| Tag | Content |
|---|
EnhancerAtlas ID | HS078-00694 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr1:33828850-33831690 |
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 | ATGATTGTGG ATTTTTCTCC TAACATAAAA AGAGATTCTT AGTCATCTAG ATTTGGTGCT 60
ACAGTGGATA GCTGAAATGA CCTTCATCAA AATCGTTGGG GATTTTAGCA GATGACAGTC 120
CCACCTGTAT GCTTTGGTTT TTATTGGATT CCCTAAGTAA AAGTGTGCTT GCAGTTTGGA 180
GGCTGCTTTG GGAGGGAAAT AGGGTACCCA AGAATCCTGG AATCAGCAAC ACTGCATTGT 240
CCAGCCTATC ACAGACAGAA ATCACTGCCC CCTGCACAAA ACGCTCTCTG TGTTCAAACA 300
AAGCAGCTGT GTGGCCTTCC AGCAGAGTTC TCGCTCCTCA GCTGAGACCT GAGGCGGGCT 360
GAGGATGCAG AACAAAGACC TGGCATCTGG AGGCCCAACT GGGTGAAAGG GCCCTGGCTT 420
TTCAACAACC CGACAGTTCC CTTTTATCAC AGCATATCCC TCCCAGTCAG CAACTTTCTC 480
CTCACCTTTG GGCCTGAGTG TGCACCCAAA GCCTGGAGTT TATCCACTAG AATGAGGACT 540
CCAAGAACCA AGTCTCCTAT CTGGGGCTGT GGCCCACTCC CTTAGGACTC GGCTTCCCTG 600
AAGGCCAGGC CCAAGGGACC CCTGCTGCCT GCCTCTCTTC TGCCCTCCAT TGCTCAGTCC 660
TCATGTCAGT GAGAAGGGCA AGCCAGGCCC TTCTCCTTCC CCTCCAAAGC CCAACCTCTT 720
AGGCTCTGTT CTCCGCCCCT TACTCCCCTC CCCCACCTGC TCCCCCACCC CTATTCTCGG 780
CATAAGGGAC CTTTTCTATT TGCAGAGCCT GAAGAAGCCG GTTGCCAAGG TGACAGGAGC 840
AGGAACAGCA GGGAGCTTGC CATGGGGGAG GGGCTTTGCC CCCAAACAGC TGTCAGTGGG 900
AGCAGTCCCA GCTGGGACTG GAGGGTCTGC CTGCTCTGGG AGGAAACAGC CCCCAGGAGA 960
ACACATTCCT CACTGCCATA CCCCCTCCTA CTGGCCCACT GCAAGTCTCC ACTGGTTACT 1020
TTCCCTGGGG GCAGCCAGCC AGCCAGCTCA AAAAATGCTC CAATAACAAA CAAAAAATGT 1080
GTGCGCGCTC GCTTGCTTTC TCTCTCCCAG ACACACACAC ACACACACAC ACACTTGCTT 1140
TCACACACAC ACACACACAC ACACACACAC ACACACGCTC AAGCACGCTC TTCTCTCCTG 1200
CTCTCAGATC CCTTGGTTCA TTGACAGTGG GTTGGCTGGG CAGGAGGCCA GAAGTCACCT 1260
CTGCCCAGGG AACTGTATAG CCCAAGACAG GTGCTGCTCC TGGCTGCCGT GCACTAGGTC 1320
CTAAGAATGA TTTCAGTCTT TTTGTCCAGA GGCCCTGAGA GGACCTTCCC CTACTAAAAC 1380
TCCCCAGCTG CCTTCCATAT GGGAGGTGGG AGTGGGGCAG CGCCATCTCT GGGCTTACAG 1440
AGAGGAAGGG GTGGGAGAGA GGAAGAATGA ACAGGATGGT GGGAGGCAGG AACAATGCAG 1500
GCCCACTGCT TTGTGTCTCT GGGGAGAGGT TCTTTGTGGA GCTGCAGCTC ACAGCTGCTC 1560
CATAGAAAGT TCTGTGGAGC CACTGGTCTC TGTACTGCAT TCTAGCCAGG CACTGTTAGC 1620
CTTAGGCCCT CGGGCCTCAA GCCTGTCACC TGCTGGTGTT TACCTTTACA TGGGGTCTCC 1680
ACCAGACTCT GCAAACCCTC AATAGGCTTA GACCCCCCAG ATACTTTCAG CTTTGGGTCA 1740
GAAACAGGAA AGGCTGAGGA GGCCCCAGAT TACTGTAAGA ACTGAGAGGG ACGATCTGGC 1800
TTGAGATGAA GAACAGTGTT TGACTCAGCC AGCTATGGCC CCCAGTCCTG CCACTTACTA 1860
CTTAGGTGAC TTTGAGTGCG TGACGGATGT GGTAAGCTCC TGGAGAACCT CTCTGAGCTT 1920
CAGTTTGCTC ATCTGTAAAA TGGATAAAGA CAGCTACCGG ACAGGGATCT TTCCAGGGTT 1980
TAAAGAAGCG TGATGCATAC AATGCAGGGC ACGTTATCTA GCACACGACG GACGTCCTGT 2040
GAGTGCTGGT CCCGTTTCTG TCCAGTTTTC TTGAGAACTG AGTTGCCTAG CAGCCTTAGG 2100
AGGAACCCAA GAACTAGTCT TTCTTTTGAA CAGTGTTAGA ACTTGGGGGG CTGGCTTAGA 2160
TTTAGAGAGA GGTTACATTT CGGCCTGGGC TGGAAGGGGG TTCTCAGGAA GGCCTGAGAC 2220
GCAGATGGTC CGCCAGGGCA TGCGGATTGA ATGAGAAACT AGAAGAAGTG CTCATCTGGG 2280
GTCTCAGCTG TAGTCCAAGC TGCTTTCAAC GCATTGAAAG AGCCCCCAGT CTACCCTTCT 2340
GAGCCTCACT TTCTTTTTCC ATAAAAGGAA GAGGCTGGGC CACTTTCTGG AGAAAGCCAT 2400
GCCAGACAGT GAGAAACATC TGAAGCCACA GGGCCGTGAG GCCTCCGTGG GGAGGTGCCT 2460
TTCTTGGCTC AGCGGTGACC ACTGGAATGC AGCGACTGAC CCTTTGCCCC TGGGTGACTT 2520
CTGAAGCCTC AAGAAGGTGA ATGAGGGATT TTGACCCCGT TTCCTCCTAA CTCAGTGCCA 2580
TGTGCGCTGC TTTGCTTTTC TCTGCCTGGG AACCTTCCCC ACTCTGTCTG TCAGGTCACA 2640
TGCTCGTGCC GCAAGGCTCA TGTGCCATGT CCTCTGAAGG ACGGCATCTC TGACCCATTC 2700
TGCCTGACAG GCAGCTGACC ATCTGTGCCC ACACTGTACC TGGTACTTAG TCCTAAAATA 2760
GAATTTATGA AGTGGAATGG ATTTGCTTCT ATATCTGGTT CCCTTCTTTT GACTGCACAC 2820
TCTAGGGAAA AATAAAAATC 2840
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