| Tag | Content |
|---|
EnhancerAtlas ID | HS129-01214 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:59892540-59893710 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:59892939-59892957 | CCTTGCTGCCTCCCTCCC | - | 6.39 | | STAT1 | MA0137.3 | chr1:59893420-59893431 | TTTCCTGGAAA | - | 6.62 | | Stat4 | MA0518.1 | chr1:59893417-59893431 | TCATTTCCTGGAAA | - | 7.73 | | ZNF143 | MA0088.2 | chr1:59892977-59892993 | CAGTGCATGCTGGGAA | - | 6.53 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_51313 | chr1:59890494-59896195 | Skeletal_Muscle | | SE_52298 | chr1:59891466-59894046 | Skeletal_Muscle_Myoblast | | SE_64091 | chr1:59891451-59894110 | HSMM |
|
| | 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 |
| GH01I059425 | chr1 | 59891250 | 59894729 |
|
Enhancer Sequence | AAAAACTGGT TGCCTGCAAT TCTGTCAGCC AGTCCAGGCA ATGCTAATAC AGCTTTGATT 60
ATTATGATCA TGATTATTAT TTTGTTTTGA AACCTTTTTC AGAGGCCAAG CATGCTGGGG 120
ACTTGAGGGA CATAAAAATC TTTCAACTGA TTATGCCACC TGCAAACAGG ATAAGCCTGA 180
CTTTCTACCT CACCCACCTC TTGCTATCAC AGATATGAAT CAACGAACAC ACAAAAAAGG 240
TTTTCAATTC TCCCTTTGGA AAGAGGGCAC ATTTAATATT CTGAGTCAGG CAAGGAAAGA 300
CTCTAGCCAC AAAGACAGCT GGGAACTCAG GTCCATAGCA GGCACCCAGG ACGGAGGTGA 360
AGAGAAGGCG CCTCCCTGTC TGGTGACAGC AGCTGGGGCC CTTGCTGCCT CCCTCCCCAC 420
AAAAATCCAG TTGGGACCAG TGCATGCTGG GAATCTGCCT GCCTGACAGA AACAGATGGC 480
CTCAGGTGGT GACTGATCTC TTGGTGACAC TAACTGCATA GCTGCTGCTT TACTCATGAC 540
CGAATGAGAC ACGAGATGGC GGAGGTAAGA GTTGGTTACC TTGCCGTCTC CTCCTCAGCT 600
GAAATGACTC ACATTGCTGT AGCTTAAATT TCAGTCCAGG CTCTCTGGAC TCGGGGAATT 660
TCTTTTTGCT CATGCTCCTG AGAACCAGAG TTCTCCAGGA ACATCTGTAG TCTCTGTCTT 720
CAATCAAAGC ATTTGAGAGA TGCTTTATTT TTCCCCTTTC CTCTGTACCT GTCACAGAAG 780
GGGGCCTGTC TGAATAAGAT GGCACATAAT CTGCTGAGTG CAGCAACCCC TCTGTGCAGC 840
CTTGAGGAAG AAGACAAGGC AGTCAAAGTA CCTTCCATCA TTTCCTGGAA AATGTGTCGG 900
TAGCTTGGAG AGGCAGAGTG GGAGATGGAA GTAACACTGC ATGAGGAGTT AGGTGGTCTA 960
TGTTCAGGGG CCAGGGTTGT CACTTACTAG ATAGGGGACC TTTAGCCAGT CACTTAACTC 1020
CAATGGCCTT CTGCTTCATA TCATCTCTTA TGTAGGGTGG TGGGACTGGA TTAAGGACAG 1080
CAGATAGATT AGCTGTCAGT CTTACTGATT GGAAGTTGCT GTCCAGAGTA CAGTATGGGG 1140
GATGGCTGGG AAGCCCATCT CAGCTAAGTG 1170
|
