Tag | Content |
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EnhancerAtlas ID | HS045-01804 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr1:54742370-54744840 |
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) |
IRF1 | MA0050.2 | chr1:54743272-54743293 | GTGATGAAAATGAAAGTAAGT | - | 6.53 | NR2C2 | MA0504.1 | chr1:54743389-54743404 | TGACCCCTGCCCTCT | - | 6.43 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_01019 | chr1:54742220-54743317 | Adrenal_Gland | SE_01019 | chr1:54743357-54745653 | Adrenal_Gland | SE_01595 | chr1:54735208-54747683 | Aorta | SE_03451 | chr1:54742376-54744111 | Brain_Angular_Gyrus | SE_04901 | chr1:54742151-54747662 | Brain_Cingulate_Gyrus | SE_05919 | chr1:54734892-54749698 | Brain_Hippocampus_Middle | SE_07802 | chr1:54742248-54747743 | Brain_Inferior_Temporal_Lobe | SE_24580 | chr1:54742299-54743037 | Colon_Crypt_2 | SE_24580 | chr1:54743350-54744906 | Colon_Crypt_2 | SE_25961 | chr1:54737420-54746794 | Duodenum_Smooth_Muscle | SE_26701 | chr1:54737688-54747569 | Esophagus | SE_28122 | chr1:54742303-54745062 | Fetal_Intestine | SE_29698 | chr1:54742317-54744189 | Fetal_Muscle | SE_31383 | chr1:54733777-54747551 | Gastric | SE_41585 | chr1:54742296-54743306 | LNCaP | SE_41585 | chr1:54743339-54746155 | LNCaP | SE_42582 | chr1:54737622-54745972 | Lung | SE_46626 | chr1:54742299-54743302 | Ovary | SE_46626 | chr1:54743369-54746342 | Ovary | SE_47967 | chr1:54742267-54743053 | Pancreas | SE_47967 | chr1:54743288-54743925 | Pancreas | SE_47967 | chr1:54743996-54744556 | Pancreas | SE_47967 | chr1:54744577-54745034 | Pancreas | SE_50141 | chr1:54737715-54747690 | Sigmoid_Colon | SE_52383 | chr1:54737623-54747577 | Small_Intestine | SE_54182 | chr1:54736914-54745759 | Spleen | SE_54942 | chr1:54737059-54745949 | Stomach_Smooth_Muscle | SE_65414 | chr1:54736995-54742916 | Pancreatic_islets | SE_65414 | chr1:54743507-54745020 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 54743012 | 54743800 | chr1 | 54742604 | 54742755 | chr1 | 54742820 | 54744081 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I054271 | chr1 | 54736922 | 54747506 |
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Enhancer Sequence | AACAACTGCA GAGTAACTGT TGTGGAACAC AGATCTGGCC AAGACATTAT CCAGCCCAGA 60 GTGCTGCCCT GGCTTCCCAC TGCCCACTGG ATCAAGCCCA TACTCAACAA GGTCCTTCAA 120 CAATTGCCCG GCAACCTCTC CAGCCTCATC TCCCGCTGAG CACCTGTCAA CCACCTCATT 180 CTAGACACCA TCTCAGCCAG GGCTGCACTG CCTCCAGGAA TGCCCTCCTG ATTTCTCAGC 240 TTGGCAGACA GGCCTCTCCT GTGTCCTGCC ACAGGGGATG GGTTACCTGT CAGTCTCTCT 300 GCTAGGCTGG CTGCTCCTGT GGGCAGACTA