| Tag | Content |
|---|
EnhancerAtlas ID | HS129-31760 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr6:52976790-52978100 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr6:52977628-52977649 | ACCATGACCCAGGACAGCGCC | + | 6.33 | | ZNF263 | MA0528.1 | chr6:52977315-52977336 | CCTTCCCCACCCTCCAGCTCC | - | 6.07 | | ZNF263 | MA0528.1 | chr6:52977318-52977339 | TCCCCACCCTCCAGCTCCTCC | - | 6.41 |
|
| | 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 |
| GH06I053111 | chr6 | 52976675 | 52978470 |
|
Enhancer Sequence | TCTCTGGCAA GGGTGATGAA CTCAAACACC TGTGAAGGTC CAGAGGACAC CACAAGTGAG 60
TGAGGTGGAC CAGGTGTGCA GGCAGTGGCA AGCCAGACCC TGTGTCTCTT GCCTGAAAGG 120
GAAGCGGCTA CTCAGCTTCC GTTCGAAGAT TCTCTATAAG GCCTGACCTT CCTATTTTTA 180
AAGAGAAGCT GGAAATCCAT GTTGTTTGTG AAATGTTGTA TGCTTAACCA AACTCAAGTT 240
TAAAAGGAAA AAAATAAAAA CACGATACAG GTCAAACAAA AGCCATCTGC AGGATGAGTG 300
GAATCGGCCA ATTTTTGACC CTTGGTATGC AGGTTAAAGC CCAAATAATA AACTTTGCAT 360
TCTAGGTCTG TACAGGTTTG ACACTAACCT ACCTTTCCAG CTCGCCTCCT GCTCCTCCTC 420
CAGGTCTGCT CCTAGCCAAG AATAGTTCTG GTTCCCAGGA CACCCAAAGC CCCTCCCTAC 480
CCCTGCCCCT TTGCTCTGCT GGCATCTGGA ATGCTCTTTC TCTCACCTTC CCCACCCTCC 540
AGCTCCTCCT GGAAGTTCTA CTATTCCTCC TGGAGGCTTT CCACAGTTTA ACTCCAGCCA 600
ATGAATGATT AAATAATTAC ACACAATCTA CTCCCCCTGG GCCTCCAGGG CACTCTCAAA 660
GAGCTCTGTT TCACCTGTGT TTACTTTCTA CCACATCCTG GCCAGTGCCA CACCTCAGAA 720
GGCTTCAGAG AAAAATTGTG ACTAACTGAC TTGTGTCACT TCTCTCCTAC TAAATCATAA 780
GCAAGTTGTC TGCAGAGCCC CCCACTGCCA GCTCCTTGCC CCAGCTCCTC CCACCACCAC 840
CATGACCCAG GACAGCGCCT TATAGGTCCC AGATGACTGT CAAGGCTTCT TGAAAGCTTT 900
GGCTCTAAGG GATTAAACTG GAAGACTGCA GCTGATTAAC TCACTAGGTT TAAATTAAGT 960
TCTTGGGCTT GCTGCAAGCA GAGCAAAACT CTCCCGTCTC TCTGCAGCCC CTTCTCAGGC 1020
CTCTGCTCTC TTTGTGGGCA TGGCCAGTGT CTCTTAGCTG CATCCTGGGT CACTCAAGGT 1080
CTCAGGGTAG GAGAGCTGGA TGTACAAATC ACACCCTCAT CCTCCTGGGG GAGTGGATCC 1140
AGGTGCTGGT GGAGGGATGC CAGCATCACC TGGAAGCAGA AAGTTATGCC CTGAGGGAGC 1200
TGTCCCTTGT TTGACTAATC CAAATTAATA CCACTATTAT TGTCTTACAG TGTTAGGGCC 1260
ATGAGAGGCC ATATAGCCAT TTAGACTGAA GGAGGAAACC GAGACCCAGA 1310
|
