| Tag | Content |
|---|
EnhancerAtlas ID | HS050-20198 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr14:50484490-50486150 |
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 | | POU6F1 | MA0628.1 | chr14:50485979-50485989 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr14:50485979-50485989 | ATTAATTAAT | - | 6.02 |
|
| | 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 | AAAGATTCAG CAAGACAGGA TAGGTCTTTT ATGGCTGCCC CCAGGTCTGC CCTCAGAGAC 60
TTCCAGAAAA GCCTTCCTCT CTGTCACTTT GCCTGATTCG CCATTAGCAT TCCTGCAGCA 120
GGTCAGCAGG TCTTGGGTAC CCAAGTTCCA GCTACATGAG CTATAAAATC CCAAGCAGAA 180
CTGGAGCATC AAATTGCTGT GGGTTCATTT TTGGCTGGCA GGCCTCTTCT ATTAGCACCA 240
TAAACACCAC CACTATCCCC ACAACACACA CAGAGAAATA CAGCCTGAGG ATAAGAAGGC 300
ACATTGAGGA GCTGAGGGCG CTGGTGAGGA GGGGACTGGT CCACTAGCCA TGACGAGGAA 360
TCCCTTTACA AAGGGGCCAG CTTTGATGTG GGAGTGGAGC AGGGAAATCT AGAAAGCCTC 420
CATCAGAGAC GGAATCCAAG ACCTGCAGTC CCAGGACTCT GGTTCTGTTT AGACTCTTAG 480
GTTATTCCTC CTTATGGGAA ATCCTGGAAC TGGACCAGCT TCTGTGATAA CCTGCAACCC 540
TGGGGACACA TTCAATTTGC AGATGTGTTG CACAATATTG AGCAAAGGTT GATTCAACAT 600
TTATAAGCTG GGAGTCGCAG ATTCATGGCT TCTTTTGGAG AAACAGTAGG TATTGGTACC 660
CCAGGCCCTC GTGGCCAAAT AGACTGGGCC TTTTAAATAG AGTGAATGAC TCACAAGTTT 720
GCACTTTCCA CCGCTCCCTG TGACAGCCCT CATAAGAGGC CAGGTGATCC TGACCTTGCA 780
CGTGCACTGC TGTTTATTCT TATAGTGGAA AAACGTTTCT CTGTATACTC ATTGCCATCA 840
AACGTGATTT CCCACACAGG ACTTCCCTGA CTCCTGAAGG TATTTGATTT TGCAACCCCT 900
GATCTAAAGC GCCTTGATTA GCCTGGATTG TTTCAATCAC AAGGGATGGA AGATAAACCC 960
ATCCAATTTA AACAAAAATA AAAAGAGAGG CTGACAGGCT CCCGGTGCTG GGAAGGATTC 1020
CTGGGCAGTC ACAGAATGGA AGGAGGGACT GCAGGAATCA CAGAAAATGA CCAGTGAACT 1080
CTGCCAGGAT TCTGTCTCCA GCTCTCCTTC CTGCCTGTCT CTGTCTTTGG ATGTTGGCCT 1140
CATTCTCTTT CGGCAGAGAC GCCTTTGCCA CGTGGTGAGG ATCATGGCCA CCAGAAGTCC 1200
CAATTTAGAA ATCCCAGTAG AAAAAAGAGC TTCCTGTCTC CAGTTCTGAA AATCAATCCC 1260
AGGAAAGGAT GCTGGCCTCA CTTGGGTCAT ATGCTATAGA GCTGAAGGCT ATTTTCTTTT 1320
CAAATCAAAC ACTTATGTAG CTAGTCACTG TTCTAAGCAG GTCACGAATA TTAACTTATT 1380
TAAACCATAT TTTAAAGAGC CTATGAGTTA GGTGTCATTA TTGCCTCCAT TGCAAATAAA 1440
GAAAGTGAGC CCCAGAGATG TTAAGTGGCT ATCCCAAGGC CACAAAGCTA TTAATTAATG 1500
GAGTTGACAT TTGAAGCCAG CCAGCCTGGC TCCAGGGACT ATGCTTGTAC CCCATTGTAT 1560
GGTTGTGCAG GTTTGTACCA CATAACTCCA GGAAAGCAAC CACTGAACTT ACACAGAGCA 1620
TGACCTGTAC AGGTGTTGTG GAGAGCCTGC ACGTGCCTGA 1660
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