Tag | Content |
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EnhancerAtlas ID | HS108-23888 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr2:190329980-190331150 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nkx3-2 | MA0122.3 | chr2:190330531-190330544 | ATTAAGTGGTTGT | - | 6.32 | Nkx3-2 | MA0122.3 | chr2:190330394-190330407 | ATAACCACTTAAC | + | 6.87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I189465 | chr2 | 190330361 | 190330450 |
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Enhancer Sequence | GTAATACTAT CTGTGTAGCC ACTTAATTTC AAAGTATAAA ATATTTCACT TCCCATTTTA 60 CAGTTTCAAT TGTCTTTAAG ATGTTTCATC TTGACAAGGT TTAGATTTAG AGATATGGGA 120 GAGGTTTTAT TCTAATAAAA CCTTTAAGCT TTCTGCTCTG AGAAGACATT GATGTCCTCT 180 AAGTCATAAT GTCATCTCAT AATGAATAAA GAAACATGGA AAAGTGACAC CTCCTCAAGG 240 GCATAATACC GAATTCTAGG CAAATCCAGG GTTAGAATCC AAATGTTCCC TTGCTCTTCC 300 GTTAACAGCA TACTGCCTTT TGAAAAGAGG GAGTGTAGGT AGAAGTGTAG CATAGTATAA 360 TGTAGCATGG ATGTTGTGAT TAGATAAGGA ATCCACTCTC GTACTGTGGC TATAATAACC 420 ACTTAACAGA TCTTTGCTGT GTGCCAAGAA CTTGGCTTAG AGCTTTGTAC CCATTATCTT 480 ACTCTTCAAA AGAACACTGT AAGATAAGCC TGTTGTCTAT ATTTTATAGG TGAAGAAACA 540 GGCCCAGAGA GATTAAGTGG TTGTCCCTAG TCACTGTTGT TATAACTTGT GCTTTTTTAA 600 AATCACAATC CTATGCTGCC TTGATGTTCT TTTAAGAACA CAGTCCTAGT TGTCTTTCAT 660 TCACAGCGTT GCCCTCTAAG CTCGAAATAA GCTTTAAGAA GTCATTTAGG TGACTAAAAA 720 TAGTAAATAA TGACCAGCCA GTTTGACTAA GTAGTTTCCT GTCTATTTTT CCTTGCCCCA 780 GGTGGGGCGT TTCACGGCCT TTCCATTTTT TATTTTCAAA AGTAGGCAGG AATCTGGGTT 840 CTATACAAGT TTCCTACAGA GTTTGATACA GTAGGCTTTT GAGTATCATT GATTGGTGAC 900 CTGTATTATC CTCATTTTGT ACCAATGTAC TAGTGGGTTG ACTACTACAC AGAATGTTCT 960 CTAAAGTCAC ACAAGGGCAA AGGTGATATA TTAGAACTCT TTGCGTCCTG TGGCCATTAG 1020 AGGTAGAGCA CTCAATTGTT TGTCATTCTA CGTGATTATC AGTTGCCTGT TGTTCAAGAT 1080 GCTATTGTAA AATGTACAGC ATGTCAGAAA TTCTTATATA CATCACTTTG TCCTCATGCA 1140 AGAATAAATT TGTGGTTTCC TTCCCGCTAG 1170
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