TGGTTGATTC AGTTCGAGCC TGGAACCAAG 360 CCCCATGCCT TGCATATCAG AGACGGTCAA TGACAGTCAT AACCACAGTC CTTTCTCCTT 420 CTGTGACTTC ATCTCCCCAT CTATAAATGA GAAGCTTGGA CTACATCAGG GATGGCAAAG 480 AGGATATGTA CCACCACCGA CACATTCACG TTCATGGTAG ACATTGCCAG TCACTATCTG 540 TTGAGCCTGG ACACACAGCT TCAGAATCAT TCTCACGGTG TTCTCAGCAG CCACCACACA 600 TCAAGCAGAG CTGGCATTTG AATGGGGACT TCTTTGCTAC TTCTTTAGAT AAGAGTTATG 660 GTTTCTCTAT CTCCTTTCGG TCTCTCCCTC CTTTTATCTA ATTCTCTACT CTCCCTGCTT 720 CCGCCATCCA ATCAGATGTG CATCCACATT TGGACTTTGG AGTGTTTGTG GAAGAGCACC 780 CCATGAGGAA CCAGGAAAGC TGGGTTTAGA CTCTGATTAC AGCCCCTGGT TAACTTGGGG 840 CAAGTCATTC ACCTTTCTGA GTCTCACTTT CCCAATCTGC ATGCCTTCTC TGCAGAAACA 900 CTGTGATGAA AATGAAAGTA AGTTGCATGT TTAAAAACAC TATGTAACTG AAAACAACTA 960 TTGGAATTTA AAAACAAAAC AAGAAGAAAA ACAGCCTGTA CCCAATGCTC AGTTCTCTAT 1020 GACCCCTGCC CTCTTGTGAG TCCCGTTTTG GACTTAGAAA TCCTTACTGG ACAGTGCCCT 1080 CCTTAGGACC ACCTTAGGGC CAAGGAACTT AGAAATTCTT ACTGGACAGT GTCCCCCTTA 1140 AGGGGGAACT AGGGAACCCA CCCAGATCAG TGAGGCTGGC CAAAGCCAAG CTGGGTTTGC 1200 CAGATGTGCA GCCCAACCGA GCTAAGCTGC GTGGAAAAAA AAAATGCCAC TGCTTGATTA 1260 TGTAAAATCC ATCTGGATCC AAAGCAGAAA ATCAAAGTTG GAAGGGCCCT CAGAGACCAC 1320 CTGGTCCAGC CTGCTCCATC TACTGGTGAG AAAACTAGGG TCCAGAGATG GGGAGCAACT 1380 TGCCCAAGGT CACTCAGCAA GTATGCGGCC AAGTCCTCTC TGTCCTTCCC TGCTGCAAAA 1440 CACCAGAACA CCACTCCTGA ACTCCCAAGC TGGCTTCCTG TTAGGCCCTC CCTGATCAGA 1500 ATGTTGGATC TAGTGCTTTG GGGCTGCCTG GGCTCCTGTT CTGTAATGTG AGCAATACAA 1560 ATAAACTCAG TTCAAACATT TACTAGGTCC TTAGTATATG CCAGGTGCTG GGGATGCCAA 1620 TATTAGGGCT TTTTTTTTTT TTAAAGGTGA GGTGTGGTCA GGTCAGTTTC CAAGCCATCT 1680 CCCTGCCAGC CCTTAACTTG CTACCAGAGA CATCTCATGC CACGGGACCA GACAGGTACT 1740 GCCCGCCTTG GAAACCTGGA CGTGGAAGAA GAGAAAGCTG ATGGCCAACC CTCATTGTGG 1800 GTGGCCAAAA CTTCTGACCC CAGGAGCTGA AGCCTGGCAG TCAGAGGCCT GCAGAAGCAA 1860 GGCCCTGTGT TGCTTACCGA GGGGCTGGGA TGGAGGTGGG CAGCTGCTCT CTCCCACCCA 1920 ACCCTGGAGG CCTGGGGCTT CTACATTTAG GACCAGGCTA GGGGTGAAGT CCTGACCTGA 1980 AAACTGGGCT GGCCACCCTA GGCCAGGGTC TGGCCATAGC TGGCTCAGCC ATCCCAAGCC 2040 GACTCCCTGG TGCAAAGCCT TTCTGCAGCA GAGCTTCCTA CCCAGGCCTT GGCCAAGCAG 2100 GGGAAGGAGT GCAATTGTTG GTAACAGATA AAATCCTCGA TACCATCTCT ATTTCCCTTC 2160 TAATATCAGA GTGGCCGGCT GCAATACTAG TGAAGGGCAG GGCCAGCAAT CAATAGCTAA 2220 TATTCCTGTT GTAAGCAGGC CTACTCCGGA AATGGGCAGC CAGTACCTCC TTCCAGAGAG 2280 ATACCCTTTC CCCTTGGCAG TGTCCCAGCC TGAGCGGTTC AGCATCATGG CCAGGAAGGA 2340 TCAGGCCAGG TACCTGGCCT AGCCCATCCC CCTGCATCTG ACTGATGGGG AAATGATGCC 2400 GGGAAGTGAG AGAAAGGAAT CACCCAACGT CACCCAGGAA GCAGAGAGGC CAAGACATTG 2460 CTCTCTGCTG 2470
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