| Tag | Content |
|---|
EnhancerAtlas ID | HS076-32112 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr2:65058180-65059320 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr2:65058236-65058247 | TGCTGAGATTT | - | 6.32 | | HES2 | MA0616.2 | chr2:65058558-65058568 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr2:65058558-65058568 | GGCACGTGCC | - | 6.02 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_00723 | chr2:65057181-65060151 | Adipose_Nuclei | | SE_09303 | chr2:65057607-65060060 | CD14 | | SE_45951 | chr2:65057915-65060190 | Osteoblasts | | SE_53747 | chr2:65058097-65059464 | Spleen | | SE_57836 | chr2:65058163-65058646 | VACO_503 | | SE_57836 | chr2:65058678-65059568 | VACO_503 | | SE_62791 | chr2:65045447-65101119 | Tonsil |
|
| | 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 |
| GH02I064830 | chr2 | 65057483 | 65059973 |
|
Enhancer Sequence | CAGGCTGGTC TGGAACTCCT GACCTCAGGT CATCTGCCCA CCTCGGCCTC CCAAAGTGCT 60
GAGATTTCCC GCGCCCGGCC TTGTTTTGCA TTCTTACCGC CCCCTAGCCC CGTAACAGTT 120
TAAGGTTCCA GAGCAACCCC GCTGCTGTGA TGAACTGACT GAGACAACCC CTTTCCCCTT 180
GTGCTGTTTT CCAGGAAGCA CGTGGCTGCA GAAGCAATGA GCTCTTTGTG CCCTCTCTTC 240
CTGCTCCAGG GTTCCATGTG TCTGTGACTC TAAGCCTGGT GTGTGGACCG GGAAACATTC 300
AAACAAGGCT AAGAGAAGCC TGTCAGTCCA GCTCGGGCTA CACACTGGGT GAGCCATGCA 360
CCACCCAGGA ATTTCCAGGG CACGTGCCAC GTAAGGGGCA CACCCGACAG AGTCCAATGG 420
GGTTCCCCAC TGGGCCTCCC ACTGAGTTGC TCAGCCTGGG CCGGAAAAGG GTGAGTCACC 480
CTGGGGGTGG GGCTCTCCAG GGTAGAGGCC AAAGGAGTGA CTACCATGAC AATTCTCCGG 540
AGGGCCTGAG GCGGCGGTGG ACAGCCCCGG CAACAGTGGG CCCTCCCCGC AGAACTGTGG 600
TTCCAATCCC TCTCCACCCA GCCCAGGAGT CTCCTGGCCC CAGAAGGAGG AGCAGGAGGC 660
GCCAAAAAGA GGAAAAAGAA TTCCTTTTCC AGTCATTTCA GTCCTAAATT TTCCCTGAGA 720
CTGCCAGAAA AGATGCTAAT GAAAGACCAA TTGTGTGGCC AGAGTGTTTT CTTCGGACAT 780
CTGCCCAGGG AACTGGAGGA TACCCAGTTC AGAAGCGAGG TCACTAGCCC CATCCTATGG 840
CAACACCTTT TGCTCGCTAC TGACCCCTAC TGGGGAAGTG GAGACAAGCG GCTGAGGGCT 900
GGGAAGCAGC TGAAAGAAAC TAGACCCAGA CATGTCTACT GGGTTCTTAA ATCCAACATC 960
TGCTGTTGGA GGATGAGTCC TGCCTAAACC TTAGGCCACA GATGCAGAGG ATCTAACCTT 1020
GGGAATTCCG TTTCCTTCAA GGGGCCCCAA AACCTTTCAC ACTGGACTTC TCTTTTGCTT 1080
AACTCCCCTT AATGTTTTGT CCTATGGGAA ATGAGGAGCC TTTAAAGCCA GCTTGTCCAA 1140
|
