| Tag | Content |
|---|
EnhancerAtlas ID | HS182-07804 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr15:101563550-101565000 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MSC | MA0665.1 | chr15:101564351-101564361 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr15:101564351-101564361 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr15:101564351-101564361 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr15:101564351-101564361 | AACAGCTGTT | - | 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 |
| GH15I101022 | chr15 | 101563184 | 101565491 |
|
Enhancer Sequence | CCATCCATAA ACTTCTTAAT CATCTTGCTT TCCATTCAGT GCCAGGCAAA TGGAAATGAA 60
CATTTTCCTG TTCATGTAAC AGAGAAAAGA GCCATGGACT GTTGGTGGGA ACTCCATCCC 120
TGGAATAGAG CAGGGGCAGT TAGCCCTTTC TCTGAGCTCG GGGAACGAAC ACACATAGAT 180
AAGGCCATCC TCATCAACTG TATTTGGATT TCTGCCACCC TGTGATTCCT CGGGATCCAA 240
GGGGCAAGAG GCTGCTTCAC TGTGGAAAAC TGAGGAGGCT TGAGATCCAG ATGGTCCATG 300
ATTTTCCCCC AAAGCTCCCA CGCACAGTGC CAACCAAACA CTGCAGCTTC TTCCACACAC 360
AACCACTTTC CAAACCTGCT TTGAAAAAGT AGGCATTGAA GCTGTGCATC TGTTCTAACA 420
CGAACTTGGA AGCTGGTCCT CCAAGGGGTG AAGCGCTGCC TGTTGGGGCC AGAACAATCA 480
AACACGACAA TCAACGCTAG GCCAATCCTA GAACATTCCA GGAGCAAATC TAGCTGACTC 540
GAGTCTGAAG GTTCTCTCCA GGAACCAGAA TCCTCTGCAT TCTCTCCAGC TTTGCCTTTT 600
TCTTAACAGT TATGCAATCT CATTTCTTCT CTTAGCTTCC TCTAGCTGAG GCCTGAGGGG 660
TGAATTCGTG CTTCTATTTT TCCTGACCTT CACCCCCACT TCCTTTCTGC GATGATTAAA 720
ACCCCCTACC CTTTAGTGGA AGGACAATCC TGTGAAGGCT GAGCCCGCCG CTCTCTCTGT 780
GGCCGGCCTC AGCCAGTTGA GAACAGCTGT TTTCATCTTT ATACAAAACC AGGTCAGCAC 840
ACTGTGTCTT GGAGGCTGAT GCTGCCTCAC AGAGATGACT CCTTTCTGTA GAAAACTGCA 900
GCCTTAGCAT CCAGGGCCAG ACTCTTACCT CATGCAATGA TAGAGAAACC ACCGTTTACA 960
CAGCCGTTCC CGGCAGCCCA ACAGCTCATC TTTTGTTTGA TTCCCACAGG GTGGGAGGGA 1020
GTTTCCCAGC ATCCTTGGTG GGCGCCACCC TCTGAGCCCC ACAAGTTCAG AGGCCCATCT 1080
CCTCCTCTTG CCCTGGCACA CAGGGAGGCT GAACCCCAGT GCAAGCCGTG ACATCAGAGC 1140
ACAGCTTCCT CCCACAGGGC ATCCCCTACC CATCTGCAGC CCAGACAGAG CCAGGCCCTC 1200
TGAAGTCTGT CCAGGGCCTG GTCTCTGCTC TGCTAGGAGT AGACAGAAGT CCCAGAAGCC 1260
CACCCCCATG CCACCGGGCC CCTGTCCCTC GCCCAGATAA CTGTTTCCTA AGAAACAATA 1320
GAGTGTCCAG AACTTTTCCA CGGTTGTTTT TTCAGACCCC CGAGTCCAGC CTCCAGAGTT 1380
ATCCGTTGTC TCCGTTTGAT TGACTGAAGC CTTTGTCTCT AAAATGCCTC CCTGTCGCTG 1440
CCTTGTTGCT 1450
|
