| Tag | Content |
|---|
EnhancerAtlas ID | HS034-16069 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr2:26220470-26221050 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr2:26220971-26220992 | CTTTTCTTTCTTTTTCTTTCT | + | 6.3 | | IRF1 | MA0050.2 | chr2:26220994-26221015 | TCTTTCTTTCTTTTTCTTTTT | + | 6.87 | | IRF1 | MA0050.2 | chr2:26220975-26220996 | TCTTTCTTTTTCTTTCTTTTC | + | 6 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_26712 | chr2:26220231-26221007 | Esophagus | | SE_28420 | chr2:26220324-26221531 | Fetal_Intestine | | SE_29154 | chr2:26220039-26221556 | Fetal_Intestine_Large | | SE_32014 | chr2:26220291-26221047 | Gastric | | SE_35193 | chr2:26220282-26221276 | HeLa | | SE_36382 | chr2:26220312-26221288 | HMEC | | SE_57610 | chr2:26220451-26220707 | VACO_503 |
|
| | 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 |
| GH02I025997 | chr2 | 26220270 | 26221869 |
|
Enhancer Sequence | GCGCCCAGCC AAACTTTGCT CTTTCTTAAA TCTCAGAGTG GGACTGCCAG TGCCAGCCTG 60
GCATTCCCTC TTGAAATCAT CACCTATTTC AGAGGAGGCT GCTACAGTGG GAAGTCAGGA 120
CAACAAGGTT GGGGCCAAAC TCTGGTCTCC CAGGCATTTC ACCTTAATAG GAAAAGTGCC 180
TGAATCTGTC CTCCTCATTT GGCTCATGTG CAGAACAAGG CACAAAGCCC TGCGTCTCCC 240
GGCTGCCTGT CCGATGCCCT TTTCCCTGAC TCACCGTCAA TCAGCAGTCA GACCAAGGTC 300
CCTGACTCAC CGTCAATCAG CAGTCAGACC AAGGTCCAGG CTCTTGCCTC CTGAAATGTT 360
GCAAGGGCGG TTTCCCAGTG TGATTCACAA ACAGCAAGAA TGTTTCAGGC TGACTTGGAG 420
ACCACTTGGG GGTGGTATCC TCAGCCAGGA AGCTTCCTCA GGGCCTCTGA GTCCCAGAGA 480
GCTCTATTTG TCTCTTTCTT TCTTTTCTTT CTTTTTCTTT CTTTTCTTTC TTTCTTTTTC 540
TTTTTCTTTC TTTCTTTCTT TCTTTCTTTC TTTTCTTTCT 580
|
