Tag | Content |
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EnhancerAtlas ID | HS010-00271 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr1:144707170-144708370 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HEY2 | MA0649.1 | chr1:144707173-144707183 | GGCACGTGTC | - | 6.02 | IRF1 | MA0050.2 | chr1:144708149-144708170 | AAAAAGAAAGAAAAACTAAGT | - | 6.65 | Npas2 | MA0626.1 | chr1:144707173-144707183 | GGCACGTGTC | + | 6.02 | REST | MA0138.2 | chr1:144707418-144707439 | TTCAGGACCTTGAACAGTGCC | + | 7.67 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_01677 | chr1:144706659-144710717 | Aorta | SE_03221 | chr1:144706788-144710133 | Brain_Angular_Gyrus | SE_04029 | chr1:144706609-144710546 | Brain_Anterior_Caudate | SE_05064 | chr1:144706462-144710582 | Brain_Cingulate_Gyrus | SE_06235 | chr1:144706482-144710790 | Brain_Hippocampus_Middle | SE_07011 | chr1:144706471-144710740 | Brain_Hippocampus_Middle_150 | SE_07990 | chr1:144706462-144710715 | Brain_Inferior_Temporal_Lobe | SE_08841 | chr1:144707216-144710072 | Brain_Mid_Frontal_Lobe | SE_25923 | chr1:144706302-144710597 | Duodenum_Smooth_Muscle | SE_27470 | chr1:144706725-144710210 | Esophagus | SE_29730 | chr1:144706487-144710375 | Fetal_Muscle | SE_35937 | chr1:144706472-144710218 | HMEC | SE_36942 | chr1:144705583-144710527 | HSMMtube | SE_40626 | chr1:144705967-144710848 | Left_Ventricle | SE_42195 | chr1:144705977-144710817 | Lung | SE_45840 | chr1:144706647-144710372 | Osteoblasts | SE_48068 | chr1:144705887-144710814 | Psoas_Muscle | SE_48631 | chr1:144706700-144710723 | Right_Atrium | SE_49499 | chr1:144706934-144708407 | Right_Ventricle | SE_51075 | chr1:144705416-144710930 | Skeletal_Muscle | SE_51843 | chr1:144706536-144710128 | Skeletal_Muscle_Myoblast | SE_54600 | chr1:144706061-144710921 | Stomach_Smooth_Muscle | SE_63621 | chr1:144706648-144710142 | HSMM | SE_65234 | chr1:144706812-144710151 | NHEK |
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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 |
GH01I120287 | chr1 | 144706689 | 144709914 |
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Enhancer Sequence | AGGGGCACGT GTCCTCAACC TTGGCAAAAT AAACTTTCTA AATTTACTGA GACCTGTCTC 60 AAATTTTCGG AGTTCACAGT GGGCAAGACT AGATTTACTT TTGTGTTGAG CAGATACTGA 120 GCTTGACTGA TAAGAATCTG GAGTGTGAGG TCTCACGGAG TAACTCTGAT AGAGGAAGCT 180 ACCTGTGTGG TCTCAGGGAG AAGATCTGAG ACTTACCAAG AAAAAGTGAC CTGAAAGAAC 240 TGGCTGACTT CAGGACCTTG AACAGTGCCT AGACCCTCTT TCTGCAGCTC CAGATCATAG 300 CCATCATGCT GGCAGCCTCC CTGCCGCTCA TCCAGGCACC TTAAAGAAGG GCTTCCTCTT 360 CCCAAGCCTC TGGGTGGGCT TTCTAAAGCC CTGTGTGCAT GAAGAGGTGG CTTGTAGCCC 420 TTTGCAGCAG CAGGGCTTAC ATGAGGCTGG GATATGAAAA GCTGGCATTA CAATGCAGCT 480 TGTGCCTTGC ATTCACTCCC CACTTCATCA AGCCAAGTTT CTAAATAACA GGGATAGTAA 540 CTGCCCACTG TGGCCCAATG TCACTTCTAA AGTTGCTTGG CAAAAAGCCA CATGACTATT 600 ACTTAGCTCT CCACAGAACG GCATGTACCA AGTCGGATCA CTGCTGTCGG TGTGTGGGTG 660 GATTAGCTGC TATTGAACAT GATAGGGCGG GCCCCTTTCC AGTTTGCACC AGCCCCGCTC 720 TGTGCCTACT CCATGTATCA TAGAGCCTCC TCTCTCTGTG CAGTTGAACT TGATCAGATG 780 AGATGGCAAG AGCCAGAGCA GGGAGCAAGG CAAAAGAGAA AAATATGTTC ACGGTGACTT 840 TTGAAAACAT ATGGATGAAA CTCCTGAGGA GGCTGAGGAA CTAAACCTTT TCTTTTGGCA 900 GTAGGCACAG AGTGCAGATT CATCTCTCTG TAATTACTCT AGCTCCTGCT GTGTGAGTTC 960 TATTTTAGCC CAGTAATGCA AAAAGAAAGA AAAACTAAGT TCTGACAAGC ACTTACATTT 1020 CTTGAATTTT TGTTGAAGGT CCCAGAGGTC ATTGTAAGCA GCCTGAACAG GTAGTTAGGG 1080 CTCCTGGATT CTAGTCTCAG CTTGGCTACT AATTTACCGT GTGACGTTAG GCAAATTACT 1140 ATTCTGAGCT TTAGTCATCT TATCTTTAAA ATGAAGGGTT TATTCTTTAG AGGAAGCTGA 1200
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