Tag | Content |
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EnhancerAtlas ID | HS105-33225 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr17:16913210-16914820 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr17:16914069-16914080 | GGTGACTCATG | + | 6.62 | FOSL2 | MA0478.1 | chr17:16914068-16914079 | GGGTGACTCAT | + | 6.14 | JUN(var.2) | MA0489.1 | chr17:16914065-16914079 | GAGGGGTGACTCAT | + | 6.1 | JUNB | MA0490.1 | chr17:16914068-16914079 | GGGTGACTCAT | + | 6.32 | JUND | MA0491.1 | chr17:16914069-16914080 | GGTGACTCATG | + | 6.02 | ZIC3 | MA0697.1 | chr17:16913511-16913526 | GCTCAGCAGGGGGTT | - | 6.12 | ZNF263 | MA0528.1 | chr17:16914367-16914388 | TGAGGAGGGCGAGCAGGAAGG | + | 6.84 | ZNF263 | MA0528.1 | chr17:16914690-16914711 | CTCCCACCCCTTCCGTCCTCC | - | 6 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_03884 | chr17:16913012-16915519 | Brain_Anterior_Caudate | SE_04928 | chr17:16912965-16915433 | Brain_Cingulate_Gyrus | SE_05858 | chr17:16910885-16915644 | Brain_Hippocampus_Middle | SE_23636 | chr17:16913280-16915489 | Colon_Crypt_1 | SE_24609 | chr17:16913349-16915236 | Colon_Crypt_2 | SE_26997 | chr17:16913232-16915454 | Esophagus | SE_27670 | chr17:16913014-16915514 | Fetal_Intestine | SE_28856 | chr17:16912988-16915594 | Fetal_Intestine_Large | SE_31426 | chr17:16911294-16915533 | Gastric | SE_34197 | chr17:16913015-16915492 | HCC1954 | SE_34341 | chr17:16910923-16915870 | HCT-116 | SE_34638 | chr17:16911053-16916556 | HeLa | SE_35971 | chr17:16912952-16915524 | HMEC | SE_37027 | chr17:16912540-16915700 | HSMMtube | SE_41253 | chr17:16913151-16915400 | Left_Ventricle | SE_42192 | chr17:16913006-16915550 | Lung | SE_46284 | chr17:16912929-16915506 | Osteoblasts | SE_47491 | chr17:16913333-16915163 | Pancreas | SE_52055 | chr17:16913231-16915357 | Skeletal_Muscle_Myoblast | SE_55953 | chr17:16912112-16915638 | u87 | SE_57371 | chr17:16913179-16914126 | VACO_503 | SE_57371 | chr17:16914183-16915422 | VACO_503 | SE_58168 | chr17:16913504-16914813 | VACO_9m | SE_63843 | chr17:16913199-16915461 | HSMM | SE_65457 | chr17:16912950-16915516 | Pancreatic_islets |
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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 |
GH17I017009 | chr17 | 16913262 | 16915113 |
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Enhancer Sequence | TCTAACTTGT TGCATGGAAG AGTCATTTGG TCTTTTCCTC TGCTATGCAA TGCAGGAGAA 60 CATTTGTTTG TTTTTAGTTT ATAGAATGCA GTAAGTTTTC TTTTGGTGGA CATCAGCACT 120 TGTTTCTCTT GGGTGTCTGA CCCTTTCCCA TGCTTTCCAA CCCTAGCTTC TAAGCTCTCT 180 GAGGGTACAG AGTTTGCCTC TGTCTATCCT GGCCTGACAC GCAGTCTCCT CCTGTCAGCA 240 TTTACTCAGT CCAAATTGCA ACAGGGGCAG GTCCCTGCCA GCTGAGGGAG CTATTCTTCC 300 AGCTCAGCAG GGGGTTGGCC AGTCTTGTCC TCTGGGACAA AGCCCAGCCA GAGTTCTGGG 360 CACTGTGGTT CAGAAGGCCT GAGACACGTG GTTTTACCAG GGCTGGGTAC CAAGAACCAT 420 GCTTGAGGCT GACGGCATTT CATTGGCAGC GTCTGTGGGG GGCTTGGGGA CTCAGCCGTG 480 GGAAGCCTGT TCTGCACACA GCCATGGCGC AAGAAATGCT TTTTCCTGCG ACGGTTCAGT 540 GAGAACCATG ATGGCAGTGG TGCAGCATCC TCCCAGCTTG GTTTTTAAAC ATGGGAAGGG 600 CTTCTAAAAA GTCACACAGC TGGTTAATGT TTGAACCAGG GTGGCACAGG TTTGTGCGAA 660 GCAGTGAGTG GAGCTGTCTG AATGCCAGGA GGAGGGTCAC CCTGGAGGCG GGTGACACAG 720 GGGTCAGTGC AGGTCAGAGG CAGAGGCTGG GCCCAGATGC CATGCGAGCT CCAGGCCACT 780 TTCCCAGAGA AGTGAGCGGC GGCCAGGCTG CCGGAGGCTG TGTGGCCTCT TCAGGCCCTC 840 ACTGGTCCTG ATTTTGAGGG GTGACTCATG CCGGCTTGGA CATCCACTTC TGGCTCAAGT 900 TGCTCTGGGT TCCTCCACAC AGACCAGAGG GATTCCTGCG TCACAGGAAT CCAGGAAGGG 960 GTGGGGGGAG TTGCAGGTTG AGAAGACAGA GGTGAGTGGC CCCCGGGCCC CTCCCCTGTT 1020 GAGTCACGGG AAGGGAATGG AAATAGTGTG TGCTGAAGCT GAGTCAGGGC CCAGCCTCAC 1080 CTTCTCGGGA CCTCATATGG GCTCTGAGGC GAGAGGCCCA CCTGTCCCCC CCTCCTTGCT 1140 GCCTCCTCTC CCAAGCATGA GGAGGGCGAG CAGGAAGGAT TTAGGTTAGC TCTCAAGAAG 1200 GACTTCCTGA ATCGCGCCAG GCGACACTGA GAGGCATCTC TCAAAGGAAG TTGTGAAATC 1260 TTCCTTGGGA CCAATTTGAG GTTTGGTCTG GGTCCAACCA GGACTATCTT TATGGCTCTA 1320 GAATATTTTC AAGTGTTAGA CATTCCTTCC TCGACATGAC TCAGGGAGCA TCCGATGTGT 1380 GCCAGGCCTG GTGGCAGGAG CAGGGCCAGC TGAGTGTGGG ACATGCCCCA CTCTGGGGGT 1440 CTTCTCTAGG TCAGCATTAC AGCAGCCTTG GAGAAGACGG CTCCCACCCC TTCCGTCCTC 1500 CCCTCTCCTG GCTCCCTTGG GCAGCCTGCT CTGCCAGCCA CACCACACTC CACTTTCGGA 1560 TTCCGGAAGG AAACTATGGG TAATAAATAG GACAAAGGGT CAATTTCCTT 1610
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