| Tag | Content |
|---|
EnhancerAtlas ID | HS184-26296 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr6:42514990-42516140 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr6:42515493-42515512 | GGGCGCCCCCTGCAGGCTC | - | 6 | | MITF | MA0620.2 | chr6:42515918-42515936 | AGTGGTCACATGACCAGA | + | 6.38 | | MITF | MA0620.2 | chr6:42515918-42515936 | AGTGGTCACATGACCAGA | - | 6.38 |
|
| | 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 |
| GH06I042547 | chr6 | 42514739 | 42516325 |
|
Enhancer Sequence | GATAGAGGCT TTTGTTTTTC AAGCCCCCTA CCACTAAAAA GCAGGCATAG ATATTAATGG 60
GCATCTTGGA TCCACATCTG GGTATTAGAT TATTAGAAGG GCATCAGAAT TTGCATGCGG 120
TCCGAACCAG CCACTGCCTC CGAAGCCTTG CAGACCACAG TGCCTGCTGC CCTTCCTCTG 180
GGTCCATATC ACCAATCAGA ATATGAAGTG TGTCTCCTTA ACTGCTGATG ACCGGAGCCT 240
TCTGGGAATT CCTGAGGGAG GGGAAGGACT TAGCCTGTGG CTTCTAGTCC TGAGGATGCT 300
CCCTTTGAAT GTCAGTTACC AGCTGCTTAT GGAAGCTAAG ACAAGGGACA TCAAGTACTT 360
CGGGGTCCCA AGCTGTATAA CAGGAATCGG TCACGTTCAA ACAAAAGCTA GCTCCAGTGC 420
TGAAGAGGAA CTCCAGAGAT CGAAAAGCTC AGCCCCACGG AGGTTGGTCC CTCCTCCGGC 480
ACTGCGGAGG CCAGCCTGGG CAAGGGCGCC CCCTGCAGGC TCCCGGCATC GGTGCCGGAG 540
AAGCACGGTG GACTCTGAGC TGCCGCCGGT TTTGTGGGTG GCTTTGCCTC CCTCACTTCT 600
AAAACCTCCA GCGGTGGCGG TCCCCTTATA CCCTGCCTGG GGGGGATACT TGGAGAGGAG 660
AATGAGGGGC TTCTTCCCAG TGGGCAGAAC CAAAGGCAGT ACCGATGACT TGAAGCTGGG 720
CTCTAGAGAG CAAACAAGAC TTTCCTGTAT TCAAATTCGC AGGCAGTGAT TTATGTTTAG 780
GCCACTGGCT TGGCTGCCGG CTGTGGATTC CATTGACTGG CGGACAAAAT TAAGCTCCTG 840
GTTCCTCACG TGGATGCCAT CAGATCCCTA GTGAAGAATC CCGTGGAACA AAGCTGTAGA 900
TGTTCTGATA AGATGAGAGA GGCAGACAAG TGGTCACATG ACCAGAGAGA CCGTGGAGGA 960
GTGGATGCTG CCTTGGCCTG GGGGAGGACC CAACGTATTT AGCAGTCCAC GCACGTGCTA 1020
CTCACAGCAG CCCTGTGAGC TTATCCTTTC CCTACCCTTT TCTGTGCCTG GAGGCACCGG 1080
CCTAAAGGTA GGTTATATTT CACTGCTGCC CTCTCATCAG AGCCAAAACT ATGTTGTCAC 1140
AATTAATGCT 1150
|
