| Tag | Content |
|---|
EnhancerAtlas ID | HS108-41189 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr9:111756580-111757690 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr9:111757385-111757396 | GTTTGTGGTTT | + | 6.02 |
| | | 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 |
| GH09I108994 | chr9 | 111756481 | 111757880 |
| Enhancer Sequence | GGCTATTGTA TCAATTGTGG GTGTGAAATA GTAGGGACCT TACTAGTATA GTAGCCATAG 60
GAACATTAAG AAGATGATTT GGGAAACATT AAGAAAACAC AAAATTAGTA CCTGACCAAT 120
GATAAGAAGG AAAGAACGAG TAAAAAAATG GCCTCAAAGT TGTAAACCTA AGTTGCTTAA 180
AGAAAATCGA AGGGCATTGG AAGAGAGATG ATAATTTTAC TGTCAGACAA CAGGAGTTTG 240
AAATAACACA GGAATACACC AAAGATAAGT CGCAAGACAT GGACTGGTAA TGCAGACTTG 300
GATGTCTTGT GTATAATGAC AATAGCTGAA GCTCTACAGA TAGAGGAATT CTGTGGTAGC 360
CAGCCTTCAA GATCGCTCCC CATGATCCCC ACCTACTGTT ATTGACAACC TTGTGCTGTC 420
TGTCCCCTCC CACATCATAC CAGGGTTGGT ATGGTGGAAG TGGTGGTATG TCACTCCCAA 480
GCTTAGGTTC TAAAATAACT GAGGCAGCTG TCTGGGTTGC TCTCTCTCTC TGAGAGAAGC 540
CAGTTGCCAT GTCATAAGCA GCCCTTACTA CACAGATAAC TACGTGGAGA GGAAGTGAGG 600
CCTCCAGCCA ACAGCCAGCA AGGAAGTGAA GCCTGCCAAC AACCATGAGA GGGAGGCTGG 660
AAGCAGACCT GCAGTGCACT CAAGCTTCCA GGTAACAGAG GCCTGGTCAA CACACTGACC 720
GCTACCTCAT GAGACACACT GACCCTGAGC CACCCAGTGA AGCCACTCCC TGATTGGTGC 780
CCTCTCAAAA ACTGACATAG TAAATGTTTG TGGTTTTAAG TTGCTAAGTT TGGGTTAATT 840
TGTTACACAG AAATAGGTAG CTAATACAGA GTTTTCATAG CAAAGAACAG AGAACAAAAG 900
TGCTTAGAAT TAACCTTAAG GCATACAGAA AGGGCAGGAG GAAAAGTATC AGTTTGCATC 960
CTATCATTAA TAGCTAAAAG GATAAAAATG TTTCCTCTGA TCCTCTGGAA AATGTTAATT 1020
TTTTTCTACA CCTCTCAACC ACAAAGGATA CGACATATAA GCCTGCACAT ATGGCATTAT 1080
TCAACCTTTC CTTTTTCTGA CTAGACCCCA 1110
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