| Tag | Content |
|---|
EnhancerAtlas ID | HS129-24687 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr3:11253080-11254490 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYA | MA0060.3 | chr3:11253725-11253736 | AGCCAATCAGA | + | 6.32 | | Six3 | MA0631.1 | chr3:11253814-11253831 | AGATATGATATCCTTTT | - | 6.03 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_01696 | chr3:11252798-11254817 | Aorta | | SE_34785 | chr3:11252905-11255092 | HeLa | | SE_38057 | chr3:11252567-11255940 | HUVEC |
|
| | 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 |
| GH03I011211 | chr3 | 11252945 | 11254843 |
|
Enhancer Sequence | TAGGACCCTT TTGTTTCCAC CTGCTAAGGC AGTACCTACT GTCAACATGT AACTTCAACA 60
AATTAAGACG TGAAACAGTG TTTCATAATC ACAATTAGGC ATTTCTGTTA TACTTCATGA 120
TCAGAGGCTT AGGCAAGGTC TGACCCCCTC TCCAGCTGTG GCTTGTATCC AAGACCCAGG 180
GCAGCTCCAT GCCTCAGCAC CGGGGCCTTC CTGGCTATGA CCCAGAGAGC AAATGCTCGG 240
CAGAGTCCAG AAGCTCAAGT CAGGAAGATA AATGAAGAGA GTTGGAATGG ACAGGGGCAA 300
GGACTGGGAT TTCAAGATTC TCCACCACTC TGATTTGGCC AGGAGCATTC TGACCTCTGC 360
CAGGAGCTAA AATGTGCCTC CCTGTGGTCT GAGAAAGGAT TGGAGTCACT TCATCCTTTA 420
AGCATAGATG CAGAAGGCTA GGGCTACTGG GACTATTCCT GTGGTTTGGA GAAGCGTTTC 480
TTAGACAGGC TGTATCAGAA TCATTGGAGG TTCTCTATTT GAAGTGCAGT GTCCGGGCTT 540
CCTCCCAGAC CTCCTGAATC AGAGTTCCCA GAATCTGCAT TTTAACGTAC GCACTCCCAA 600
GTCAGAATAG CTGGTTAGTT GGCAGTGGGG CTGGGGGAGG GGGGCAGCCA ATCAGAAGAA 660
TATTTGCTAT TGGGATTGTC CTGGGAATGC CAGGGCACAC GCTTGCTGTC CTGCCGTGAA 720
ATGGCCACCT CCCCAGATAT GATATCCTTT TGCCTCATAG AATTGCGACA GGAATAAGGA 780
CAGGAATTTC AGAAGTTTGC AGAGTAGATT TTCCTGCTGT GAGGCAGTGT ATGTGAGAAG 840
GCTCTGCCTT CCTTCAAATG AGAAGGAAAA AGAAAAGAAA AAGCTTTATA TATATGTATA 900
TATATTTTGG AGGCAAATGT GTCACTTTCA GATGGGTTCT TTTCCAGTCT GGGCACAATT 960
TTCATTTCTC TCTGGTGAGT CATTGCAGAC GTTGGCTTTT TCTCACTGCC TCTTGTTAGC 1020
AAAGGACATA TTTCATGGAA GGGCTGAGAC CCATCTGGGG CAGGCCTGGA AAATCTACTC 1080
TGCAAATCCA GGTAGAGGAC CCACTGGGGC TATCACGGGG CCCTACACAG TCCTGTGCTG 1140
TGGGAGCCTC AGAGACTCCC GGCAACCAAG GCAATGGGCA CTTTTCCCCC TTCCTAATTA 1200
GCCCTCCTTG TTAACTCACA TCTTGCCCTT CCATGCGTTG TTTCTAGACT CTCTGGGCCA 1260
CCATCCTGCT GGTTTTAATG AGAAAAAGTC CACAAGTACC TTTCGGCATT CATTCACGTA 1320
ATCCATCAGT AGTATAGCAT AGCAATTAAG GACATGGGTT CTGGGAGTTG TCCTTTAGTG 1380
GCTCCCTGTT TCATCAAAGT CAAAACCGAA 1410
|
