| Tag | Content |
|---|
EnhancerAtlas ID | HS105-02047 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr1:33829040-33831740 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat6 | MA0520.1 | chr1:33831048-33831063 | GGTTCTCAGGAAGGC | - | 6.03 | | Stat6 | MA0520.1 | chr1:33830914-33830929 | GTTTTCTTGAGAACT | + | 6.37 | | ZNF263 | MA0528.1 | chr1:33830290-33830311 | AGAGGAAGGGGTGGGAGAGAG | + | 6 | | ZNF263 | MA0528.1 | chr1:33829595-33829616 | CCCTCCCCCACCTGCTCCCCC | - | 7.16 | | ZNF263 | MA0528.1 | chr1:33829592-33829613 | CTCCCCTCCCCCACCTGCTCC | - | 7.1 |
|
| | Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
| SE_03193 | chr1:33827954-33833250 | Brain_Angular_Gyrus | | SE_03931 | chr1:33826399-33836016 | Brain_Anterior_Caudate | | SE_04902 | chr1:33822310-33834277 | Brain_Cingulate_Gyrus | | SE_05882 | chr1:33826050-33834668 | Brain_Hippocampus_Middle | | SE_06849 | chr1:33827014-33834415 | Brain_Hippocampus_Middle_150 | | SE_07821 | chr1:33822496-33836906 | Brain_Inferior_Temporal_Lobe | | SE_09073 | chr1:33829143-33829607 | Brain_Mid_Frontal_Lobe | | SE_09073 | chr1:33829652-33830555 | Brain_Mid_Frontal_Lobe | | SE_25917 | chr1:33827240-33832198 | Duodenum_Smooth_Muscle | | SE_30304 | chr1:33828568-33832324 | Fetal_Muscle | | SE_33616 | chr1:33827075-33832653 | H2171 | | SE_37317 | chr1:33828525-33832018 | HSMMtube | | SE_40689 | chr1:33826435-33834223 | Left_Ventricle | | SE_42268 | chr1:33828744-33834073 | Lung | | SE_48345 | chr1:33828927-33831644 | Psoas_Muscle | | SE_48801 | chr1:33828750-33834003 | Right_Atrium | | SE_50397 | chr1:33828866-33831857 | Sigmoid_Colon | | SE_51341 | chr1:33826598-33833990 | Skeletal_Muscle | | SE_53534 | chr1:33828984-33831733 | Spleen | | SE_54994 | chr1:33827948-33834036 | Stomach_Smooth_Muscle |
|
| | 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 |
| GH01I033361 | chr1 | 33826803 | 33833802 |
|
Enhancer Sequence | GGAGGGAAAT AGGGTACCCA AGAATCCTGG AATCAGCAAC ACTGCATTGT CCAGCCTATC 60
ACAGACAGAA ATCACTGCCC CCTGCACAAA ACGCTCTCTG TGTTCAAACA AAGCAGCTGT 120
GTGGCCTTCC AGCAGAGTTC TCGCTCCTCA GCTGAGACCT GAGGCGGGCT GAGGATGCAG 180
AACAAAGACC TGGCATCTGG AGGCCCAACT GGGTGAAAGG GCCCTGGCTT TTCAACAACC 240
CGACAGTTCC CTTTTATCAC AGCATATCCC TCCCAGTCAG CAACTTTCTC CTCACCTTTG 300
GGCCTGAGTG TGCACCCAAA GCCTGGAGTT TATCCACTAG AATGAGGACT CCAAGAACCA 360
AGTCTCCTAT CTGGGGCTGT GGCCCACTCC CTTAGGACTC GGCTTCCCTG AAGGCCAGGC 420
CCAAGGGACC CCTGCTGCCT GCCTCTCTTC TGCCCTCCAT TGCTCAGTCC TCATGTCAGT 480
GAGAAGGGCA AGCCAGGCCC TTCTCCTTCC CCTCCAAAGC CCAACCTCTT AGGCTCTGTT 540
