| Tag | Content |
|---|
EnhancerAtlas ID | HS061-15213 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr2:242471380-242473760 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr2:242471796-242471811 | TGGCCTTTGGACCCG | - | 6.48 | | IRF1 | MA0050.2 | chr2:242473117-242473138 | TTTTTCTTTCTTTTTTTTTTT | + | 6.59 | | ZNF263 | MA0528.1 | chr2:242472072-242472093 | TGGGGAGGGGCTGGAGGAGGG | + | 6.14 | | Zfx | MA0146.2 | chr2:242473376-242473390 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGCCTCCCGA GTAGCTGGGA TTACAGGCAT GCACCATCAT ACTCGCTAAT TTTTATATTT 60
TTAGTAGAGA TGGGGTCTCA CCATGTTGGC CAGGCTGATC TCAAACTCCT GACCTCAAAT 120
GATGCGCCCT CCTCAGCCTT CCAAAATGCT GGGATTACAG GCGTGAGCCA CCATGCCCGG 180
CCCTGTATGT TAATTTTTAA ATGAAAGCTT TTAAATTAAT AATTCCTAAA TGTCATCCCA 240
TATGGAGTCA GTGTCCAGAT TTCCTATCTG TACATAGGAT TTCCCAAGAG CAACTGCATA 300
CCATTGGTTC ACACTTCCAT CCCTCCACAC CTGTTTCCTT GTCTCTTAAC TCTCTTTTTG 360
CCCCTGCAAC GGAGCAGCGG AGGATATCGA GCCTCCAGTC TGTGGAGGCC ACAAACTGGC 420
CTTTGGACCC GGTGCCACCT CCCTGTTCCT CAGCGCCCTT CTCCTGCGCT TGGCAGTAGG 480
TGGCAAGGCT CGTGGGCTTC TTGGCTTCTG TGGGAAGCCC ACCTCCTCTC CCGCAAGCCC 540
AGGTGGTCTT TATCAGACTG CACACTCCCT CAAGTTGGGG TACAGTGGTG TGATGGTGGC 600
ACATCTTCCT GGAAAGTCCC ATACCCCAGG GTGTCTAAGG ACACCCCACC AGGCCCCCAG 660
CCCCGTCTCC TGCAGAAGCT GCAGCTTGGC CTTGGGGAGG GGCTGGAGGA GGGCAAAGCC 720
CCCAGGATGG GTGAGCACCA CCCTCCAACC AGGGGCCACG GAAACGGAGG GAAGAGGAGA 780
TGTGGAGACA ACAAGCAGGG CTGCCTCGCC CGGGGGAGCT GAGGGCCCAG AGCCAGCTGA 840
CCCACCACGC CAAAGCAAGT TCAGCCTCAG TCCCACCGGA GTGCCACGAC TGGGCAAGCC 900
ACCCCTCCAG TACAAACCCC CAAGTCAGAG GGGCACGGCC GCAGGGTGGC AGCAGCTCTG 960
TCACTGCCCT GGGCTGCACA TTTGGCTGTA GGCCTCACGG ATGAGGACCT TGCCCTTTTG 1020
CAGACCTCCA GGTGTGACTC CAGCCAGGGC CCCGTGACGG AGCCTCCAAT GGGTCCCACC 1080
GGTCCGTCCG CTCAGCAGCT GCTTCTGGAA GGCCATCATC AGCTCCGCCG GTCCGTCCGT 1140
TCGGCAGCTG CTTCTGGAAG GCCACCATCA GCTCCCCAGC CCCTTCACTC ACTGTCCCTT 1200
GAGGGGTTCC AGGAGGCCAT GGCTGAGAGG TGCTGCAGCC AGGAGTGCAG ACCCCATCGC 1260
AGGGAGGACA GATCACTCCC CCACGACACA AGGAAGGCCA CCCCGAGGTG TGGGGGCAGG 1320
CCTGGGGGTC TCACTTCTGG GACTACGACC ATGCTCTTCC TCCAGGTCGC CCACCTTCCT 1380
CCTTAGCACA GGGCCCCAGG TCACAGAATG ACTCAGGCCT GGGAGCTGGG TGAGGGCGAG 1440
GACTTCCCCA GGGCTGCTCC AGACCTGGGT TTTCTCAGCC CACTGCCCTC ACCAATTGTT 1500
AACCTTAGTG GCTGCCCTTT GTGTGGTCCA GCGGATCCCA CAACCACCGG AAGGCACCAG 1560
GGATCTCTGC AGGCCCCCCC CCAGCCCCTG CCACCTCTCC CTCTTGCTGC CAGTCAGGGA 1620
GTAGCTACTC AATGCACCTG CTTCATCAAG GTATCCATGC CAGCTGCAGG GTGCCCCTGT 1680
GCACCTTCTG TCCTTAAGAG CTGGCCCAGG GTGGCATCCC CCCACCAGAG TAAGTCTTTT 1740
TTCTTTCTTT TTTTTTTTTT TTAGACGGAG TCTTGCACTG TCGCCCAGGC TGGAGTCAGC 1800
TGGAGTCAGC TGGTGTGGTC TCAGCTCACT GCAAGCTCCG ACTCCTGGGT TCAAGCGATT 1860
CTCCTGCCTC AGCCTGCCAA GCAGCTGGGA CTACAGGCAC CCGCCACCAC ACCCGGCTAA 1920
TTTTTTGTAT TTTCAGTACA GACGGGGTTT CCCCGTGTTA GCCAGGATGG TCTCGATCTC 1980
CTGACCTCGT GATCCGCCCG CCTCGGCCTC CCAAAGTGCT GGGTGGCATG AGCCACCACG 2040
CCCAGCCCCA CCAGAGTATT TCTAAGCCCC TTGGGAAGGG AGGGTCTTTG GGTCCCTCTG 2100
GGGGCCTAGG TAGAGTAGGG TGCAGTGTTA TCTGCTATAA TATGCTTGTC TCTCTCAGTC 2160
TTTGCATTCC TTTTCTGCAT CATGCCATAT GGCATTTTAG CCATTTTGAC CTCATTTAGA 2220
ATGTGCCACC TTTGGATCCA GGTGCCAGCA GCAACGGGGC AGATGATGGG AATCCCTCCC 2280
CAGCACCCGG CCAAGAGTCC CGGCCCACCC AATGTCAACT TCTATTCTTT AATCTCAGCC 2340
CCAAATGACT GTGAATTCAC AGGGCATTCT TCTAGCTCCA 2380
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