| Tag | Content |
|---|
EnhancerAtlas ID | HS042-19456 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr17:43925610-43927580 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr17:43927270-43927283 | AGGGACAGCTGCC | - | 6.48 | | RREB1 | MA0073.1 | chr17:43925797-43925817 | ACCCACCACACCCCCCATGC | + | 6.22 | | STAT1 | MA0137.3 | chr17:43926641-43926652 | TTTCCCAGAAA | - | 6.02 | | STAT3 | MA0144.2 | chr17:43926641-43926652 | TTTCCCAGAAA | - | 6.32 | | Stat4 | MA0518.1 | chr17:43926638-43926652 | CTCTTTCCCAGAAA | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr17 | 43926930 | 43927012 | | chr17 | 43925931 | 43926004 | | chr17 | 43926736 | 43926811 |
|
Enhancer Sequence | GCCTATGTCA GGTGATTGGC ACAATGCCCT GCCTGTCCGA AGAGCCCCCT GCACGTGAGC 60
TATGTTTATA TTGCTCCCCT AGTGAAAGCC TCACAGACTC AAACCCAGCT CCTACAAGAC 120
CTTGAGGTCC CAGCCCAACG GCCCTCTTCC ACCCCTCCAA ACCCCTACCG CCACAAGCAC 180
ACGCCAGACC CACCACACCC CCCATGCTTT TTCCTCTTCT TGGAACTCTC TTTCTGCCCC 240
TTCCTTACCA CGCCCCGTGA ACTTGGCCTG GCTGGCTGCT CCTCTTCGCA GCCTTTCCTA 300
AAGCATCCCT GTCTCAATCA CACGACCAGG CACCTTTAGT TTTCCGATCT TCCCCGGTAG 360
AGGGCCAGCT TTGGAAGGGC AGGGGCCTTG CCCATCTTGT TCATCTGTGT AATTTCAGGG 420
CTCAGAACAG CCCCTGGAGT GTTACAGGTG CTTGATGTAT TTGCTGGAGG AATGAACGGA 480
TGGATGAATG AATGAATGAA TGAATGAGGA GTTGACCAGC CTGAACTGCA GAGGAGGGAA 540
TGCTATGAGG GAAGGCCCCA CTGCCCAGGC CACCTCACAG GCTTCCTGCA GGACCTTGGT 600
CAGTGTTGAC GTGAGACTTG GCAGGCCTGG CTGGGCCCTG GAGTGGGGAG AGAGTCCCAG 660
GGAGGCAGTG CAGGTGGTGG GCCTCTCAAA GCCCCGCTTG CCAGGGAAGA AGTGCAGCCT 720
CTCGGTACAC AGCAGCTGAA GGCCCGCTAG ACAAGGGAAG CTTGGAGAAC CCGGCCAGGC 780
CACTGCGGAG GTGTTGGCAG CCCCTCCCAC CGGAGCAGTG GCCATCTGGC CTGGACAGAG 840
GGCCCTCCGC AGGCCCTGGC TCAGCCCCAG CCTGGGCAGC CTCCCTGCTG CTGGCCTGCG 900
TCACGGGGCC TGCCGAGGGC AGCTGCACCC TCTGCCAGGC CCGATGGGAA GGGCTGGACA 960
GAGCCGAGGC CTCCTGGGCT CCCTGGCCCC CACATCCCCC AAAGCAGGAG GTCAGGATAA 1020
AGGAACTTCT CTTTCCCAGA AATCCAGTCT GAGGGCTCTG AGGATGCAGG CCTGGAGCTC 1080
CGCAGGCCTG CAGGGAGGCC AATGCCTACC TCCAAGGAGA GGGGATTCAG GGAGGGTCTG 1140
GGTCAGGAGG CCTCCCCCTT CCCGGCATCC AGACCTGATG GGGAGGTGAG GGCCCACACG 1200
GCCTGGATCT GCTGCCTCCA TCCCTCTTCC CCAACCCCCA GCTTGCTGCA CTGTGCTTGG 1260
GCAGCAGAAC TGAGGTGCTC ACAGGGTCCC AAGGCCAGGC CTGGGGTGGA CAGCAGCCCA 1320
GGGTGCAGTG GCATCACAGT GCCCAGGTAG CTCTCAGCTC TGCTTCTCAC TGGGAATTCG 1380
TCCTAGTCAC CTAAGTTTCA CCACCCCCTC CCCCTGCTGG TTCCCTAGTG TGGCCACAGC 1440
CAGGACTGAC CAATGTCGGG GACCTCTATG AAGGACACCC CAGCTCCAGA GCTCCCGAGG 1500
GCTCACTGGG GCCCCAGCCA ACCGGCCCCG AGGCCCAGCT TCATCCTCAC CTTCCTGCAG 1560
ACCTCACTCC CTCGCAAGCA TCTCCCCTGA GACCACTGCC CAGCACCTCC CACCCAGCAT 1620
GCTCCTGAGG TTCATTCCCA GGGAGCCCAA GCTAAGACAC AGGGACAGCT GCCTTCTACG 1680
TGTGAACTGG AAAAACTATG TGAGTCCCCC CACACACCCC TACATCCTCC AAGCTCTTCT 1740
GCCCTGCTCA GGAAACAAGT GTGGAGACGG GGCTGGAGGC AGGTGATGGG CAGGACCTTT 1800
CTTCTTCCTC CCAAGAATAC TCTGCAGCAA CTCTGCCCAT TTCACAGATG GGGCTGGGCA 1860
AGGACTCTGG GTCTAGAGGC AGCTTGAGGG TTTAGAAAGA GGCACCCAAG CACGGCTGCA 1920
GGTCAGAATC ATTGGGGCAC CTGCCAAAAA TCTGGATTCC TGGCCCCACC 1970
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