| Tag | Content |
|---|
EnhancerAtlas ID | HS003-21909 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr18:56074140-56075780 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXC1 | MA0032.2 | chr18:56075064-56075075 | ATATTTACTTA | - | 6.14 | | Foxq1 | MA0040.1 | chr18:56074894-56074905 | TATTGTTTATA | + | 6.32 |
|
| | 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 |
| GH18I058406 | chr18 | 56074075 | 56076162 |
|
Enhancer Sequence | ACGCCAGTGG AATACGGGAT GCCAGCACAG TGGGAAAAGA CAGCCTGATC TCTGGGACAG 60
CCCCAGTTTC AGCACTTAAA AGACACTGCA CTGCCTTTCT GGCTGCCACA GGACAGAACC 120
CCCCGCCTCC CTCCAGCCTT TCCCACACCA CAAAACAAGC ATCTAATATT TTCCAGGGAC 180
CTTCCAGGGA CAACACAAAC TTCCCTTTGT CCAACAGAAT TGAAGGGTGA AGGGACCAGA 240
GACTGAGGAC TGGATTTTCT ACTCCCAGGA ACTCCTTGAT GGAGCTCTGA GATGCTGAAT 300
TTTTTAAAGA GTTTCTGTTA TTAAAGGATT TTAGATATTA AGTTGTAACA TACAGTCATG 360
CACCACATAG ACATCTCAGT CAGCAATGGA CTCCCATAGA CGATGGTGGA CCCGTGAGAT 420
GATAATGGAG CTGAAAAATT CCTGTTGCCT ACTCATGTTG CCTAGTGACA TCATAGCCTT 480
TGCAACCCAT CACCCTTTCT ATGTTTAGCT ACGCTTAGAT GCACAAACCC TTATCATTGT 540
GTTACAATTG CCTGAACAGA ACAGTCACAT GCTGTACAGG CTTGTAGCCT CGGAGCAATA 600
GGCTGGACCA TATAGCCTAG GTGTGTAGCA GGCTATGCCA TCCAGGTTTG TGTGAGTACA 660
CTCTGATGTT TGCACAACGA TGAAATCGCA TAACAACGCA TTTCTCAGAA TGTGTCCCAG 720
TTGTTAAGCA ACACATGAAC ATGACTGTAT TTAATATTGT TTATAGCAGA AAGTTAGAGT 780
TTGGGATTTG TCTTTTGAAT TCTAGTTATG TAGCTCTCTT AGCAATTCTA AGACTCTGCC 840
ACTAGGGTCA TCACCCTCCC TCACAACCCC TCTCACCATG ACCTCAACCC CCATCCTGGC 900
CCCCTCTTGC CTTCTCTGCA TTCTATATTT ACTTAGAAGA TCCTTGCTTG TTCATGAGTT 960
GAGATTGTCA GGGGGACATG CCCTCCGCAA TGTAATGAGT GTTTAAACAA CAGTCAGGCC 1020
TTTGAACCCC AGGCTCCAGT TAAAAAGTAA CAGGCTAGAT ACTGAATCAA TAGGAGGCAA 1080
ATATTAGCTA CGGAGGCTGA GAGAGACCGA GTTGGGAAAC ACTTGTTGCT GGTGACATGC 1140
AAAGAGCAAT GGCCATACCC ACCTGAGGTC CAGGAAGCCC TGGGAGCCCC ATGACCTTCG 1200
GCCTGTCATT GTCCTGCTCT ACATGTTGTA ACATTGAAGC CACCAGCCCT TAATTAGCTT 1260
CTAGACCTCC CTCAGTCTGG ACTTCTGCAA TATCCCACTA AATGGTGTCC ACCTGATTTT 1320
TCCCCTTCCC AGCCATCTTA CACTCATGTG AGCCTGCTTC CAGCAAACTC TGATCTTGTC 1380
AATCTTCTGC TGGAAAATTT TCCATGACTC CCCATTGCAT TCCTGACTGG TGCGCAAGGG 1440
CATCTACCTG CTCTTTGGGA CGTGGGCAGG GGGATGGCAG ATCTCCAGGT GGTCACATCT 1500
AACCACCAAT TCCCAGTCTT CTTTCTCCCC CGTAGTGTGC TGCCTTCAGT GTTATCGATG 1560
ATTTCTTCTG TCTTGATACT GTGTCTTTGG TTTCCATGAC ATTTCAATCT TCTGGTTACT 1620
CTCTCACTCT TCAAATACTC 1640
|
