Tag | Content |
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EnhancerAtlas ID | HS180-10568 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr12:6330920-6332610 |
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: 2 | Chromosome | Start | End |
chr12 | 6330976 | 6331800 | chr12 | 6332055 | 6332244 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I006213 | chr12 | 6322280 | 6345639 |
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Enhancer Sequence | TGCTTGAGGC CAGGAATTTA AGACCAGCCT GAGCAACATA GCGAGACCCC TGGCTCTACA 60 AAAAAAAAAA AAAAAAAAAG GGTTTAAAAT ATTAGCCAGG ATTAGCGGCA TGCACCTGTA 120 ATCCCAGCTA CTCAGGAGGC TGAGGTGGAA GAATGGCTTG AGCCCAGGAG TCCAAGGCTA 180 CAGTGAGCTA TGATTGCACC ACTGCACTCC AGCCTGGGTG ACGAGAGCAA GACCCTGTCT 240 CAAAAAATAA AGCAGCTGGG GTGAAAGCCG GATGGGGACA GGGGAGCCCC TCTATGCCAC 300 ACCAGAAAGT GAGTTCTCCT AGAAAATACT TCAGAGCGCC TTAGATAGCG CTGCCTGACA 360 ACCATGAAAG GCATTATTGG GTGGCACTGG TTATACAAGT TTTGTGACCC TGTGACCCCA 420 AGCCATTGTG ACTCAGCCAA CTGGAGCAAT GTCTCCAACA GCGTTACAGA AAATGGGGCA 480 GCTGATGGTT CACATAGCAT CCCCCCCGGC CGGTGAACTC AGTCATTCTG TCAGAAAAGG 540 CAGCAGGGTT CACTCCTGAT TTTTGTCCAA GTGTTCCCAG TCATGCCCCT GGCCCTCCCT 600 TTTCTCTGGG TTACTTGAAC CTTTCTCCTC TCTTATTGTG AGTTGTTAAG CCTGTGAGAC 660 CGAGACCTAT GGCAGCTTTT CCCATTTCTC CAGAGCCAGC TGCTTTTCCT TCCTGGTTGT 720 AGTGAAATGT TGTAGCTTTG ACAACCAAGC CGCATGATGT AAGGTTTAAG GTGGGGTCCG 780 AATGCGGGGG ACTCCCGACT CCGGGCTTGG CCTGGCCCTT GGCCAAGATA AGAGACCTGA 840 GATGCTTCCT TTTCCCTCGT GGTTCCAGTT CTCCAGCCCA GCATCCTTCT TACCACCTGT 900 GCACAGAGAC CGGATCAATG ACTGGACTTA ACATATTGGC TCAGGGTCCT CGACATTGGG 960 GCTCTCTATA AGATGGAAGG GGCCTTACCC CTGGAGGTTC CACTGGGGTA CCCTGTCATT 1020 ATCTGAGCGT GGAACATTCC CAGAGAGACG CAGCTCCTGC TCGTGAGAGG CTGCTGTGCA 1080 GAGCGTAGCT TTACCTCATC TTACAGCTTA GTTCCTTGGC AGACCTGGGA TTGTTTTCGT 1140 TCTTTTCTGC GACTCAGTTT TCCCAGCAGA TAAGGGGTGG GGTCATAACT TCACTCATCA 1200 GGGGAAGTAA GATGACTTGG GAGATAATTG CTTGATAAGC ACAAGCCTAG AGCAAAAAGG 1260 ACAGTAATGA GCACTGTCTC GCTATCTCCC TATGCGCGCA AGAGCATCAC AAGACCAGGG 1320 CGAGAGGGAG GACCAGGGTG AGAAACAGGT TGTGGCTAAA CGTGGACCAA AATTGAGCAC 1380 CGGCCTACAG TTTTCAGGTT AACGCTTTTA TGTCCAGGAG GCCAGCAGCT TCAGTCTTCC 1440 ATTCCCAGGG GACTGACTGG GCCTCCCTGG GGTTGGGGTG GAAGGAGGGA AGGTATCACC 1500 TTTGTACTTT TTTTTTTTTT TTTTTGAGAG GGAGTCTCGC TCTGTCGCCC AGGCTGGAGT 1560 GCAGTGGCGC AATCTCCGCT CACTGCAAGC TCCGCCTCCC GGGCTCACGC CATTCTCCTG 1620 CCTCAGCCTC TGGAGTAGCT GGGACTACAG GCGCCCGCCA CCACGCCTGG AGAATTTTTT 1680 GTATTTTTAG 1690
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