| Tag | Content |
|---|
EnhancerAtlas ID | HS129-11865 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr14:71248490-71249820 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr14:71249642-71249660 | CCTTCCTTCCCTGCTACC | - | 6.77 | | EWSR1-FLI1 | MA0149.1 | chr14:71249638-71249656 | CTTTCCTTCCTTCCCTGC | - | 7.24 | | Foxa2 | MA0047.2 | chr14:71248901-71248913 | TGTTTACATAGC | + | 6.32 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_36405 | chr14:71247656-71254025 | HMEC |
|
| | 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 |
| GH14I070781 | chr14 | 71247857 | 71250079 |
|
Enhancer Sequence | AGCCAGGTCT GCCTGATTCA GAGCCCACAA CTGTACCAGC CCACAACTGT ACCAGCCCAG 60
GTTCTCTGGC CACTTAGAAA GAGGAGCTGT TTCACATGGA AGACTCAACT TCTTGGGAGC 120
ATGGCTTTCC TAGTCAACAT TCCAGGTCTG GGAATTGCCT AAAGAACCCA GGTGATGGGA 180
CATGGCATCA GTGAACACTT GGCTCTGTCT GAGCTGGGGC AGGCCGCCTT CCCTGGGAGG 240
TCATAGCTAT GGCCTACCTG CCCTATTACC AACTCTTGAA TCCTACCCCT TCTTTGAGGC 300
CTAATTGTTC CATCAAGGCC TCCCAGGGAA TTCTGCCTTC TCCAGACCCC ATCTCATGTA 360
TCTTGACACG CTGCCCCCTA CTACATCACA CTGTTCTGGT TGTTTAGGAT GTGTTTACAT 420
AGCACAACTC CTAAGGATGG AAAGAATGCA GTGGAAGTGA CCTCTATGTT ATGTATATAA 480
TAAATTGACC GTATTTCTTA CAGCATGTAT GCAATAGCAG GCACGTCAAT TTCTTATGAG 540
GACATTTGGG TAATAAAATT ACCCACATCG GTTGAGAATC ATGATCTATA CAAAAAGAAA 600
ACATTCCAGG CTCTGTGACC TGCACTTCAC CCCAGGCATT GCAGAGGAGA AAGGATTTGA 660
GGGCAGAGGA GGAAGCGGTA CAAGCCACCA CAGATACCAC CTTCATCCCA TCACCTTGCA 720
GGCAAGGAAG TCCCAACCAC AAAGGCTCGA AACACTGGGA GTTGCCATTG TGAACCACAA 780
GTCCTTAATA GCCCTGGAAA GCTATGAAAC ACCAATTAAA GTTTCCTATG AATCACTTTT 840
CAACCTCTCC ATGTAAGAGC AGGGAGGAAC CAACCTCAAG TACCTCCTCA GGCCAAGACT 900
AGCTTTGCTC TGACTCACTG TCTTTCAGTC TATGATATGG ATGCTTTTCT AATTCCTTCC 960
TCCCACCTCC ATGTCCATTG CATGGGGAAG ATGAGACTTC CTAGCATCTT CCTAGTCTAC 1020
CTCTGAATAT TACTCTACAA ATCCTGTTCC CCATGAGACA GAGTTGAGGA TCTCACCATG 1080
GTAGGGAAAA TTCAAAACTA TACAAATTCT CTAGATGTTA CACCTCAGTT TCCAGGTGAA 1140
AGCCAGTCCT TTCCTTCCTT CCCTGCTACC TGGAAGGTGG GCATAACAGG CATACCCAGA 1200
AACTGCTGGG AAAACGCTCA AATGCCGTGT TCTCTGCCTT CAGTGAATGC CCATGTAAGG 1260
AAAAGTCTTA GAATATCTTA TTTTTCCTCA GTGGGGTCAC TTTTACTCTT CCTGGAAGGT 1320
CATTATCCCA 1330
|
