| Tag | Content |
|---|
EnhancerAtlas ID | HS100-00192 |
Organism | Homo sapiens |
Tissue/cell | HT1080 |
Coordinate | chr2:230309250-230310680 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXH1 | MA0479.1 | chr2:230309980-230309991 | CCGAATCCACA | + | 6.02 | | KLF4 | MA0039.3 | chr2:230309458-230309469 | GCAGGGTGTGG | - | 6.62 | | Nr2f6(var.2) | MA0728.1 | chr2:230309388-230309403 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_56283 | chr2:230308291-230312096 | u87 |
|
| | 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 |
| GH02I229443 | chr2 | 230308672 | 230311461 |
|
Enhancer Sequence | AAAAACACTA TTTATCTCTA ACTCCCTTCA ATTTTAAGTT TTAGAAATCA ACTAACTATA 60
AGAAAAAGTT TGGGTCAGGC ATGGTGGCTC AGGCCTGTAA TCCCAGCACT GTGGGAGGCC 120
GAGGCAGGCA GATAACCTGA GGTCAGGAGT TCAAGACCGG CCTGGACAAC ATGGTGCAAC 180
CCTGTCTCTA GTAAACATAC AAAAATTAGC AGGGTGTGGT GGTGGGAGCC TGTAATCCCA 240
ACTACTTGGG AGACTGAGGC AGGAGAATCG CTTGAACCCG GGAGGCAGAG GTTGAAGCCT 300
GGGCAACAAG AGCAAAACTC CATCTCAAAA AAATTTTAAA AAAGAAAAAG TTTGATATAA 360
TTAAGAAAAG AAGTCAGAGG AGAAAGGGAG GAGAAAATAA AGTTGTTTTC TGGTCTTACA 420
ATATTTAATT CTTCTTTGTG GGGCTTCACA GAGAGAACGG AACTCTCAGG AGACAGGTAA 480
TAAAGTATTA AGGAAGTTTT TGTTCAGAAT GCTGCTGAGG GGTATTTTCA CATGTGTTAC 540
GACATCCAGA GCAGAGCTGG GAACAGCGTG CTCGTGAGTC AGTACGTGAG TAAGCCTCTG 600
TTCTTCCAGC ACAATTGCAG CTTGTTTAGT TTGCAAACAC AAGTTGTCTC AGTGATCCAC 660
ATTCCCAATA GGTAAGGGCC AGCGCCACAC TGCCTCCTCC CACAGGACAC GCAGCTCACA 720
GCATGTGAGC CCGAATCCAC ATGGAAGAAA ACTGGACCCT CTGAGGGGCA GCTATTCCTG 780
TCTCCACCCT GGCTCTGAAG GAGAGCATGG AGGTCAACCA AGAAAAATAT CCTCATGTCA 840
AACACAGTGG AGAAACTGTT TCACTTCAAG GTTTATGAGA TCCAAAAATG TTACTGCGAT 900
AGTTCATTTC GGGTGTCAAC TTGGCTAGGC CATGGTTCTT AGATACTCGC TCAAACACTA 960
ATCTAGATGT TGGTATGAAG GTGTGTTTTA GATGAGATTA ACGTTTAAAT CAGCAGACTT 1020
TGAATGAAGC AGATGACTCT CCAGAATGTG CGTGGGCTGC ATCCAAACAG CTGAGGACCT 1080
TAAGGACAAA GACTGAGGTT TCCCAAAGAA GAAATAATTC AGCTCAAGAC ACAACACAGA 1140
AACCTCGCCT GAGTTTCCAG CCTGCCAGCT TCCCTACGGA TTTTGGACTT GTGAGTCCAC 1200
ACAATTGCAT GAGCCAGTTA CTTAAAATAA ATCTCTCTCT CTCTCCTCGC TCTCTGTCTC 1260
CTGTTTCTCC GGAGAATCCT AACTACTAAC ATTGTTACAA AGCAGATTAA ACAGCCCTAT 1320
TCCCTCTGAA TGTCAGAGCA GAGAGGAAAG AGGCACTTGG CAAAATATCA GTTGCTTAGA 1380
AAATCGGGGA ATTAAGAGTC TATGTGAAAA AAGGCTTTTC AACACCATTC 1430
|
