Tag | Content |
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EnhancerAtlas ID | HS193-00310 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr1:16501790-16503570 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6B | MA0731.1 | chr1:16503374-16503391 | TGCTTCCTAGGAAGTGA | + | 6.08 | RREB1 | MA0073.1 | chr1:16502026-16502046 | TGTGAGGGGGTGGGAGGGGG | - | 6.61 | RREB1 | MA0073.1 | chr1:16502036-16502056 | TGGGAGGGGGTGGGATGGGG | - | 7.16 | SOX10 | MA0442.2 | chr1:16502839-16502850 | TTCTTTGTTTT | - | 6.62 | ZNF263 | MA0528.1 | chr1:16503057-16503078 | CATCCTCCTCCATCCTCCTCC | - | 6.3 | ZNF263 | MA0528.1 | chr1:16503060-16503081 | CCTCCTCCATCCTCCTCCTCC | - | 8.07 |
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| Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
SE_23091 | chr1:16501962-16502745 | Colon_Crypt_1 | SE_23091 | chr1:16502844-16503560 | Colon_Crypt_1 | SE_23751 | chr1:16502050-16502674 | Colon_Crypt_2 | SE_23751 | chr1:16502855-16503434 | Colon_Crypt_2 | SE_24743 | chr1:16497841-16502803 | Colon_Crypt_3 | SE_24743 | chr1:16502816-16503501 | Colon_Crypt_3 | SE_26540 | chr1:16496436-16504779 | Esophagus | SE_28102 | chr1:16497879-16504574 | Fetal_Intestine | SE_29455 | chr1:16497964-16506131 | Fetal_Intestine_Large | SE_31527 | chr1:16499336-16504399 | Gastric | SE_34268 | chr1:16497740-16504248 | HCT-116 | SE_34628 | chr1:16497415-16506115 | HeLa | SE_36144 | chr1:16502024-16503485 | HMEC | SE_38062 | chr1:16499064-16503878 | HUVEC | SE_40833 | chr1:16501759-16503971 | Left_Ventricle | SE_44998 | chr1:16502053-16503662 | NHLF | SE_46140 | chr1:16501795-16503844 | Osteoblasts | SE_47009 | chr1:16502010-16502676 | Ovary | SE_47009 | chr1:16502860-16503560 | Ovary | SE_47150 | chr1:16499250-16512083 | Panc1 | SE_47539 | chr1:16501964-16502662 | Pancreas | SE_47539 | chr1:16502819-16503601 | Pancreas | SE_48744 | chr1:16501448-16503785 | Right_Atrium | SE_50427 | chr1:16497958-16504232 | Sigmoid_Colon | SE_52536 | chr1:16501918-16504326 | Small_Intestine | SE_56795 | chr1:16499345-16504738 | VACO_400 | SE_57357 | chr1:16501943-16502709 | VACO_503 | SE_57939 | chr1:16501961-16502682 | VACO_9m | SE_57939 | chr1:16502843-16503425 | VACO_9m | SE_64726 | chr1:16502266-16503212 | NHEK | SE_65472 | chr1:16501980-16503977 | 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 |
