Tag | Content |
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EnhancerAtlas ID | HS050-51726 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr4:88462550-88463780 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr4:88462923-88462933 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr4:88462923-88462933 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr4:88462923-88462933 | AATGGAAAAT | - | 6.02 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_03658 | chr4:88463339-88463839 | Brain_Angular_Gyrus | SE_08500 | chr4:88462253-88463614 | Brain_Inferior_Temporal_Lobe | SE_25841 | chr4:88461128-88463620 | Duodenum_Smooth_Muscle | SE_29866 | chr4:88461110-88463833 | Fetal_Muscle | SE_54577 | chr4:88461013-88464194 | Stomach_Smooth_Muscle |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 88463626 | 88463762 | chr4 | 88462677 | 88462763 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I087539 | chr4 | 88461063 | 88463637 |
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Enhancer Sequence | CGGAGGAAAT GCAGTAAAAA TCTTTATAAT TATAAGCTTT TTGTCCATGT TGTTAGCGCT 60 TCTCATGTTG TGTGCTAAAG TTGGTTGAGA TCTGTAAAAG CACAGGACAA ATATTTCCTG 120 CACATGCCCT TTTTCATTCC TATGCTCTAA TCCCTGATGA AAGCCCCAAT CACTTCACGT 180 CTGACTGTTT TCCCTACCTC TGGACTCACA TTCACAAATG CAAATTGCCC TCAAGGGCCA 240 GGGAGGCCAC AGAAATTAAC GAAGGGGGCC CGAAGTAAGA AAACGACACT CTCCCAACAC 300 AGGCAGGGAT GACTGGCAGC TGACACATGG CCTTTGTGTT AGGAAGACAA GAGGGGGTGC 360 ATGGGACTTG GGAAATGGAA AATATGTAGT CCATCTGAAG GTGGCAGCTG CTACTCAATT 420 CTTGTAGCTT TATTGTCACA GGGAAATGGC AGCCCAACAT TGTCTGATCA TTTTACTGTT 480 TTAGAGAGAA ACCAGAAATC TAACATTTTA TGGGATTATT AAATATTGAC CAATAGTCTT 540 TGTGCCAAAT AAAACGGGTC TGTGAGCTGG GCTGGGCCAC TGAACACTAA GCTTTGAGCA 600 CAGTTCCAGA GACTTCCTTC TCTTTCCAAC CCAATCTATC TTAAACACTA TTTTAAACAA 660 TTTCACCCTC TCAAAGTGTA ATTCACATCA TGTTCCTCTC CTGCTTAAAA GTTTTCAATA 720 GCTTCCCACT GCCTACCAAG TCAATTCTAA ACTCGTGAGC CAGGCATTTT AAAGCCATCT 780 GCCACTTTAT GTAATATCTT CCCTTCACTT ATGTGAACAT CAACTTTTTC TCCTTTCCTT 840 GACTTACTTT GTAATTTTCT GCCTCACTCC TTTGACTAAG GTGGCTTCTT CTGCCTGAAA 900 CCTTCATGTT TAAATCTTAC CAATCTTTCA AAGTCGAACT TTAGATGTCT CCTTTCCAAG 960 AATCCTTCTT TGCTATATCT GATAAGAGGT TATTCTTTCT CTGAACTTCA ATAACGTATT 1020 ATTTTTGATA AAGTGTTTGG AACACTCTGC TCAGAGCAAG TGCGATAGGA CGAGTTGGCT 1080 CGGAAGGAGT GGCTCATCAC CCTCATTTGC CCTTCACTTC CCATCTCTGG CTCTGTCCTG 1140 TGTCATAGGG GAATAGCATA TTCATTTAAT TTTTTCTCTG GCATTTTTCA CTTTTCATTG 1200 TGTAATACAG AGTCCTCTAT CCCTTACTAG 1230
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