| Tag | Content |
|---|
EnhancerAtlas ID | HS047-29051 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr6:42514850-42516140 |
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: 2 | Chromosome | Start | End |
| chr6 | 42514887 | 42515402 | | chr6 | 42515662 | 42516014 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I042547 | chr6 | 42514739 | 42516325 |
|
Enhancer Sequence | AACAACTGTG CTTGAAGCTC TGTCTTCCCT TGATTTTTTT GACTGAAAGG GATGTGCCAT 60
CAATCATGAG AAAATTCAGG CGCCCTCCAA GATGCAGTTT GGCTCTGCCT CTGCCCGCTA 120
GAGGAATTCA CCCTGGACCA GATAGAGGCT TTTGTTTTTC AAGCCCCCTA CCACTAAAAA 180
GCAGGCATAG ATATTAATGG GCATCTTGGA TCCACATCTG GGTATTAGAT TATTAGAAGG 240
GCATCAGAAT TTGCATGCGG TCCGAACCAG CCACTGCCTC CGAAGCCTTG CAGACCACAG 300
TGCCTGCTGC CCTTCCTCTG GGTCCATATC ACCAATCAGA ATATGAAGTG TGTCTCCTTA 360
ACTGCTGATG ACCGGAGCCT TCTGGGAATT CCTGAGGGAG GGGAAGGACT TAGCCTGTGG 420
CTTCTAGTCC TGAGGATGCT CCCTTTGAAT GTCAGTTACC AGCTGCTTAT GGAAGCTAAG 480
ACAAGGGACA TCAAGTACTT CGGGGTCCCA AGCTGTATAA CAGGAATCGG TCACGTTCAA 540
ACAAAAGCTA GCTCCAGTGC TGAAGAGGAA CTCCAGAGAT CGAAAAGCTC AGCCCCACGG 600
AGGTTGGTCC CTCCTCCGGC ACTGCGGAGG CCAGCCTGGG CAAGGGCGCC CCCTGCAGGC 660
TCCCGGCATC GGTGCCGGAG AAGCACGGTG GACTCTGAGC TGCCGCCGGT TTTGTGGGTG 720
GCTTTGCCTC CCTCACTTCT AAAACCTCCA GCGGTGGCGG TCCCCTTATA CCCTGCCTGG 780
GGGGGATACT TGGAGAGGAG AATGAGGGGC TTCTTCCCAG TGGGCAGAAC CAAAGGCAGT 840
ACCGATGACT TGAAGCTGGG CTCTAGAGAG CAAACAAGAC TTTCCTGTAT TCAAATTCGC 900
AGGCAGTGAT TTATGTTTAG GCCACTGGCT TGGCTGCCGG CTGTGGATTC CATTGACTGG 960
CGGACAAAAT TAAGCTCCTG GTTCCTCACG TGGATGCCAT CAGATCCCTA GTGAAGAATC 1020
CCGTGGAACA AAGCTGTAGA TGTTCTGATA AGATGAGAGA GGCAGACAAG TGGTCACATG 1080
ACCAGAGAGA CCGTGGAGGA GTGGATGCTG CCTTGGCCTG GGGGAGGACC CAACGTATTT 1140
AGCAGTCCAC GCACGTGCTA CTCACAGCAG CCCTGTGAGC TTATCCTTTC CCTACCCTTT 1200
TCTGTGCCTG GAGGCACCGG CCTAAAGGTA GGTTATATTT CACTGCTGCC CTCTCATCAG 1260
AGCCAAAACT ATGTTGTCAC AATTAATGCT 1290
|
