Tag | Content |
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EnhancerAtlas ID | HS064-08216 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr2:55360440-55361860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr2:55361572-55361587 | CAGGTCCAAAGTCCA | + | 6.67 | MSC | MA0665.1 | chr2:55361713-55361723 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr2:55361713-55361723 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr2:55361713-55361723 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr2:55361713-55361723 | AACAGCTGTT | - | 6.02 | RELA | MA0107.1 | chr2:55361168-55361178 | GGGAATTTCC | + | 6.02 | SRF | MA0083.3 | chr2:55361203-55361219 | AGACCATATATGGTAA | + | 7.54 | SRF | MA0083.3 | chr2:55361203-55361219 | AGACCATATATGGTAA | - | 7.72 | STAT1 | MA0137.3 | chr2:55361151-55361162 | TTTCTGGGAAA | + | 6.02 | STAT3 | MA0144.2 | chr2:55361151-55361162 | TTTCTGGGAAA | + | 6.32 | Stat4 | MA0518.1 | chr2:55361151-55361165 | TTTCTGGGAAAGGG | + | 6.56 | ZNF263 | MA0528.1 | chr2:55361455-55361476 | CCCTCTTCCCCCCACTCCTCC | - | 8.16 |
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| Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
SE_00239 | chr2:55360036-55362701 | Adipose_Nuclei | SE_03190 | chr2:55360357-55361196 | Brain_Angular_Gyrus | SE_03190 | chr2:55361211-55362296 | Brain_Angular_Gyrus | SE_03921 | chr2:55360184-55362316 | Brain_Anterior_Caudate | SE_04845 | chr2:55360042-55370718 | Brain_Cingulate_Gyrus | SE_05873 | chr2:55360067-55370846 | Brain_Hippocampus_Middle | SE_06720 | chr2:55360082-55370702 | Brain_Hippocampus_Middle_150 | SE_07801 | chr2:55360052-55362334 | Brain_Inferior_Temporal_Lobe | SE_08941 | chr2:55360580-55360981 | Brain_Mid_Frontal_Lobe | SE_08941 | chr2:55361418-55361579 | Brain_Mid_Frontal_Lobe | SE_13769 | chr2:55360062-55362262 | CD34_Primary_RO01536 | SE_14856 | chr2:55360330-55362562 | CD4_Memory_Primary_7pool | SE_21142 | chr2:55360073-55362248 | CD8_Memory_7pool | SE_27564 | chr2:55360421-55362286 | Esophagus | SE_37014 | chr2:55360373-55361714 | HSMMtube | SE_39897 | chr2:55360383-55362291 | K562 | SE_43033 | chr2:55360367-55362254 | Lung | SE_45296 | chr2:55360375-55362106 | NHLF | SE_46551 | chr2:55360253-55362216 | Osteoblasts | SE_49902 | chr2:55360326-55362325 | RPMI-8402 | SE_54907 | chr2:55360260-55362167 | Stomach_Smooth_Muscle | SE_56652 | chr2:55360310-55361998 | u87 |
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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 |
GH02I055133 | chr2 | 55360223 | 55362349 |
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Enhancer Sequence | GTGAAATAAG CACATCATGG AGAATGCGGT GTTGTCTTTT GCTTGTTTAC TTTTTATTTT 60 TCAGTTTATT TGTTCCCTCT CCCTGCCTTT TTTTTACTTG CAAAAGCAAT AAATACTTGT 120 AAAAATTGTC AGAAAGGTAT AAATCTACTT CCCAATAATA CGGGAGGACT GTGTCATGTG 180 TATTTCTTGT AACCTCCTCC TTATGCAGGA TACTGCCCAC ACCGGTATGT GTTCAGTTCA 240 ATTCCGTTAG AACTACTGTT CCTCACAAGG CTGTAAGGTA CCCTTGAGGT GTCTAGTCCA 300 ATTCCTCCAT TCTATGGAGG GAGAAACTGA GGCCCTGAGA AGAAGGGAAA CTTAGTTAGG 360 GACCCTGAGC TGGTTAAGTG ACAGAACCAT AAATAGCTCT CACCGTCCTT AACATAGCCC 420 CTGCCAGATA ACCCCTAAGG AGACCCAGCA GCCACACGGC TGATAAAGCC ACTGCTTGTC 480 AAGATGTCAC AGGGTGAACC CCAAAATTGG GGTTCAGCCC AGGAAGTCAT GTGGGTTCTT 540 GGCTCCAAAC AGGAAGAGCG AGCCAAGAGA GCAAAGTGAA AGCAAGTTTA TTAAGTAAAG 600 GAATGAAAGG GTGGAGAGTC CACAGGCAAA GCAACCCCAA AGGCTGCTGG TTGGCTATTT 660 TGATGGTGAT TTCTTAATCA CATGCTAAAC AAAGAGTGGA TTTTCATGAG CTTTCTGGGA 720 AAGGGGTGGG GAATTTCCAC AACTGAGGGT TCCTCTCCCT TTCAGACCAT ATATGGTAAC 780 TTCCAGACGG TTGCCATGGC TTTTGTAAAC TGTCATGTCG CTAGTGGGCA TTTCCTTTAG 840 TATGCTAATT TATTATAATT AGTGTATAAC GAGCAGAGAG GACAACCAGA GATTGCTTTT 900 GTGGTCACGT GGGTTTTGAT TGATTTTCAC TTGCCTCTTT ACCGCATCCT GTTTTATCTG 960 TGGGGTCTTT ATGATTTGTA TCTTGTGAAC TCCTATCTCA CTACCATCAG CATTCCCCTC 1020 TTCCCCCCAC TCCTCCTGAC CTCTTGACAG AAGCTGAGGA AATGGGAAAG CAGATCCTAG 1080 ACTTGGAGAA GGTCTGTGTG GGGTCCAAGG CCACTCAGTA ATAAGACTCC CCCAGGTCCA 1140 AAGTCCAGAG ACAGCCCCCA GACTCACTCC ATCTCTCAGA GGCTGATGCC CACCCAGCAG 1200 GCATTCACCT TAGCTCAGAG CAGCACCAAT TTCCTGCATG CAGTCAATAA AGTGCAGTTT 1260 GCTTCCTGAC ATAAACAGCT GTTCTCAGAA AGCAAATATG CAAAGAGAAT ATTATTCTTC 1320 AAGTTTAAAT GAGGAAGAAG AAAGGGTGGG TGAAGCGGGA GGTGGGAGCT TACACAGAGT 1380 TCTAGGTTTA TAATCTAATT CTCCAGAGCC AGCCTCTGAC 1420
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