| Tag | Content |
|---|
EnhancerAtlas ID | HS187-18756 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr4:101941880-101943110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr4:101942142-101942160 | CCTACCTCCCCTTCTTCC | - | 6.42 | | Foxq1 | MA0040.1 | chr4:101942238-101942249 | AATAAACAATT | - | 6.02 | | JUN(var.2) | MA0489.1 | chr4:101942309-101942323 | AGGAAATGACTCAT | + | 8.12 | | ZNF263 | MA0528.1 | chr4:101942133-101942154 | TTCTCCTTCCCTACCTCCCCT | - | 6.28 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_34558 | chr4:101939290-101944846 | HCT-116 |
|
| | 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 |
| GH04I101017 | chr4 | 101939061 | 101944005 |
|
Enhancer Sequence | AGAACTGAAA TTTAAGTTAG CTTTAGAAAT AAATTGGACT AGGTTTCTCA AACTTGTCTG 60
ATCCACAAGA ATTTTGGTGG ATGCTTATTA AAATGTAGGC TCCACTCCAG ACCTTTGGGG 120
ACCAGGAAAT TCTTACGAGA AAGAACAGGT AACATTGAAC TGGGGTAAGT GTTTCAGCTG 180
CTCTTCAATA ATGGTTTGCC ATTTGGAATC TGGGAGTGCC CACACCATAA GGTCATGCCA 240
AAAAATATTT TATTTCTCCT TCCCTACCTC CCCTTCTTCC AAGAAACACT ATGCCAGGCA 300
GTGTTTCATC CTAAGAATGC AAAGATAGCA ACAATGCTCA CTGCAGTGCC AGACAGACAA 360
TAAACAATTA CATGCAGTGG ATTAAGTGTC AAAACGGAGG TAGTACAGGA TACTGTGTGC 420
TTAGAGAGGA GGAAATGACT CATTCCAGTA TTTAAGACAC ATCTGAAATC TGCACATAGA 480
AGATGCATGA ATACAGACCC AGAGAATTGA GGAAGCCTGG TGTCTTCCGA ACATTGTGAG 540
AAGTCCACTA TGGCCGAAGC TCAGGGTCAA GTTTGGGGTA GATGAGATTG GCAGGAATCA 600
GATCGTGAAT ACACTTACAT GCCACCTTGT AAGACTCTCT GCAGGACAGT CCTGCAGACA 660
ACCTGGAGTT GTTGAGAAGC CTAAATGTTT CCAGCAATTG GTATAAAAAG ATTTGAAAAT 720
ATAACATGAC AAAAATGCCT TAGGGGAGAA GTTTAAGTCA ACTTTGTTCT AAGCTAATAT 780
TCTATAGTCA ATTAAAACTT TGATAATCTA GTGGAGACTC TTTTCAGCTG ATACACAGCA 840
AAAAACATAA AAGAGCTGCT TTGGTTGATG CAGAAAGCTC AGTCCCATGT CAGTATTCCT 900
GGAAATACAA GCTTCTAGCC AACAGTTTGC AAATCAAAGT TCTGTGTTTT CGGAAGACTG 960
AATAATTGCA TGGATATTTA GAATCTTACG ATTGAAGGGT AATTTAGATA TCACCTAGTT 1020
CAATGTCTAT CTTTGAAGAG AGTTTCTTCA ACTACATCCA GTATAACTCC TTCCAGGCAG 1080
CATCACTCAG GAGGTGTCTA GGCACTGAAT AAAGTTTGCC CAGGTTTTAA CACTTGCAGC 1140
AAAGGGGAGG CACTTGCACT CTCCTGCAGC TTACTCTCTG GTTAAGCAGA GTCATTCCTT 1200
AAGCATCTAT CCTATGGTAA TTAGGCATCT 1230
|
