| Tag | Content |
|---|
EnhancerAtlas ID | HS146-03152 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr11:122533990-122535160 |
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 | CAGAATTTCT AATAATACCT TAAGTTTTTA GACCATGTTC GAGCTTACAA AGCAGAGTCA 60
CATACATAAT CACTATTAAG TCTCAGACAT TGATAATTTA ATGAGGAAAC TGAGGTTTGG 120
AAGATTAAGT ACTACAGAGA TTGAAGAGTA TCCTGCCTCA CTGTTCTATC CTGTGGCTTT 180
GATCACCACC TGCTCCCCAC CCTCAGCTGC CTCAAAGTCC AGCTCCCTTT CAGGGAGTGG 240
ACAGTCATTC GCAGAGCTAA AGGCGTTGCT TTTCAGAGAG GCAGCCAACC TAGGGAATCC 300
TGTGTCTCCC GCCAGCTTTG CTCCAGCTGA TGATGATGTG GTGGTACTAT CACTGCCTCC 360
CCAATCCCAG CCGGCATAAG CCTGTGTAAG GGTATCTCCT TTCTTGGCCA TCCAGAAGCT 420
GAAGAGACCC CATCATTATC TGCCCCATCC ATCCTGCCCT GATAGACAGA AGTCTGAACT 480
TGTGGCAGCC TGGCTTTGAA TTCCAGCTCT GCCTCTTACC AGCTGAGGGA CTGACCTTGG 540
GCAAGTTGCT GAACATGCTA AGCCTCAATT TTCCTGTCTG TACAATGCAG ACAATAACAG 600
CACTTGTCTT GAAGGACCTT TGTGAGAGAA GGGTGCCAAA CCACGCAAAC AGCTGGAGAG 660
CGCCTGGCAT TGGGCACACC CTCAGAAATG AGGTCGGTAT TAGTGCTACT CAAGTGGTGA 720
TGTTACTCCA CATGGCTCCC TCTGTGGTTT GGTTCCTTGG TCGCCTTCCA CTTTTATGGT 780
TCTCTGTTCC TCACTGAGCT TTGGGTATAA GGCTGTAAGA TAGGGCAGAG GCCAGTGGAT 840
GCTTTCTCCC TGATAACTGC ATTCTGCTCT CTGTGCTTCT CTCTCTAGAG TGCCCAGAGG 900
GGTGCGGGGC CTGAGAAAAA GCAGACCCAG GGCAGAGAGA GCACCACCCA AGCTGCTGAC 960
TATAATAAAT GGCAGGGGCT GGGGACTGGA AGGGGTACCA TATGGTTGTC TTCTGATTAC 1020
TTTCAAATGG AATCAGACTC AAGCCTAAGA GAGAGAGTGG GGAGAAAAAA CCACACTCAA 1080
GAATGGATCC TCTCTGCAGG GTGACAGACT CAGCCAAGCA GAATGCAGAG CCATTGCCAG 1140
AAGAATGAGA TGACTATGAT CCTCATTGAA 1170
|
