| Tag | Content |
|---|
EnhancerAtlas ID | HS130-02541 | Organism | Homo sapiens | Tissue/cell | MDA-MB-231 | Coordinate | chr1:204560260-204561730 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:204561216-204561234 | GGAATGAATGAAGCAAAG | + | 6.24 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 204560899 | 204561181 | | chr1 | 204561583 | 204561691 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I204591 | chr1 | 204560516 | 204561648 |
| Enhancer Sequence | TGGTAGAAAT TAAAACAGTG GTGGTCTCTG GTGGAAATTT TCTAGGGTGA TGGAAGTATT 60
CCATACCTTG ATTTAGATGT TGGTTATATG GGTGTATACA TTTGTCTAAA CGTGTTGAAT 120
GGTACACTTA AAATCTGTGC ATCTTACTGA ACATAAATTA TAATTATATC TCAAACAAAC 180
GAACAAAACA ACTTTTTCTC TGTCCTTGGG AAGAAGAGAT TTTCCCACTC TTCTTCATTG 240
TAAAGAGGTA GATGGCTGGG GCCCCCAGGA AGCAGTTAAA TGTGGTAGAA AACACATTGG 300
CTTTGGAGTC AGGCTCTGAT TCTGATTCTA TTTTGCCATT TGTGGCCTTG GACAAGCTGA 360
TCTCCAATTT TCTAATCTTT AAAATGGGCT GGGAGAGTGT TGTGATGATG AAATGAACTA 420
ATACAGTAAA GTGCCTGGCA TATAGCTGGT GCCCAAGCAG CTCCTTCTGC AGGAAGCCTT 480
CCCTGACTTC TCCAGACCTG GTCAGGTACC TTCATTTCCA CACACCAGCC TTGATGCATG 540
TGTCATTCAA AGCCGTGTGT CAACAACAGT GCAGATCTTT GACAGTCACA GACCTTTGTG 600
GGTATTTACT GAATAGTCAA ACGGCAAATA TGGAATCTGC AAATGCCAAG AGCCTACTAT 660
ATTGGAACAT TTTTATCTTT CTGGTCCCTA CTCTCTCCTA GGCTTTCAGA TCTTGAGGGT 720
ACAACGTGGT TATTTCTCAG CTTTGCTTCT CCCCAGCTGT CAAAAGTGCT CAATAAATAT 780
TTGACCACTG AGTAACTTTT AAGTTACTCA TGCATGAGTA ATTGAATAAA TGCATGAAAG 840
AATGCATACA CTAGTGAATG TATGAATAAT AGAATGAGAC AATTAGTGCA TAAGTGGGGG 900
AAATAGGTGA ATGGTGAATC AAGAAATGAG TAGAGAATTA AAGGAGTGAA GGTGAAGGAA 960
TGAATGAAGC AAAGCTGGTT ACCTTTCTTC CAAAGGGCTA TGTGCTGGTG ACAATACAAA 1020
TGGGCCCATT CCAGAGCCCT GGAGAGAGTT AGAGCTGGTC CACCTGACAG ACAGCCACGA 1080
GTGACAGCCC AGCCACTGGG GTCCTCCAAA TGTACTCATT CTGGAAACTT CTCCTTTCCT 1140
TCCAGCCACT ATCTGCCACC CCTCCATGGA GCTAGGGACG CCAAGGGACT GTGAGGCAGG 1200
GCATGACTCC AGGGGGCAGA GAGCTAAGTG CATGGCTGTC CTCTCTCTTC CCAAACCCTT 1260
GTCACAGGCC GTGAGGGCCT GCTGCCTCCC CTGATGCCAT GTTCCTGAGC AGATGTTCCT 1320
CCTGTCTTGT CAGCAACAGA GCGGCTGTCA GGAGTCCGCA TTATATATCT GCTCGGTAAC 1380
GTTTACTGGG ATTTAGTGTT TAACAACTGT CACTCCAATA TATCTTTTCT TAATCCCTTC 1440
AGATCTGCTG CTGTAGCAAC TTTAAATATT 1470
|
| |
|
|
|
