| Tag | Content |
|---|
EnhancerAtlas ID | HS098-00008 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:958550-959840 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr1:959249-959260 | TGGGTGTGGCT | - | 6.14 | | NR2C2 | MA0504.1 | chr1:959093-959108 | TAGGGTCAGAGGGCA | + | 6.37 | | SP1 | MA0079.4 | chr1:959247-959262 | GGTGGGTGTGGCTTA | - | 6.01 | | ZNF263 | MA0528.1 | chr1:958958-958979 | TGAGGAGGGGCTGGAGAAGGG | + | 6.18 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_57930 | chr1:958868-959111 | VACO_9m | | SE_57930 | chr1:959358-960218 | VACO_9m | | SE_69072 | chr1:955444-963640 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 959012 | 959267 | | chr1 | 958662 | 958759 | | chr1 | 958905 | 958959 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I001023 | chr1 | 958815 | 961479 |
|
Enhancer Sequence | GGTCTGGAGA GTGCTTCCTC CTCAAGGCAA CGGTAAGGGT CCTGACTTCC CGTCTCTCCG 60
ATCTGCTCCG TTGGCCGGCA GGAAACTTTG CTGCCCTGAC ACTAGCCTGG CTCTTGAGGG 120
GTCCTTGTGG GGTCCTGGAC TGTCCACTGC TCTTGCCTTC TCTGTGCATG CCTGGGGGCT 180
ATGCAGGGGG AGGGGCAGCA CCCAAAATAA GGAACGCTGC GGCCTTTTCC CCAGCCTGTG 240
GTCAGTGGTC CCCAAGCTGC CTTCAGGGTC CAGGGCCTCA GTGCAGCACA GAGGAGGGTC 300
CCCTGGGTCC CCCACTGGGA GGACATGATA ACCTTGGTCC TCTTCTGGGC ACTCATGGTC 360
TGGGGAAAAG ATGGGGGCAT CGTGGACTCA GGATAGGCTG TCAGGAGCTG AGGAGGGGCT 420
GGAGAAGGGG GTTAGGGCGA GGAGAGGTTC CTGTCCCTGC AAGATCAGGA GAGGGGGTCA 480
CTAACCCCAC AGCCAGGTGG GTCCAGCCCG AGAGTCCGTG ACTTAGTAGC TGAGGACTTG 540
CTCTAGGGTC AGAGGGCACA TGGCAGGAGA GTCACCCCGG CTGAACGAGG CTCTGCATCT 600
TACCGAAGCC GCTCTACGGG TGCCAGGCAC TGGCTCTGGA GCGAGTGCCC AGGCGGAGCA 660
GAGCGCTGGG AGGAGGGTCC GTGGGGAGCC CCTGCCAGGT GGGTGTGGCT TAGCCCAGCT 720
GTGGGCAGTC GCACTCAGGG ACGAGCTCCA GGTGGGGAGC CTGGGACCCA CAGCCAGTAT 780
GCAGCTTGGG GAGCACCCGG GAGGGGCTGT GGCCACCGGA CCCCCTGGGG TGGGGCTGGC 840
CAGGGGAGGG TTAGCCAGGG AGGACTGTCA TGGGAGGGGC CTTGCAGGTG AGCCAGGGGC 900
CAAGGGGAGC CTCAGGAGGG AAACAGCATG AGGAGTGGGG GAGCCCAGGA GCTTCCGGTG 960
GGACATGTGG AGCTCTGCTG TGGAAGTAGA CCAGGGATAT CTCGGGTGGC TGGGGTCCCT 1020
GGCTGCCGGG ACAGGGTAAA TGCCTCCCAG AAGCCTGGGG TGAGCCCTGA GGGACAAGGT 1080
CTCTGGAGCC AGTCTGGCTG GAGAAGGGAC AATTCTGTGT GCCCACCCCT CCCCTCACAC 1140
TGGGTGGTGT GGGAGGTGGG TCCATCTCCT GCTCTGTAGG AGATAAGGAC ATTGAACCCC 1200
ACCCTGGGCC CTCTGGTAGC CAAGGCCTCA CCCTAGTGAG GGGGATGGAT GGAGGGAGCT 1260
TGAGCCTAGC TGACCTCTCC CCATCTGACT 1290
|
