| Tag | Content |
|---|
EnhancerAtlas ID | HS109-13046 | Organism | Homo sapiens | Tissue/cell | Kasumi-1 | Coordinate | chr2:172876360-172877610 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr2:172877481-172877492 | AAATCACAGCT | + | 6.14 |
| | | 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 |
| GH02I172011 | chr2 | 172876508 | 172877507 |
| Enhancer Sequence | TTTTGTATTT TTAGTAGAGA CGGGGTTTCA CTGTGTTAGC CAGGCTGGTC TCGATCTCCT 60
GACCTCGTGA TCCTCCTGCC TTGGCCTCCC AAAGTGCTGG GATTACAGGC GTGAGCCACC 120
GCGCCCGGCC TAATCTTTCT GTTTCTATAG ATTTGCCTCT CCTGGACATT TCATATAATG 180
GAATCATACA ACATGCAGTC TTTTGTGACT GGCTTCTTTC ATTTAGCATG ATGTTTTCAT 240
GGTTCATCCC TATTGTGGCA TGTGTCAGTT TATTGCTGTA TAATATGCCA CTGTATGGAT 300
ATATCACATT TTGTTTATCC ATTCACCAGT TTGTGGACAT TTGGGTCATT TCTACTTTTT 360
AGTTCTTATG AATAATGCTA CTATGAATAT TTGTGTATGT GTTTTTCTGC GGACATATAT 420
TTTGTTTTGG TTTTGAAATA GGCTATGTTT AGATGCAGAG GGAAGCAAAG AAACTGGTAA 480
GGATGTGGTA AAATTACCAC ATCCACAAGA CAACGTTTAT TAAGTACTGA AATATTCCTT 540
TATGAAAGTT AACTCTTGCC ATCCCTTTTA TCTTTCACAT TTAGAGTCTA TATTATCACA 600
ACCTTGTTTT TCCTTTGAGT CAGCATTGTG ATCATTCTGG ACGTGGGGTC CCACACACCC 660
TGTCTCTGTC AGTAAGATTA TGATTAAGAT CAAATAGAAA TAGGTCAGGA GAGAAAAGAG 720
CTCCCTGGCC TTATTCTCCT CAAACTAGCT GATGCTCCTG AATACCAACC TCTTTAAGAA 780
TTGATATTTC AAAGGACAAC TCCTCTCTGT GGTCTTCTGT CCTCTCTCCC CTACTTTATG 840
CTCTGTGCAT AGCAGCTGTT CAGGACATCG CCCGAGCGCA GGGGCACTGC AATCAGAAAA 900
GCGAGTGAGG GACACAGCAG GAGAAGGCTG TTCTGGGGCT AGTGAGTGGG AGACGGGACA 960
AACAGCTAGA TAGCAACGTG ATGGCTTCAC CATGGGGTGA AGCGTGGGGG AGAGTATCAA 1020
TTACCTAGAT TTTAAAAAGA GAGCCCTTGA ACACCTCTGT CACTGGTCAC TTTTACCAAA 1080
GCCTTCTAAC TTAACGGAAG GAGATGCTGC ACTTTAAAGA AAAATCACAG CTGCGGAAGA 1140
CAGTCTTGCA AAGCCAGTTT TTGTGGCTTA GTATTTTGGG GTAGCTTGTT TCATGAGGGT 1200
CAGATTAATT TTCTAATGTT GTTTTCTACC TTAATGTTAC TGCTTTAATC 1250
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