| Tag | Content |
|---|
EnhancerAtlas ID | HS130-22043 |
Organism | Homo sapiens |
Tissue/cell | MDA-MB-231 |
Coordinate | chr5:178068760-178070090 |
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 | TCTGTGTCTT TCTGCATCGT CCCTCTGAGA CCTGAGACCT CTCAACCCAC AGAGTGTAGA 60
ATTGTGGGGA AACAAAGCAC AGACTCTCCT CGTGGTGTTT TTGCCACATC ACAGATATCT 120
CTAATACTGT AGGGTCTTCC AGATTTTATA GCCCAAGGGA CAGGGCTGTG TACACCAAAG 180
CTGAGACCTG CTCCGTAGTC ATTTCCCGCT CTGGGTCTCA ATCCCGAGTA GCTTCTCCTA 240
TGGTCATGGC TGGCCTCAGA GGACGGCCCC CACTGAGCTT CTCGGTTATG CTGGTGACCT 300
TCTCATCGGC ACTTTCCTTA TCTCCTTGAA GGATGGAGCC TCTTCGAGGC CCTCTCACAA 360
GGCAGAGTCA GCTGATGAGT AGAGCACACC CTCTAGCATA TCTCCTTCTG GGTCTTATGT 420
TCCCCTCATC TGCCATTTTC CACAGCATTT GCAGCATTTG CACTTCCTGC AGGGTGACAG 480
GCACTTTCCC CAGGCTTCAT CTGTAGCAGC ACGTTAGCTT TGTCTCCCAG GGGCCTTGCC 540
TCGGTGTTAG ATCCTGTGTC ACAGCAGAGG GCTCCCGTAT CAATAAACTC GCCCTCCCAG 600
GCTTCTGTTG CACAGCTCTC AATGAGCACC TTTGGGATCC AGCCCATGTT TCCTCTTTCA 660
GCTCCTGCCA GTGCTGTGAA GCAAGTTCAC TGTGCTCTAG TTACCACACT GTCTGAATCT 720
GGTAAGACAG AACACCCACA TATAAATTAC ATGAAGAGGG TTTGTTACTT ACTCATAGGA 780
AGCAAGGGAC AACGGAAGCC CAGGATTCAT TGGAAGCTAA TCCCCAGGGC TCAGGAAAGC 840
CCCCTGAGGT TGGATTGGAG TCTTGCTGTG GTGTGTATGC TCCACTTGGA CTGCAGCCAA 900
AGGGCCATGG AAGAAAGTGC AACCTGGGTT TTATGCCCCA GGGCAACATG ACTCACTGGA 960
ATAAGGCATT GAAGGACATC CTGTTTCTGG GGTAGGGGGG ACTGGAACAG AGCCCAGGCC 1020
TTTCCAGCCA GCTTCTCCTT ATCTCACATT GTTGTGTTCC CAGCACATTC TATGGTTTTT 1080
CCTGAGAACT GCAAGTAAGA AAGAGGAGAG AACTGGGTTG GTCCAAGGCC ATCTGCAGAA 1140
CTGTCCTGCA AGTACTTGTT GGCAAGGTCC TGCAGTTCCT TTGCCTACGG TTCTTTCCTT 1200
CCCTTAAGAG GCCCAGCACT TGCCTGGCCA GATTATGTTG TAGCTTGACC CTAGTTACTG 1260
GTCTTGGGAC TGGGGAAGAG GGGATTGATC CTGAGAAGGG TGCATGCTTT CCTTTAAAGC 1320
AGAAGCCTCC 1330
|
