| Tag | Content |
|---|
EnhancerAtlas ID | HS069-01315 |
Organism | Homo sapiens |
Tissue/cell | GM18951 |
Coordinate | chr10:119255670-119257030 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr10:119256214-119256233 | TTTCCAGCAGGTGGCAGCC | + | 6.76 | | MSC | MA0665.1 | chr10:119256447-119256457 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr10:119256447-119256457 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr10:119256447-119256457 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr10:119256447-119256457 | AACAGCTGTT | - | 6.02 | | Twist2 | MA0633.1 | chr10:119255979-119255989 | AACATATGGT | - | 6.02 |
|
| | 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 |
| GH10I117496 | chr10 | 119256141 | 119256390 |
|
Enhancer Sequence | CCTCTTTCTG ATCAGTACCA TGACCTTTCC TCGTGGCCCT CTCCCCCCAG CACCGCAGGC 60
CTCCTTGGTA TTCTCTGAAT GACATGAGCG CATTCCTACC CCAGGGCCTT TGCACTCCCA 120
GCCAGCCTCA CTCTTCCTCC ATGGAAATTT CCCTCATTTC CTTCAAGCTT TTGTTCAAAA 180
AGCTTCAGCC TTCTCAATGA GGCTGACCCT GAAAACTCTT TACAACTCAC CTTTCCCCAT 240
CGAGCACTTC AACCCCCCCT TACATGTTCT ACTAAAAAAA AAAAACTTCC CACATATTGG 300
TCACTTCCTA ACATATGGTA TCATGTATTT GTGATATTGT CTATTGCCTG TCACCCTCTG 360
AAAAATGATA AGCTCCAGAA AATCAGGTAT ACGGGTCTCT GTTTTGTTCA CTAAATCATT 420
CCAAGTGCCT AGGACTCTGG CTGACACATA TTTCCTGCTC CAGAAATATC TCTTGGCTGA 480
GTGAATGAAC CTCTTCCCCC AGCGAGCGAG CCTGTCGGCC GAGGAGACCA CGCCATACCA 540
GGATTTTCCA GCAGGTGGCA GCCGACGCAC GCCAGAGACA GCTGGGCGCC TACACTTTGA 600
ACTCAAGGTT CTTCCAATTA AGTGCAAGAT AAGGAGCTTG GAGACTCATC GCGTTTGGCT 660
TACTCCTGAC GCAGACTTGC ACTGGAGGTT GTGTGGAGGG GATGAGCCGG TGAGCTGATA 720
AAGCCTTTAT CTAATACGGG AGACTGTTTA CCCACAATTC AGGGGTAAAA AAATGTAAAC 780
AGCTGTTGAG AAGAAAGGTC AGAGTCCTCC CACGGTGGGG AAAAGGGGCA GAAGAAAGCC 840
TGTGGCCACG GATTGGCGTC ACTCCTGCAG ATGGAAAAGT GACATTGGAC AACTACTCAG 900
GGAAAAAGGT GAGCCCCTAA CACACCGCTG GGGTCGTGGA CGTTTCTAGT CTTACTTTTT 960
TTTTTTTTGA GACTTTTTTG AGTTTTGCTC TTGCTGCCCA GGCTGGAGTG CAGTGGTCTG 1020
ATGTTGGCTC ACTGCAACCT CTGCCTCCCG GGTTCAAGCG ATTCTCCTGC CTCAGCCTCC 1080
TGAGTAGCTG GGATTATAGG CGCCTGCCAC CACACTCAGC TAATTTTTTG TATTTTTAGT 1140
AGAGAGGGGG TTTCACCATG TTGGCCAGGC TGGTCTTGAA CTGCTGACCT CAGGTGATCC 1200
ACCCGCCTTG GCCTCCCAAA GTGTTGGGAT TACAGGCGTG AGCCACCACG CCCGGCCTAG 1260
TCTTACTCTT GACACACCAG AAGATGCTTT GTTATGAAAC CTTGAATCTT CCTGTGGGCT 1320
CCTGCCAAGC TGCCCTCCTC CCGGGTGCTT CTGTTATCCA 1360
|
