Tag | Content |
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EnhancerAtlas ID | HS116-07789 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr12:6331080-6332430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr12:6332360-6332374 | ATTCCCAGGGGACT | - | 6.59 | EBF1 | MA0154.3 | chr12:6332360-6332374 | ATTCCCAGGGGACT | + | 6.74 | EWSR1-FLI1 | MA0149.1 | chr12:6332399-6332417 | GGAAGGAGGGAAGGTATC | + | 6.45 | EWSR1-FLI1 | MA0149.1 | chr12:6332395-6332413 | GGGTGGAAGGAGGGAAGG | + | 6.56 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_01613 | chr12:6331068-6332334 | Aorta | SE_03308 | chr12:6331173-6332411 | Brain_Angular_Gyrus | SE_03988 | chr12:6328807-6336415 | Brain_Anterior_Caudate | SE_04905 | chr12:6328630-6346354 | Brain_Cingulate_Gyrus | SE_05857 | chr12:6328573-6346408 | Brain_Hippocampus_Middle | SE_06790 | chr12:6328750-6346091 | Brain_Hippocampus_Middle_150 | SE_07876 | chr12:6328735-6347463 | Brain_Inferior_Temporal_Lobe | SE_08879 | chr12:6331617-6331845 | Brain_Mid_Frontal_Lobe | SE_08879 | chr12:6331934-6332225 | Brain_Mid_Frontal_Lobe | SE_23086 | chr12:6330958-6332424 | Colon_Crypt_1 | SE_23760 | chr12:6331109-6332358 | Colon_Crypt_2 | SE_24754 | chr12:6331065-6332427 | Colon_Crypt_3 | SE_25881 | chr12:6331138-6332492 | Duodenum_Smooth_Muscle | SE_26531 | chr12:6328841-6332525 | Esophagus | SE_27879 | chr12:6330794-6343416 | Fetal_Intestine | SE_28805 | chr12:6330455-6345849 | Fetal_Intestine_Large | SE_31631 | chr12:6330908-6332515 | Gastric | SE_33937 | chr12:6330804-6332438 | HCC1954 | SE_35850 | chr12:6331075-6332437 | HMEC | SE_37940 | chr12:6328841-6332447 | HUVEC | SE_41591 | chr12:6331083-6332422 | LNCaP | SE_42122 | chr12:6328842-6332515 | Lung | SE_48662 | chr12:6331176-6332445 | Right_Atrium | SE_50072 | chr12:6330980-6332462 | Sigmoid_Colon | SE_52457 | chr12:6330890-6332501 | Small_Intestine | SE_54512 | chr12:6320070-6346293 | Stomach_Smooth_Muscle | SE_57134 | chr12:6331268-6332449 | VACO_400 | SE_57526 | chr12:6331004-6332437 | VACO_503 | SE_57940 | chr12:6331422-6332473 | VACO_9m | SE_64246 | chr12:6331037-6332392 | 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 |
GH12I006213 | chr12 | 6322280 | 6345639 |
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Enhancer Sequence | AGCCCAGGAG TCCAAGGCTA CAGTGAGCTA TGATTGCACC ACTGCACTCC AGCCTGGGTG 60 ACGAGAGCAA GACCCTGTCT CAAAAAATAA AGCAGCTGGG GTGAAAGCCG GATGGGGACA 120 GGGGAGCCCC TCTATGCCAC ACCAGAAAGT GAGTTCTCCT AGAAAATACT TCAGAGCGCC 180 TTAGATAGCG CTGCCTGACA ACCATGAAAG GCATTATTGG GTGGCACTGG TTATACAAGT 240 TTTGTGACCC TGTGACCCCA AGCCATTGTG ACTCAGCCAA CTGGAGCAAT GTCTCCAACA 300 GCGTTACAGA AAATGGGGCA GCTGATGGTT CACATAGCAT CCCCCCCGGC CGGTGAACTC 360 AGTCATTCTG TCAGAAAAGG CAGCAGGGTT CACTCCTGAT TTTTGTCCAA GTGTTCCCAG 420 TCATGCCCCT GGCCCTCCCT TTTCTCTGGG TTACTTGAAC CTTTCTCCTC TCTTATTGTG 480 AGTTGTTAAG CCTGTGAGAC CGAGACCTAT GGCAGCTTTT CCCATTTCTC CAGAGCCAGC 540 TGCTTTTCCT TCCTGGTTGT AGTGAAATGT TGTAGCTTTG ACAACCAAGC CGCATGATGT 600 AAGGTTTAAG GTGGGGTCCG AATGCGGGGG ACTCCCGACT CCGGGCTTGG CCTGGCCCTT 660 GGCCAAGATA AGAGACCTGA GATGCTTCCT TTTCCCTCGT GGTTCCAGTT CTCCAGCCCA 720 GCATCCTTCT TACCACCTGT GCACAGAGAC CGGATCAATG ACTGGACTTA ACATATTGGC 780 TCAGGGTCCT CGACATTGGG GCTCTCTATA AGATGGAAGG GGCCTTACCC CTGGAGGTTC 840 CACTGGGGTA CCCTGTCATT ATCTGAGCGT GGAACATTCC CAGAGAGACG CAGCTCCTGC 900 TCGTGAGAGG CTGCTGTGCA GAGCGTAGCT TTACCTCATC TTACAGCTTA GTTCCTTGGC 960 AGACCTGGGA TTGTTTTCGT TCTTTTCTGC GACTCAGTTT TCCCAGCAGA TAAGGGGTGG 1020 GGTCATAACT TCACTCATCA GGGGAAGTAA GATGACTTGG GAGATAATTG CTTGATAAGC 1080 ACAAGCCTAG AGCAAAAAGG ACAGTAATGA GCACTGTCTC GCTATCTCCC TATGCGCGCA 1140 AGAGCATCAC AAGACCAGGG CGAGAGGGAG GACCAGGGTG AGAAACAGGT TGTGGCTAAA 1200 CGTGGACCAA AATTGAGCAC CGGCCTACAG TTTTCAGGTT AACGCTTTTA TGTCCAGGAG 1260 GCCAGCAGCT TCAGTCTTCC ATTCCCAGGG GACTGACTGG GCCTCCCTGG GGTTGGGGTG 1320 GAAGGAGGGA AGGTATCACC TTTGTACTTT 1350
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