| Tag | Content |
|---|
EnhancerAtlas ID | HS098-37122 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr22:40616230-40617360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr22:40616361-40616371 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr22:40616361-40616371 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr22:40616361-40616371 | ATTTTCCATT | + | 6.02 | | STAT3 | MA0144.2 | chr22:40617016-40617027 | TTTCTGGGAAG | + | 6.02 | | Sox3 | MA0514.1 | chr22:40616672-40616682 | CCTTTGTTTT | + | 6.02 | | Sox3 | MA0514.1 | chr22:40616796-40616806 | CCTTTGTTTT | + | 6.02 | | ZNF263 | MA0528.1 | chr22:40616475-40616496 | TGGGGAGGAGGGGGGGAGGGG | + | 7.2 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_18406 | chr22:40610608-40617062 | CD4p_CD25-_Il17-_PMAstim_Th |
|
| | 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 |
| GH22I040220 | chr22 | 40616005 | 40617703 |
|
Enhancer Sequence | TTGTTGAAGG ATCCCCAAAC CCTTGATAGC CATGGACAGC CCACAGTGGT CATGGAGCCG 60
GAGCCAGAAT GTAATTCCCA GTGTGACCAG GAGCTAGAGT TTAAGTCAAG GCAGCAGGTA 120
TACTCAGGTG CATTTTCCAT TCCCTTTGAG GGAGGGGTGG AGGTTTGAGC CCCCTCCACA 180
TCCCACCCCA TTGGGGTGCC TTTGTCACTC TTGACAGCTT TAGAGTGACT TAGATGGGAG 240
ATTGGTGGGG AGGAGGGGGG GAGGGGCACT GTTTGAATCT ACCCTGCTGG AGGCACTGAA 300
TAGTTTTATA AGTATGTGTA CACTCTATTG TTCAAGTGTT TGCTTAAATC ACTGTATCTT 360
CTTAGAAATT TTTGTAACCT TTTGGTTAGC ACTGTTACAG TTTAGTTTTG ATGCTCGGTG 420
TTTCATTTCC CATCTCCTTT CACCTTTGTT TTTTAAAAAA GCAAAAGATG CACGTAAAAC 480
AGTGGAAAGC TTAACTATAG AAACCCCGAG TTGGCCAGGA GAATTGGCAG GCGCTTGCTT 540
TCTTCACTTT CCCTTCCCTT TTAAAGCCTT TGTTTTAGGA AAAAGGAAAT TGGTGTGTTT 600
GGAGAGCAGT TGTTAGCTTT TCAAGACTGG ACTCGTTGGT CTAATTTGGT AAGGGCCCAG 660
AACACGTCCC ATGAAGTAAG GGAAAAATGT GAAGCTGAAG CCGGCATGTG GGGGAGAGCT 720
AACAACTGGA CATTTTCACC CAAAGCCCCG CCTCACATGC CTTTAGCCAG AAGGCTTGGC 780
TATTTATTTC TGGGAAGCTT TAGGTTTCCT ACTGATGATG GCATCCCCCC TGGTGTCTGG 840
GATGTTCCCT GCCCCTCCCT CCCAACTCTG TCGATACCTG TAGCATTCCT TCTTGGGTCT 900
GGGCACTGAG TCCAGGCCAT GTGTGGAAGA TTCCAGTTCT TTCACCATTC CATGTGACAC 960
AGCATGGCGG GTAGTTTCTT TTTTGTCAGG ACAACTGTTT CCTTCTTTGA GGTGTATGAA 1020
TGGTTTGTAG TACGTACCTG GGTTCCTAAG ATAGATCTCG ACTGTCTAGC CTGAGTGTCT 1080
AGCTATTTCA GGAACAATGT TGCTACACCA GTTGAGTGCT CAGGAACTAG 1130
|
