Tag | Content |
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EnhancerAtlas ID | HS104-24881 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr17:16913080-16915310 |
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: 26 | 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_58168 | chr17:16914820-16915158 | 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 | CCTCAGCCTC CCAAAGTGTT GGGACTACAG GCGTGAGCCA CCGCACCCAA CCTTGCCTGT 60 TTTTGACCTC CATACTGTGC ATGCTCTTTT GCGTCTGGAT TCTTTTGTCT GACTTTATCT 120 GCGAGATTCA TCTAACTTGT TGCATGGAAG AGTCATTTGG TCTTTTCCTC TGCTATGCAA 180 TGCAGGAGAA CATTTGTTTG TTTTTAGTTT ATAGAATGCA GTAAGTTTTC TTTTGGTGGA 240 CATCAGCACT TGTTTCTCTT GGGTGTCTGA CCCTTTCCCA TGCTTTCCAA CCCTAGCTTC 300 TAAGCTCTCT GAGGGTACAG AGTTTGCCTC TGTCTATCCT GGCCTGACAC GCAGTCTCCT 360 CCTGTCAGCA TTTACTCAGT CCAAATTGCA ACAGGGGCAG GTCCCTGCCA GCTGAGGGAG 420 CTATTCTTCC AGCTCAGCAG GGGGTTGGCC AGTCTTGTCC TCTGGGACAA AGCCCAGCCA 480 GAGTTCTGGG CACTGTGGTT CAGAAGGCCT GAGACACGTG GTTTTACCAG GGCTGGGTAC 540 CAAGAACCAT GCTTGAGGCT GACGGCATTT CATTGGCAGC GTCTGTGGGG GGCTTGGGGA 600 CTCAGCCGTG GGAAGCCTGT TCTGCACACA GCCATGGCGC AAGAAATGCT TTTTCCTGCG 660 ACGGTTCAGT GAGAACCATG ATGGCAGTGG TGCAGCATCC TCCCAGCTTG GTTTTTAAAC 720 ATGGGAAGGG CTTCTAAAAA GTCACACAGC TGGTTAATGT TTGAACCAGG GTGGCACAGG 780 TTTGTGCGAA GCAGTGAGTG GAGCTGTCTG AATGCCAGGA GGAGGGTCAC CCTGGAGGCG 840 GGTGACACAG GGGTCAGTGC AGGTCAGAGG CAGAGGCTGG GCCCAGATGC CATGCGAGCT 900 CCAGGCCACT TTCCCAGAGA AGTGAGCGGC GGCCAGGCTG CCGGAGGCTG TGTGGCCTCT 960 TCAGGCCCTC ACTGGTCCTG ATTTTGAGGG GTGACTCATG CCGGCTTGGA CATCCACTTC 1020 TGGCTCAAGT TGCTCTGGGT TCCTCCACAC AGACCAGAGG GATTCCTGCG TCACAGGAAT 1080 CCAGGAAGGG GTGGGGGGAG TTGCAGGTTG AGAAGACAGA GGTGAGTGGC CCCCGGGCCC 1140 CTCCCCTGTT GAGTCACGGG AAGGGAATGG AAATAGTGTG TGCTGAAGCT GAGTCAGGGC 1200 CCAGCCTCAC CTTCTCGGGA CCTCATATGG GCTCTGAGGC GAGAGGCCCA CCTGTCCCCC 1260 CCTCCTTGCT GCCTCCTCTC CCAAGCATGA GGAGGGCGAG CAGGAAGGAT TTAGGTTAGC 1320 TCTCAAGAAG GACTTCCTGA ATCGCGCCAG GCGACACTGA GAGGCATCTC TCAAAGGAAG 1380 TTGTGAAATC TTCCTTGGGA CCAATTTGAG GTTTGGTCTG GGTCCAACCA GGACTATCTT 1440 TATGGCTCTA GAATATTTTC AAGTGTTAGA CATTCCTTCC TCGACATGAC TCAGGGAGCA 1500 TCCGATGTGT GCCAGGCCTG GTGGCAGGAG CAGGGCCAGC TGAGTGTGGG ACATGCCCCA 1560 CTCTGGGGGT CTTCTCTAGG TCAGCATTAC AGCAGCCTTG GAGAAGACGG CTCCCACCCC 1620 TTCCGTCCTC CCCTCTCCTG GCTCCCTTGG GCAGCCTGCT CTGCCAGCCA CACCACACTC 1680 CACTTTCGGA TTCCGGAAGG AAACTATGGG TAATAAATAG GACAAAGGGT CAATTTCCTT 1740 CCTGTGCAAA TCCCAGTAGC ATTTGCAGAG TGCCAAGCAT GGGAGGGCGC CCTCCTAAGT 1800 GCTTTACCTG CCTTCACTCC ACCACAGCCC TGTGAGGAAG GTGCTCCCCT TTCACAGAGA 1860 AGGAAACTGA GGCTCAGTGA GGTGAGCAGC CTGGCTACAG TGGCACTGCC AGTGAGCAGC 1920 TGACCCAGCC TGTGACCTGG GCTGTGGCAC AGCAAACAGC CAGCAAGCAC TGGGTGCTTT 1980 TCCTGTGCTG GGCCAGCACT TTGCAGGCAT CGACTCAATT GAACCCTCAC AACCACCACA 2040 CATTGGTAAG AAAACCACCC TGACAGTCCT GGGAAAATGC ACAGTCTTAG TGCTCTGAAG 2100 GAAACAAAAA AGGACACATC AGTCATCAAA GAAAACAGAG AGATCCATCT GGAGTGCCTT 2160 GAATTGGCAA ATGGTTTAAT TTTCCTGTAT AGGGACGCTG GCCTTGCTGG GGCACCATGG 2220 AGCGGGGCCC 2230
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