| Tag | Content |
|---|
EnhancerAtlas ID | HS105-23966 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr14:50484530-50485840 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr14:50485250-50485267 | CAGGTGATCCTGACCTT | - | 6.17 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_27688 | chr14:50484382-50485927 | Fetal_Intestine | | SE_28581 | chr14:50484353-50485967 | Fetal_Intestine_Large | | SE_33820 | chr14:50484230-50485757 | HCC1954 | | SE_43464 | chr14:50483692-50485116 | MCF-7 | | SE_43464 | chr14:50485277-50487542 | MCF-7 |
|
| | 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 |
| GH14I050017 | chr14 | 50483911 | 50486982 |
|
Enhancer Sequence | CCAGGTCTGC CCTCAGAGAC TTCCAGAAAA GCCTTCCTCT CTGTCACTTT GCCTGATTCG 60
CCATTAGCAT TCCTGCAGCA GGTCAGCAGG TCTTGGGTAC CCAAGTTCCA GCTACATGAG 120
CTATAAAATC CCAAGCAGAA CTGGAGCATC AAATTGCTGT GGGTTCATTT TTGGCTGGCA 180
GGCCTCTTCT ATTAGCACCA TAAACACCAC CACTATCCCC ACAACACACA CAGAGAAATA 240
CAGCCTGAGG ATAAGAAGGC ACATTGAGGA GCTGAGGGCG CTGGTGAGGA GGGGACTGGT 300
CCACTAGCCA TGACGAGGAA TCCCTTTACA AAGGGGCCAG CTTTGATGTG GGAGTGGAGC 360
AGGGAAATCT AGAAAGCCTC CATCAGAGAC GGAATCCAAG ACCTGCAGTC CCAGGACTCT 420
GGTTCTGTTT AGACTCTTAG GTTATTCCTC CTTATGGGAA ATCCTGGAAC TGGACCAGCT 480
TCTGTGATAA CCTGCAACCC TGGGGACACA TTCAATTTGC AGATGTGTTG CACAATATTG 540
AGCAAAGGTT GATTCAACAT TTATAAGCTG GGAGTCGCAG ATTCATGGCT TCTTTTGGAG 600
AAACAGTAGG TATTGGTACC CCAGGCCCTC GTGGCCAAAT AGACTGGGCC TTTTAAATAG 660
AGTGAATGAC TCACAAGTTT GCACTTTCCA CCGCTCCCTG TGACAGCCCT CATAAGAGGC 720
CAGGTGATCC TGACCTTGCA CGTGCACTGC TGTTTATTCT TATAGTGGAA AAACGTTTCT 780
CTGTATACTC ATTGCCATCA AACGTGATTT CCCACACAGG ACTTCCCTGA CTCCTGAAGG 840
TATTTGATTT TGCAACCCCT GATCTAAAGC GCCTTGATTA GCCTGGATTG TTTCAATCAC 900
AAGGGATGGA AGATAAACCC ATCCAATTTA AACAAAAATA AAAAGAGAGG CTGACAGGCT 960
CCCGGTGCTG GGAAGGATTC CTGGGCAGTC ACAGAATGGA AGGAGGGACT GCAGGAATCA 1020
CAGAAAATGA CCAGTGAACT CTGCCAGGAT TCTGTCTCCA GCTCTCCTTC CTGCCTGTCT 1080
CTGTCTTTGG ATGTTGGCCT CATTCTCTTT CGGCAGAGAC GCCTTTGCCA CGTGGTGAGG 1140
ATCATGGCCA CCAGAAGTCC CAATTTAGAA ATCCCAGTAG AAAAAAGAGC TTCCTGTCTC 1200
CAGTTCTGAA AATCAATCCC AGGAAAGGAT GCTGGCCTCA CTTGGGTCAT ATGCTATAGA 1260
GCTGAAGGCT ATTTTCTTTT CAAATCAAAC ACTTATGTAG CTAGTCACTG 1310
|
