| Tag | Content |
|---|
EnhancerAtlas ID | HS093-00490 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr1:25466340-25467430 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:25467070-25467088 | GGAAGGAAGCCCGGCAGG | + | 6.35 |
|
| | 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 |
| GH01I025140 | chr1 | 25466725 | 25467101 |
|
Enhancer Sequence | CCTCCTGAGA AGCTAGGACC AGAGCCATCC ACCCATGCCA AGCTAATTTT TAAATTTTTT 60
TGCAGAAACG AGGTCTCACT ATGTTGCCCA GGCTAGTCTT GAACTCCTGG GCTCAAGCGA 120
TCGTCCCACC TCAGCCTCCC AGAGTGTTGG GATTACAGGC ATGAGCCACC GTGCCTGACC 180
AAGATCTTTA AATAGTAATA AAACAGACAT TTATTAAGTG CATCTCATGT GCTGTGCGCT 240
GTTCCAAGTG CCTACACTCC CCATCTCAGT TAAGCACACA CCACCCCACG GGCAGGCAGC 300
TGCTATCATT ATCCCTTTCT CATGGTGGGG AAGTGAAGAT CAGAAAGGCT GAATAACTTG 360
CTCAAGATCA CAAGTCTGGA CTTGACTGCA GGCCTGGCTG ATCCCAGAGC CCAGATCAAG 420
AGTCTCCCCT GGTGCCTCTC CCCTAAAACC ACCTCAGAAA CCCCCTGGTG TGTAACTCTA 480
AACCATGCCT GCGGCAAACT CAGCCCATTT CCTCTTCTCG CATCTTAAGC CCAGATGGGG 540
TCTGAGTGAC ACTTATCTCA TACCCTGTCA TAGAGCTGGA GCCCCACAGG AATGTGGAAC 600
TCCCCATGGA CAGAGGGCAG GAGGAAGTGA CCGCCGGCCC GAAGGGGGCT TGGTCCACTG 660
GGTCCAAAGG TGCCGTCTGG CCCTGGCTGC CACATGCCTC GTGTCCACAA AGCAGAAGTC 720
ACAGGGACAG GGAAGGAAGC CCGGCAGGCA GACTGTCATC ACAGGTGGTG TGTCCTCCTA 780
TCCAGGGACA AGCAGAACTA GCCAAGATTG CCTTCTCCAC GCAGCCTCTC CTGATTCCAC 840
ACTTGTGACT TCATGTTCCC AGAGCGCTGT GCTGGCACGT GTGCTATGAT CTTGACTCTG 900
TATGCACCCC GACGCCCAGC TACAAGCAGC TCTACCCTTA CCTAACCTTT AAATTGCTCG 960
ATTGCCTCAT CTGTAAAAAC AGGGATGTTA ATAGCACCTG TTTCACGGGG TTATTGGAAG 1020
GTGTGTGTAC ATACACACAC ACACACACAC TCATCAATAT AGATGAGTAT AGATTGTGTG 1080
TATGTATACA 1090
|
