| Tag | Content |
|---|
EnhancerAtlas ID | HS179-07724 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr11:122534080-122535160 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-5 | MA0063.2 | chr11:122534698-122534708 | CTCAAGTGGT | - | 6.02 | | OLIG2 | MA0678.1 | chr11:122534986-122534996 | ACCATATGGT | + | 6.02 | | OLIG2 | MA0678.1 | chr11:122534986-122534996 | ACCATATGGT | - | 6.02 | | RUNX1 | MA0002.2 | chr11:122534729-122534740 | CTCTGTGGTTT | + | 6.14 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_25355 | chr11:122533849-122535327 | DND41 | | SE_31058 | chr11:122534201-122535253 | Fetal_Thymus | | SE_53452 | chr11:122534071-122535174 | Spleen | | SE_59613 | chr11:122525607-122628654 | Ly4 |
|
| | 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 |
| GH11I122663 | chr11 | 122534199 | 122535117 |
|
Enhancer Sequence | TGATAATTTA ATGAGGAAAC TGAGGTTTGG AAGATTAAGT ACTACAGAGA TTGAAGAGTA 60
TCCTGCCTCA CTGTTCTATC CTGTGGCTTT GATCACCACC TGCTCCCCAC CCTCAGCTGC 120
CTCAAAGTCC AGCTCCCTTT CAGGGAGTGG ACAGTCATTC GCAGAGCTAA AGGCGTTGCT 180
TTTCAGAGAG GCAGCCAACC TAGGGAATCC TGTGTCTCCC GCCAGCTTTG CTCCAGCTGA 240
TGATGATGTG GTGGTACTAT CACTGCCTCC CCAATCCCAG CCGGCATAAG CCTGTGTAAG 300
GGTATCTCCT TTCTTGGCCA TCCAGAAGCT GAAGAGACCC CATCATTATC TGCCCCATCC 360
ATCCTGCCCT GATAGACAGA AGTCTGAACT TGTGGCAGCC TGGCTTTGAA TTCCAGCTCT 420
GCCTCTTACC AGCTGAGGGA CTGACCTTGG GCAAGTTGCT GAACATGCTA AGCCTCAATT 480
TTCCTGTCTG TACAATGCAG ACAATAACAG CACTTGTCTT GAAGGACCTT TGTGAGAGAA 540
GGGTGCCAAA CCACGCAAAC AGCTGGAGAG CGCCTGGCAT TGGGCACACC CTCAGAAATG 600
AGGTCGGTAT TAGTGCTACT CAAGTGGTGA TGTTACTCCA CATGGCTCCC TCTGTGGTTT 660
GGTTCCTTGG TCGCCTTCCA CTTTTATGGT TCTCTGTTCC TCACTGAGCT TTGGGTATAA 720
GGCTGTAAGA TAGGGCAGAG GCCAGTGGAT GCTTTCTCCC TGATAACTGC ATTCTGCTCT 780
CTGTGCTTCT CTCTCTAGAG TGCCCAGAGG GGTGCGGGGC CTGAGAAAAA GCAGACCCAG 840
GGCAGAGAGA GCACCACCCA AGCTGCTGAC TATAATAAAT GGCAGGGGCT GGGGACTGGA 900
AGGGGTACCA TATGGTTGTC TTCTGATTAC TTTCAAATGG AATCAGACTC AAGCCTAAGA 960
GAGAGAGTGG GGAGAAAAAA CCACACTCAA GAATGGATCC TCTCTGCAGG GTGACAGACT 1020
CAGCCAAGCA GAATGCAGAG CCATTGCCAG AAGAATGAGA TGACTATGAT CCTCATTGAA 1080
|