GH01I016171 | chr1 | 16497941 | 16511884 |
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Enhancer Sequence | TCATGAGACT TGGGCAAGTG TTTTAAGCCC TCGGAGCCTC AGTTTCATGA TCTGTAAAGT 60 GGACATTAGA GTCGCTCGGG ATGCGGGATG CTTGAATGAG ATGATGCACT CAGCACGCGG 120 CAGGCCCTGG GGCCCTGTGT GCTCTACAAT TGCAGCTGCT ATTAGACCAG CTTCTTTCTT 180 GCCTGGGTAT GTGGGGCTTA GGCCAGAACA AATCTTGGGA CTGAGTGTAA AATATATGTG 240 AGGGGGTGGG AGGGGGTGGG ATGGGGCTCG GTGCGGGCCT GGCAGGTGTG CTGGGAGGCA 300 AGGCCTATGA CTCCTGTGGG CCTGCTCTTC CTCCCATCCC ACCCTCCACA GTCCCCACCT 360 CAGGGGCCCT GGGCCTGGGG CAGCAGGGGC CGGGATGTGT CTCTCCAGAG CAGGAACGGA 420 GGGGCCTCCG CAACTGGTTG GGGAGGGGGG GTGGATGCCA GCCCCCGCTG ATTAGGTCTC 480 AAATTAAAGC CGAGCTTGCT CCTGTCGCTG CTCAGGCAGG CCCTCCTCCT GGCCACAGTT 540 CCCTGCCTGG CCCTCTGCTT CGGGCCTCAT GGTGGCTGGT TGCTCCCAGC CTAGAATTGC 600 TAAAAGGCTC CCGTAGTGGG TAGGAGCCTC AGGGGACCTG GGAGAGGCTT CAGGGGCCCT 660 GCCTGTGCGG GGGTCTCTCC TGTGACCCTC AGACCTGAGC CAGTGTCTGG GGACAAGTCA 720 CCGTGTCAGA GGCTGCGGAG AGCAAAGCCC AGGCGGTGAT GACTTGAGTT TCCAGGCCGG 780 GTGCCAGGAG GCCCGCGGTC ACACTCCGCC TGGGGCCTGG GCTCCGGCCA ACTGTCAGCA 840 GCAGAGATTG TTGGGTTGGT TTTATTTTAA ACAAAAAAGA ACTTTGAGTG GAAACATGTG 900 TTTCTTTTTT CTCCCCCTTC CCTCTCTCCC TATCTCTCTC CATCTCATCA TGGAATATTT 960 CTCTTTTTTG TACCTCCCTT TCTCTGTTTT TCTCTCTGTC TTCCTCTATT TGTCCCTGCC 1020 TCTGTCTCTC TCTCTCTCTC TCTCATTCTT TCTTTGTTTT CCTATCTCTT GATTTCTCTG 1080 TCTCTTTCTC TATTTCTTTT TCCGCAGCTT TCAGGAGTCA GGAGAGGTAC CAGACTTCCT 1140 CCCTCGGGGT GTGGCCTGGG CCCCTGCCAT AAAATCCCCA GGCGTGCCAC GGCCCTATGT 1200 CGGGGGTCTG CCGCTCCAGG GGAGGGAGGG GGTGTCTAGC AGCGGAGGCT CCAGGACCCA 1260 AATGCTCCAT CCTCCTCCAT CCTCCTCCTC CAAGCTCCCA CTGCCCCTGC ATCTGCCCTT 1320 CCTGTGTCTG TTTTCTCTAC TAAGCATCTA GAAAATAATT CTGCAGCTTG AGACAAGTTT 1380 TAAAACACTG GTCTGGCCCA AACCACCCAT CTACAGCCAG AGACTGGCGC CGAGGAGGGG 1440 ACCATGGCCT GCTCAACACC GCACGGAGGG TTAGGGGCAA AGCCAGGCCG ACCCAGGTCC 1500 CCCACTCCCA AGTGACATTA CTGACACCCC CAAACCCACA GTCACCACAC TTCTCAGGTC 1560 CCTGCGTCTT TCAGAGGGGT GGTCTGCTTC CTAGGAAGTG ATGTGCCCTC CCCTAAGGTG 1620 GTCACCCAGC ACAAGGGTCC CCCTGGAAAA TGTCCTGCCT TGGCTGGTCA CCCCTCCCCC 1680 AGGACAGACA AGCTTTTGGG CCCCCACCTT TCAGCCCCTT CTGCCAGGCA GTAGAGAAGA 1740 GAGAAGAGAG ACTCGCAGGC ACAGTGGCTC ATGCCTGTAA 1780
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