| Tag | Content |
|---|
EnhancerAtlas ID | HS038-21263 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr8:59770270-59771470 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr8:59770322-59770343 | ATTTTCTTTCTTTTTTTTTTC | + | 6.07 | | Nr2f6(var.2) | MA0728.1 | chr8:59770547-59770562 | TGAACTCCTGACCTC | - | 6.22 | | POU4F2 | MA0683.1 | chr8:59771392-59771408 | CTGCATGATTAATTAG | + | 6.31 | | TBP | MA0108.2 | chr8:59771302-59771317 | CGGTCCCTTTTATAC | - | 6.16 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_38326 | chr8:59767534-59771984 | HUVEC | | SE_45769 | chr8:59766693-59780524 | Osteoblasts | | SE_61177 | chr8:59757289-59812719 | HBL1 | | SE_63973 | chr8:59767634-59771822 | HSMM |
|
| | 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 |
| GH08I058855 | chr8 | 59767955 | 59772587 |
|
Enhancer Sequence | GGCACAATAT TAGCTACATA TTTCAGCATA TGTTTTCACT TTCTTTCCTT TGATTTTCTT 60
TCTTTTTTTT TTCTTTGAGA TGGACTCTTA CTCTGTCGCA CAGGCTACAG TGCATTTGCA 120
CGACATTGGC TCACTGCAAC CTCCGCCTCC CAGGTTCGAG TGATTCTCCT GCCTCAGCCT 180
CCTGAGTAGT TGGGATTACA GGCATGTGCC ACAACACCCA GCTACTTGTT GTATTTTTAG 240
TAAAGACAGG GTTTCACCAT GTTGGTCAGG CTGGTCTTGA ACTCCTGACC TCAGGTGATC 300
CACCCACCTC GGCCTCCCAA AGTGTTGGGA TTACAGGCGT GAGCCACTGT GACTGGCTCC 360
TTGGATTTTC TTTGAAAAGC AAAAGAAAAA TAAAAACCCT GTGCTCATCT CAGGTTATTA 420
TTTTTAAAAA ATGAGTAAGA TTTTGGTGTA ACTGGAATGG TGAAAAAAAA ATCCTTGGAA 480
TAACATTAGT CATGTTAGTG ATGAAATAGT GTTAAAATCA CATACTTGAA TGGCACCAGA 540
ACGATGGAGG GCCTGCCTTT CAGTGTTTAA AACTCTGTGT GCTTCACAAT CCTTCCAGAG 600
TCTGTATTCC TCCTTCAAGT ATCTGCATCC TTCCCCGTCC AACACACCAG CCTTGAAAGC 660
TATCATTATC TCTGCCTCTA GCAGACAATC TATATCAAAA CAGTTGTACA CATAAAACTG 720
CACCACCGCC TCGGCTGGCT CTGCTCTGAT CCAGCTGTTA GAGTGAATAG CAGTTGGTGC 780
ACAGAGCGCT GGAACATGGG TAGCCCTGAG GCCTTATTTG CTAATGTGGC TCACCAGCTG 840
CTGCTTTCTG TGGTCTTTGC AGGCAAGGCC TGGAAGGCTG CCAGTTGCAG CAGGAGCAGG 900
AGAACGTGAG GAATCTCTCA AGCCCGTCCA TTTACCCCTG TCTGTCAGCA TTTGACACCC 960
TGAGCTGTGG AGTGCTTTCC CCAGGGCAAT AAGGAGACCC TGCTGGCTTT AGCTGTGACA 1020
AGTGCTTCCT CTCGGTCCCT TTTATACACA CTATCAAACA CACACCGTTC ATAGCACCTT 1080
AAGAAAAACT TCTGAGCCTT GCTCTTGGCT GTCCATGCAG GCCTGCATGA TTAATTAGGG 1140
CAGGAAGGCA AAGCGGTTTC ATTTTTCTTA GGAATAATGC ACTCTAAGAG TCTATGAGAA 1200
|
