| Tag | Content |
|---|
EnhancerAtlas ID | HS197-06693 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr14:70484670-70486080 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr14:70484924-70484942 | GCAAGGCAGGCAGGAAGA | + | 6.13 | | EWSR1-FLI1 | MA0149.1 | chr14:70484920-70484938 | GGGAGCAAGGCAGGCAGG | + | 6.27 | | EWSR1-FLI1 | MA0149.1 | chr14:70484916-70484934 | GGAGGGGAGCAAGGCAGG | + | 6.33 | | IRF1 | MA0050.2 | chr14:70485819-70485840 | GAAGCAAAACTGAAAGTGCTG | - | 6.62 | | Nfe2l2 | MA0150.2 | chr14:70484879-70484894 | TGCAGAGTCATCCTG | - | 6.57 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_34800 | chr14:70483069-70486381 | HeLa |
|
| | 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 |
| GH14I070018 | chr14 | 70485118 | 70486244 |
|
Enhancer Sequence | TCCAGCAGAG GGGACCATGT GGGTAGTGAG GTGTGAACAG GGTAGGAAGT GTGGAAGGAA 60
TTGTAAGAAG TAGTATGGTT TATGTTTGGG AGTCAGGCTG GGGACAGGTA GGAGATGAGG 120
CTGCAGAGTT GAGCAGAGCC CAGCTGGTGC CAGGCCCTGG GAGTCAAGAT GCAGGGCAGA 180
AGGGAGCTGC AGGGTTAGGT GGGCATTTTT GCAGAGTCAT CCTGATGGCA CTATGGAAGC 240
AGGATTGGAG GGGAGCAAGG CAGGCAGGAA GACGATAGCA AGTGTCAGCA TGAAGGGTGA 300
TGAGGGCATG GACCGTGGGA AAGGGATGAT TTGCTGAAGC TTTTGTAAAG AAATCAATAG 360
GATTTCAAGA CTTGCTACAT GCAGGGAGTA GAAGAGTGGG AGGCATCTAC TCCCTTTTCT 420
GGCCTGATTT ATTAGCAAAA AACAGTGCTA CAAAGATCTA AAAATAGGCA GAGTAGAATG 480
GGGTGTCTGT GAAAACTCTA TGGCAGGTGC GTGGGAGGGT GTGCATTGCA AATATCAATG 540
GATGATAGTC CCTCTTGGTG AATGTTTTCT GTGTGAGTGA GTTATCCCTT TGGCCCCTCT 600
GGCCAGGGCT CCAGGAGGCA GTGTTCCCCC TTAGAACAGC CTTCCCACAG CACCCATTAG 660
CATTTATCAG TCCCAAAGGA AGATTTCTGA GATCTCAGCC GGCAGAGTCT TCTAGAGCAG 720
GGGAACCCTC TCCTGGCTTC ACCCTCCCCC AGGGAAAGTC AACTTTGAGG GGAGGTGGGA 780
AGGGCTGTGT GAGCCTCTTG GCCCTTCACG TGGTCCCCTG AGGGGAGACT GTACTGTGGC 840
TTCCTCCTTC CTGCCCAGTG TGGTTGCCTG TTGATGGCTT TGCAAGGAAG AGGCTGGAAT 900
GTGGCTGACT TGGCATTTCC CAGCCGCACC CGCACAGCTG GCGGGGCCTG GACCCAACTC 960
CAGACGGGGC TCAGTTGGTC TGCTTGGCTT GGCTAGTGCC TCCAGGCCGT CCCGCCTTAC 1020
CTTCTCTAAA ACTGCTTAGG ACAGCAGAAC TGGGCCCGAG ATCTTGGCCA AAGCAGGTTT 1080
CCTTGTGGTA AACGGAGCTG GCTCTCCAGC TGTGCATTGC AGCCAAGGCC TGGTGGGGCT 1140
GAGGCTGCAG AAGCAAAACT GAAAGTGCTG TGGGAGAAGT GTAGCCTATG CCACCTCTGA 1200
AACTGGGAGA AGGCTCCTTG GGGCCAGTTT GGGGAGGAAC TTGGCTCTAG TGGGTTTCCT 1260
CATCCCTGGA GGCAGAAGTC AACAGGACAG TCACAAAAAC AGCCCAGAGG TAGGGCAGAC 1320
ACCAACGTTA TTTGGCTTAT GTTGTCTGAA CCATAGTCTT CTAAAATCTG GAATCTGGTA 1380
TCATTTGGGT GTGTCTTTTC ATACCATATC 1410
|
