCGTTACTAC TGCCTGCATC CCTGCAGTGT CTGGCAACAT GTCTGGTACC TGCTCGAGGC 120
TCAATAAAGA TTCATTTTTG AATGAATTAA TGAAGCGATA AGACAACCCC ACGATGCAAA 180
GGCAGGCCAT GTTGGACGCC AGTGAGCCCC TATACGTGAG AAGCTAAATC ACCGCAGCAG 240
ATTAAGAGCC TCCCCCAAAT AAAACCTGGA TAATCCCCAC ACCAAGAGTT AATCCACACT 300
CTCTGGGGCC ACTCCAGGTT ACCACCCCAT TTCCCCTCTT CTCATCCCAC ACTCTCACCC 360
ACCTCTTTGC TTAATCAATC AAAAGCAGGG AGGAGGAGCA GGTGCAGCAG TGGCAGAGGG 420
GCGCACCCCG GGCATCATGG TGAGACCAGC ACCGGGGCAG TAGAGGGCAG AGCTGGGTAC 480
CCCGGTTGCC CCAGGGATCG GAGGAGTTGG AGTGGAGCCA GCCAGGCAAA CAGCCTTGGT 540
CTCAGGAGAG CAGAGACTCC TTGGATGGGG CAGGCCAAGG ACCAGTGACC ACAAGCAGCA 600
GGGAGGGCCA CTGAGTTCCG CCAGGCCCAG CAGGGCGAGG CTCTGGCCAG TCTCCCAACC 660
CCACCCTCCT TGACCTGGAA GCCGGGGGCA GCCCAGATCC CAGACACTGC TGCCCTCTCG 720
TGGCCACTCC TCAGAGGTGC AATGGTGCCC CTGCGGGTAC CTGACTGTTT ACAGAACTTA 780
ATGTCCCCAG AGCTGCCCCA GGGGGCTCCT TCTTCCAGGC TCCTGGAGGA GATACTCCTC 840
CCCAGGTCTC CTCTGCCTAG CTTCGACCTC CCTATGGGAC TAACGTGCTG CCCCAAGCCC 900
CTCCTGCCTG TGCTCCCACT GGTTTCTCTA TAGCTGCACC TTCCTGCCAA GGCCTAACTG 960
AAGTTTCGGG TTCTGACCAG TCCTCTGGAC TCGTCCCCAC TTTCCCATCA GTGCTCTCAA 1020
AACTCCCCAA AAGCTCCTTC GTGAAACCAT GTGCTGCATC ACAACTCTCT GTCAATGGTT 1080
CTGTCTCCCC CAGAGGACTG GGCTCCTTCA GCCTTAGACC TAGGCTAGGA CTGGGCTGTC 1140
CCATTTCAAG GGTGTGAGGC GAGCAACGGG AGTAAGAATC AGGAGAAACA 1190
|