CTCCGCCCCT TACTCCCCTC CCCCACCTGC TCCCCCACCC CTATTCTCGG CATAAGGGAC 600
CTTTTCTATT TGCAGAGCCT GAAGAAGCCG GTTGCCAAGG TGACAGGAGC AGGAACAGCA 660
GGGAGCTTGC CATGGGGGAG GGGCTTTGCC CCCAAACAGC TGTCAGTGGG AGCAGTCCCA 720
GCTGGGACTG GAGGGTCTGC CTGCTCTGGG AGGAAACAGC CCCCAGGAGA ACACATTCCT 780
CACTGCCATA CCCCCTCCTA CTGGCCCACT GCAAGTCTCC ACTGGTTACT TTCCCTGGGG 840
GCAGCCAGCC AGCCAGCTCA AAAAATGCTC CAATAACAAA CAAAAAATGT GTGCGCGCTC 900
GCTTGCTTTC TCTCTCCCAG ACACACACAC ACACACACAC ACACTTGCTT TCACACACAC 960
ACACACACAC ACACACACAC ACACACGCTC AAGCACGCTC TTCTCTCCTG CTCTCAGATC 1020
CCTTGGTTCA TTGACAGTGG GTTGGCTGGG CAGGAGGCCA GAAGTCACCT CTGCCCAGGG 1080
AACTGTATAG CCCAAGACAG GTGCTGCTCC TGGCTGCCGT GCACTAGGTC CTAAGAATGA 1140
TTTCAGTCTT TTTGTCCAGA GGCCCTGAGA GGACCTTCCC CTACTAAAAC TCCCCAGCTG 1200
CCTTCCATAT GGGAGGTGGG AGTGGGGCAG CGCCATCTCT GGGCTTACAG AGAGGAAGGG 1260
GTGGGAGAGA GGAAGAATGA ACAGGATGGT GGGAGGCAGG AACAATGCAG GCCCACTGCT 1320
TTGTGTCTCT GGGGAGAGGT TCTTTGTGGA GCTGCAGCTC ACAGCTGCTC CATAGAAAGT 1380
TCTGTGGAGC CACTGGTCTC TGTACTGCAT TCTAGCCAGG CACTGTTAGC CTTAGGCCCT 1440
CGGGCCTCAA GCCTGTCACC TGCTGGTGTT TACCTTTACA TGGGGTCTCC ACCAGACTCT 1500
GCAAACCCTC AATAGGCTTA GACCCCCCAG ATACTTTCAG CTTTGGGTCA GAAACAGGAA 1560
AGGCTGAGGA GGCCCCAGAT TACTGTAAGA ACTGAGAGGG ACGATCTGGC TTGAGATGAA 1620
GAACAGTGTT TGACTCAGCC AGCTATGGCC CCCAGTCCTG CCACTTACTA CTTAGGTGAC 1680
TTTGAGTGCG TGACGGATGT GGTAAGCTCC TGGAGAACCT CTCTGAGCTT CAGTTTGCTC 1740
ATCTGTAAAA TGGATAAAGA CAGCTACCGG ACAGGGATCT TTCCAGGGTT TAAAGAAGCG 1800
TGATGCATAC AATGCAGGGC ACGTTATCTA GCACACGACG GACGTCCTGT GAGTGCTGGT 1860
CCCGTTTCTG TCCAGTTTTC TTGAGAACTG AGTTGCCTAG CAGCCTTAGG AGGAACCCAA 1920
GAACTAGTCT TTCTTTTGAA CAGTGTTAGA ACTTGGGGGG CTGGCTTAGA TTTAGAGAGA 1980
GGTTACATTT CGGCCTGGGC TGGAAGGGGG TTCTCAGGAA GGCCTGAGAC GCAGATGGTC 2040
CGCCAGGGCA TGCGGATTGA ATGAGAAACT AGAAGAAGTG CTCATCTGGG GTCTCAGCTG 2100
TAGTCCAAGC TGCTTTCAAC GCATTGAAAG AGCCCCCAGT CTACCCTTCT GAGCCTCACT 2160
TTCTTTTTCC ATAAAAGGAA GAGGCTGGGC CACTTTCTGG AGAAAGCCAT GCCAGACAGT 2220
GAGAAACATC TGAAGCCACA GGGCCGTGAG GCCTCCGTGG GGAGGTGCCT TTCTTGGCTC 2280
AGCGGTGACC ACTGGAATGC AGCGACTGAC CCTTTGCCCC TGGGTGACTT CTGAAGCCTC 2340
AAGAAGGTGA ATGAGGGATT TTGACCCCGT TTCCTCCTAA CTCAGTGCCA TGTGCGCTGC 2400
TTTGCTTTTC TCTGCCTGGG AACCTTCCCC ACTCTGTCTG TCAGGTCACA TGCTCGTGCC 2460
GCAAGGCTCA TGTGCCATGT CCTCTGAAGG ACGGCATCTC TGACCCATTC TGCCTGACAG 2520
GCAGCTGACC ATCTGTGCCC ACACTGTACC TGGTACTTAG TCCTAAAATA GAATTTATGA 2580
AGTGGAATGG ATTTGCTTCT ATATCTGGTT CCCTTCTTTT GACTGCACAC TCTAGGGAAA 2640
AATAAAAATC CTATCTTATT TTGACAAAGA TGTATTGAGA TATATTCTTG ATGTATTTTC 2700
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