Tag | Content |
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EnhancerAtlas ID | HS022-01057 |
Organism | Homo sapiens |
Tissue/cell | CD4+ |
Coordinate | chr1:156480550-156481910 |
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) |
Ar | MA0007.3 | chr1:156480736-156480753 | GGGAACAGGGTGTGCTT | + | 6.5 | ZNF263 | MA0528.1 | chr1:156481554-156481575 | GGAGAAGGTGGGGAGAGAAGA | + | 6.11 | ZNF410 | MA0752.1 | chr1:156480985-156481002 | AATAGCCCATAATACTT | + | 6.22 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_01624 | chr1:156477283-156481289 | Aorta | SE_03183 | chr1:156477551-156481259 | Brain_Angular_Gyrus | SE_04925 | chr1:156477350-156481357 | Brain_Cingulate_Gyrus | SE_05851 | chr1:156477083-156481717 | Brain_Hippocampus_Middle | SE_06826 | chr1:156477528-156481358 | Brain_Hippocampus_Middle_150 | SE_07824 | chr1:156477281-156481720 | Brain_Inferior_Temporal_Lobe | SE_25856 | chr1:156477061-156481377 | Duodenum_Smooth_Muscle | SE_26648 | chr1:156477421-156481272 | Esophagus | SE_29623 | chr1:156479942-156481322 | Fetal_Muscle | SE_31445 | chr1:156479965-156480889 | Gastric | SE_34669 | chr1:156477332-156482747 | HeLa | SE_37054 | chr1:156477240-156481638 | HSMMtube | SE_40614 | chr1:156477084-156481316 | Left_Ventricle | SE_42136 | chr1:156477223-156481291 | Lung | SE_44813 | chr1:156480038-156481327 | NHLF | SE_46671 | chr1:156479512-156481207 | Ovary | SE_48054 | chr1:156442802-156481304 | Psoas_Muscle | SE_48054 | chr1:156481399-156482547 | Psoas_Muscle | SE_48580 | chr1:156477233-156481289 | Right_Atrium | SE_50090 | chr1:156477346-156481284 | Sigmoid_Colon | SE_51078 | chr1:156456787-156481370 | Skeletal_Muscle | SE_52473 | chr1:156479756-156481261 | Small_Intestine | SE_53429 | chr1:156480159-156481292 | Spleen | SE_54540 | chr1:156476974-156481729 | Stomach_Smooth_Muscle | SE_61431 | chr1:156449469-156496609 | Toledo |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I156511 | chr1 | 156481561 | 156481710 |
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Enhancer Sequence | GCTGGGGAAA TGATGAGGGT TGGGTTCCGT GGTGGCCGAC ACCCAGCCCC TCCTCCACAG 60 TGCCTGTCTC CTTGCTGGTA TCTTGGCAGG CTCCCGTTCT CCCATCAGAC GCTACACTCA 120 CACATGCTGC ACATACTGGT GAATAGCTTC TTGCAGTCCA TCCTGGCACG GTCCCCAAAT 180 TCCGCAGGGA ACAGGGTGTG CTTCAGCCCT CTCCCTCTCT CACTAAGGGC TAGGAAGTTT 240 TGAGTCTTCC ATCTCACACA CCCCAGAGGC TGCGTTGCCG AGAAGACACA GGGGCAATGT 300 GAGGCCTTCT TATTCCTGAC CCACGAGAAC GATGCCAAGT TGGGGACAAG AAGGGTAGAG 360 GCTTGTTTTG CTTTCATTCC TGCTTTATGC CAGGCACTCT GAAAGGCATT GTGTACACTA 420 TTTTCATCAT CAGACAATAG CCCATAATAC TTTGTCTGAC ATCTGACAAA GAACGATCAG 480 CCTCATTTTA CAGATGGTGA AACTGAAGGA GCATGTTCAT GTTCATACAG CACAAAGTGG 540 CTCTGGGATT TCAACCCATA GAGGAGTGTT AGAATAATAC CCTCACAAAT TCAATGTTGA 600 AAGTGCTAAT GAAGTCCGGG CGCGGTGCCT CATGCCTGTA ATCCCAGCAC TTTGGGAGGC 660 CAAGGCGGGC AGATCACCTG AGGTCAAGAG TTTGAGACCA GCCTGACCAA CATGGAGAAA 720 CCCCGTCTCT ACTAAAAATA CAAAATTATC CGGGCGTGGT AGCACATGCC TGTAGTCCCA 780 GCTACTTGGG AGGCTGAGGC AGGAGAATTG CTTGAACTTG GGAGGTGGAG GTTGCAGTGA 840 GCTGAGATTG CGCCACTGCA CTCCAGCCTG GGCGACAGAG CGAGACTCCA TCTCAAAAAA 900 TAAATAAATA AATAATAAAT AAATAAAATA AAAAAAGTGC TAATGAGACA GAAAAGGGCA 960 CTGAAAGATC CGGTCACCCA GGGACCTCTC AATTGCTCAG ATTTGGAGAA GGTGGGGAGA 1020 GAAGATTGCG TCAAACAGAC CTGAGATCCG ATCCCAGCTC AGTCATTTCC AGCTGTGTGA 1080 CCTTGGGTGA GTCACTCGCT TTTTCTGAAT CTCGGTTTTC TCAATGATGA TGTGACAGCA 1140 ATGTTCATGA GGTGCTGCCA AAATTACAAT AGATCATGTA AACTATGTGC AATGTACTTC 1200 GTTGCCTTGC AGCAATGGAT GGCGCCTCTC CTTCCATCCT CTACAGAAGG AGGAAGAGGT 1260 AAGCAAGAAC AAATTCAAGA GGGTGCAAAT CTGCTGGTAT AGTATCAGGA AGCCCAAAGC 1320 CTGGCAGAGG TTTGTAGAAC AGGCAAAGGA TAGCAAAAGG 1360
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