Tag | Content |
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EnhancerAtlas ID | HS030-01000 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr1:54742350-54744830 |
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 | CGTCTCCACG AAGCCACTGG AACAACTGCA GAGTAACTGT TGTGGAACAC AGATCTGGCC 60 AAGACATTAT CCAGCCCAGA GTGCTGCCCT GGCTTCCCAC TGCCCACTGG ATCAAGCCCA 120 TACTCAACAA GGTCCTTCAA CAATTGCCCG GCAACCTCTC CAGCCTCATC TCCCGCTGAG 180 CACCTGTCAA CCACCTCATT CTAGACACCA TCTCAGCCAG GGCTGCACTG CCTCCAGGAA 240 TGCCCTCCTG ATTTCTCAGC TTGGCAGACA GGCCTCTCCT GTGTCCTGCC ACAGGGGATG 300 GGTTACCTGT CAGTCTCTCT GCTAGGCTGG CTGCTCCTGT GGGCAGACTA TGGTTGATTC 360 AGTTCGAGCC TGGAACCAAG CCCCATGCCT TGCATATCAG AGACGGTCAA TGACAGTCAT 420 AACCACAGTC CTTTCTCCTT CTGTGACTTC ATCTCCCCAT CTATAAATGA GAAGCTTGGA 480 CTACATCAGG GATGGCAAAG AGGATATGTA CCACCACCGA CACATTCACG TTCATGGTAG 540 ACATTGCCAG TCACTATCTG TTGAGCCTGG ACACACAGCT TCAGAATCAT TCTCACGGTG 600 TTCTCAGCAG CCACCACACA TCAAGCAGAG CTGGCATTTG AATGGGGACT TCTTTGCTAC 660 TTCTTTAGAT AAGAGTTATG GTTTCTCTAT CTCCTTTCGG TCTCTCCCTC CTTTTATCTA 720 ATTCTCTACT CTCCCTGCTT CCGCCATCCA ATCAGATGTG CATCCACATT TGGACTTTGG 780 AGTGTTTGTG GAAGAGCACC CCATGAGGAA CCAGGAAAGC TGGGTTTAGA CTCTGATTAC 840 AGCCCCTGGT TAACTTGGGG CAAGTCATTC ACCTTTCTGA GTCTCACTTT CCCAATCTGC 900 ATGCCTTCTC TGCAGAAACA CTGTGATGAA AATGAAAGTA AGTTGCATGT TTAAAAACAC 960 TATGTAACTG AAAACAACTA TTGGAATTTA AAAACAAAAC AAGAAGAAAA ACAGCCTGTA 1020 CCCAATGCTC AGTTCTCTAT GACCCCTGCC CTCTTGTGAG TCCCGTTTTG GACTTAGAAA 1080 TCCTTACTGG ACAGTGCCCT CCTTAGGACC ACCTTAGGGC CAAGGAACTT AGAAATTCTT 1140 ACTGGACAGT GTCCCCCTTA AGGGGGAACT AGGGAACCCA CCCAGATCAG TGAGGCTGGC 1200 CAAAGCCAAG CTGGGTTTGC CAGATGTGCA GCCCAACCGA GCTAAGCTGC GTGGAAAAAA 1260 AAAATGCCAC TGCTTGATTA TGTAAAATCC ATCTGGATCC AAAGCAGAAA ATCAAAGTTG 1320 GAAGGGCCCT CAGAGACCAC CTGGTCCAGC CTGCTCCATC TACTGGTGAG AAAACTAGGG 1380 TCCAGAGATG GGGAGCAACT TGCCCAAGGT CACTCAGCAA GTATGCGGCC AAGTCCTCTC 1440 TGTCCTTCCC TGCTGCAAAA CACCAGAACA CCACTCCTGA ACTCCCAAGC TGGCTTCCTG 1500 TTAGGCCCTC CCTGATCAGA ATGTTGGATC TAGTGCTTTG GGGCTGCCTG GGCTCCTGTT 1560 CTGTAATGTG AGCAATACAA ATAAACTCAG TTCAAACATT TACTAGGTCC TTAGTATATG 1620 CCAGGTGCTG GGGATGCCAA TATTAGGGCT TTTTTTTTTT TTAAAGGTGA GGTGTGGTCA 1680 GGTCAGTTTC CAAGCCATCT CCCTGCCAGC CCTTAACTTG CTACCAGAGA CATCTCATGC 1740 CACGGGACCA GACAGGTACT GCCCGCCTTG GAAACCTGGA CGTGGAAGAA GAGAAAGCTG 1800 ATGGCCAACC CTCATTGTGG GTGGCCAAAA CTTCTGACCC CAGGAGCTGA AGCCTGGCAG 1860 TCAGAGGCCT GCAGAAGCAA GGCCCTGTGT TGCTTACCGA GGGGCTGGGA TGGAGGTGGG 1920 CAGCTGCTCT CTCCCACCCA ACCCTGGAGG CCTGGGGCTT CTACATTTAG GACCAGGCTA 1980 GGGGTGAAGT CCTGACCTGA AAACTGGGCT GGCCACCCTA GGCCAGGGTC TGGCCATAGC 2040 TGGCTCAGCC ATCCCAAGCC GACTCCCTGG TGCAAAGCCT TTCTGCAGCA GAGCTTCCTA 2100 CCCAGGCCTT GGCCAAGCAG GGGAAGGAGT GCAATTGTTG GTAACAGATA AAATCCTCGA 2160 TACCATCTCT ATTTCCCTTC TAATATCAGA GTGGCCGGCT GCAATACTAG TGAAGGGCAG 2220 GGCCAGCAAT CAATAGCTAA TATTCCTGTT GTAAGCAGGC CTACTCCGGA AATGGGCAGC 2280 CAGTACCTCC TTCCAGAGAG ATACCCTTTC CCCTTGGCAG TGTCCCAGCC TGAGCGGTTC 2340 AGCATCATGG CCAGGAAGGA TCAGGCCAGG TACCTGGCCT AGCCCATCCC CCTGCATCTG 2400 ACTGATGGGG AAATGATGCC GGGAAGTGAG AGAAAGGAAT CACCCAACGT CACCCAGGAA 2460 GCAGAGAGGC CAAGACATTG 2480
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