| Tag | Content |
|---|
EnhancerAtlas ID | HS002-08119 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr5:178068900-178070100 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GSC | MA0648.1 | chr5:178069575-178069585 | GCTAATCCCC | + | 6.02 | | Stat6 | MA0520.1 | chr5:178069835-178069850 | TTTTTCCTGAGAACT | + | 7.26 | | TFAP2C | MA0524.2 | chr5:178069693-178069705 | TGCCCCAGGGCA | - | 6.44 | | TFAP2C | MA0524.2 | chr5:178069693-178069705 | TGCCCCAGGGCA | + | 7.22 |
|
| | 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 |
| GH05I178641 | chr5 | 178068881 | 178070273 |
|
Enhancer Sequence | AGATTTTATA GCCCAAGGGA CAGGGCTGTG TACACCAAAG CTGAGACCTG CTCCGTAGTC 60
ATTTCCCGCT CTGGGTCTCA ATCCCGAGTA GCTTCTCCTA TGGTCATGGC TGGCCTCAGA 120
GGACGGCCCC CACTGAGCTT CTCGGTTATG CTGGTGACCT TCTCATCGGC ACTTTCCTTA 180
TCTCCTTGAA GGATGGAGCC TCTTCGAGGC CCTCTCACAA GGCAGAGTCA GCTGATGAGT 240
AGAGCACACC CTCTAGCATA TCTCCTTCTG GGTCTTATGT TCCCCTCATC TGCCATTTTC 300
CACAGCATTT GCAGCATTTG CACTTCCTGC AGGGTGACAG GCACTTTCCC CAGGCTTCAT 360
CTGTAGCAGC ACGTTAGCTT TGTCTCCCAG GGGCCTTGCC TCGGTGTTAG ATCCTGTGTC 420
ACAGCAGAGG GCTCCCGTAT CAATAAACTC GCCCTCCCAG GCTTCTGTTG CACAGCTCTC 480
AATGAGCACC TTTGGGATCC AGCCCATGTT TCCTCTTTCA GCTCCTGCCA GTGCTGTGAA 540
GCAAGTTCAC TGTGCTCTAG TTACCACACT GTCTGAATCT GGTAAGACAG AACACCCACA 600
TATAAATTAC ATGAAGAGGG TTTGTTACTT ACTCATAGGA AGCAAGGGAC AACGGAAGCC 660
CAGGATTCAT TGGAAGCTAA TCCCCAGGGC TCAGGAAAGC CCCCTGAGGT TGGATTGGAG 720
TCTTGCTGTG GTGTGTATGC TCCACTTGGA CTGCAGCCAA AGGGCCATGG AAGAAAGTGC 780
AACCTGGGTT TTATGCCCCA GGGCAACATG ACTCACTGGA ATAAGGCATT GAAGGACATC 840
CTGTTTCTGG GGTAGGGGGG ACTGGAACAG AGCCCAGGCC TTTCCAGCCA GCTTCTCCTT 900
ATCTCACATT GTTGTGTTCC CAGCACATTC TATGGTTTTT CCTGAGAACT GCAAGTAAGA 960
AAGAGGAGAG AACTGGGTTG GTCCAAGGCC ATCTGCAGAA CTGTCCTGCA AGTACTTGTT 1020
GGCAAGGTCC TGCAGTTCCT TTGCCTACGG TTCTTTCCTT CCCTTAAGAG GCCCAGCACT 1080
TGCCTGGCCA GATTATGTTG TAGCTTGACC CTAGTTACTG GTCTTGGGAC TGGGGAAGAG 1140
GGGATTGATC CTGAGAAGGG TGCATGCTTT CCTTTAAAGC AGAAGCCTCC AGATCTTCTT 1200
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