Tag | Content |
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EnhancerAtlas ID | HS034-00843 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr1:33219070-33221700 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr1:33221585-33221596 | GAAGATAAGAA | - | 6.02 | KLF16 | MA0741.1 | chr1:33219795-33219806 | GGGGGCGGGGC | - | 6.02 | KLF16 | MA0741.1 | chr1:33219551-33219562 | GGGGGCGTGGT | - | 6.14 | KLF5 | MA0599.1 | chr1:33219498-33219508 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:33219796-33219806 | GGGGCGGGGC | - | 6.02 | SP1 | MA0079.4 | chr1:33219495-33219510 | CAGGCCCCGCCCCTC | + | 6.22 | SP4 | MA0685.1 | chr1:33219495-33219512 | CAGGCCCCGCCCCTCCT | + | 6.32 | ZNF263 | MA0528.1 | chr1:33220523-33220544 | TCCCCCCCTCCCCCGTCCCCA | - | 6.03 | ZNF263 | MA0528.1 | chr1:33220656-33220677 | TGGGGAGGGGAGGGAAAGGGG | + | 6.2 | ZNF263 | MA0528.1 | chr1:33221575-33221596 | GGAGGAGAGAGAAGATAAGAA | + | 6.32 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_00938 | chr1:33219006-33222393 | Adrenal_Gland | SE_23116 | chr1:33219622-33222368 | Colon_Crypt_1 | SE_23802 | chr1:33219124-33219553 | Colon_Crypt_2 | SE_23802 | chr1:33219604-33220504 | Colon_Crypt_2 | SE_23802 | chr1:33220519-33221309 | Colon_Crypt_2 | SE_23802 | chr1:33221322-33221788 | Colon_Crypt_2 | SE_24863 | chr1:33219103-33221902 | Colon_Crypt_3 | SE_26629 | chr1:33219003-33222323 | Esophagus | SE_28121 | chr1:33220540-33221955 | Fetal_Intestine | SE_29204 | chr1:33219822-33221616 | Fetal_Intestine_Large | SE_31442 | chr1:33219069-33222394 | Gastric | SE_32998 | chr1:33219539-33221354 | H1 | SE_34017 | chr1:33218987-33219471 | HCC1954 | SE_34017 | chr1:33219830-33221722 | HCC1954 | SE_36587 | chr1:33219820-33221157 | HMEC | SE_41588 | chr1:33219113-33221709 | LNCaP | SE_47530 | chr1:33219105-33219467 | Pancreas | SE_47530 | chr1:33219506-33221824 | Pancreas | SE_50335 | chr1:33220528-33222187 | Sigmoid_Colon | SE_52480 | chr1:33219537-33222050 | Small_Intestine | SE_64801 | chr1:33219051-33219585 | NHEK | SE_64801 | chr1:33219594-33221668 | NHEK | SE_65538 | chr1:33218762-33221927 | Pancreatic_islets | SE_68878 | chr1:33219160-33221410 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 33221184 | 33221695 | chr1 | 33219489 | 33220800 |
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Enhancer Sequence | GAGACTTGGT CTCAAAAAAA TAAAAAAAAT AATAAAAAAA GGACCTACCT TACACAATTG 60 TGGATAAAAT GAAGTAATGC ATGAAAGCGG TTAGCACAGA GCCTGGCACA TAGTAAACAC 120 TAAGTAAAAG GGTGCTACTA TTTTGAACAC TGTAACTACA GAAATACAGT CAGTTCGATA 180 CATTTGTACA CACAGGCACG TGACAGTCAC GGGGAGGTGG CTGGTGGGCT CTAGCGGCAG 240 CAGGGCTGCG GATCCGCGTT CTCCCAGCTC CATTGCACTC CTCAGAGCGG TAGCCTCTGG 300 GCTGAGAGAG TGGGCAACCC GCCTGCCCCA CCTGGACTGG CCAGGCCTTC CCCTGTGCGC 360 CCTAGGCTGG GCGGCTCAGC CGGTCTCCCA GGTCCCGGGA GGGGCGGAGC CGACGGGATG 420 CGCGCCAGGC CCCGCCCCTC CTCCGGGCCC GCCCCCGGCC TGGCCATTGG CCGCAGAGCT 480 CGGGGGCGTG GTCGAGCTGG GGCTGGGGGC GCCCGCGGTG CCCGCCCGCG AGTCTCGCTG 540 CCTCCCTCCC GGGGCTGCGG GCCCGGCGGC CGGGCTGGCT GGGCCGCGCT TGGGTTCCCG 600 CGCCGGCTCC CGCACCCGCA ATGGGGAACT CACACCACAA GAGGAAGGCC CCCAGCGGTC 660 CCCGGGTCCG CAGCTTCTGG CGGTTCGGGC GGTCGGCGAA GCGGCCGGCA GGTAGGGGCC 720 GGGGTGGGGG CGGGGCAGGC AGGGAGGAGG GTCCCTACTG CGGTCGTCGC CACCGCTGCT 780 GCCCCCTCCC GGGGCTTGGA GGGTGTGAGT GTGGGGGGGT CGGGAATCCC CGCGCAGACC 840 CCACCCCTCA CAGGCACACG GAGACACACG TACACGGTAA TACCTACGGG CGGGCACACG 900 TACATGTTCG CAGTTTACAC AGTCACACGC ACAACACCCA CTCAAATGTA CGGACACGCA 960 GACACAGGAT CACATACACC ATCACACCCA CACTCTCGTA CCATCGCAGT AGGACGCACA 1020 CAGCCTGAGA CATAGGTACA TGTATACCTA TGCATGCGGT TTACACAGCC ACACGAACTA 1080 CACCCACGCG CAGATCCAGA CACACAGGCA CACAGTCGTT CACACACATC GGTCATGTGG 1140 GTACAGTTGC CCAGCGTCTT AGGCACACAG ATGTACACAC AGGTTCATAA CTGCACAACC 1200 AACCGGACTC GCATTCAGGC TCACAGCAGA CCCTAAGGCA CTCGGACACA CACGCTTATT 1260 TCCCAGATCT TAGCCCCCAA CAGGCTGAAG GCTGAAAGTT TGTAGGAGGG AGGGGAGACA 1320 AAGGTGGAAG GGAGAAGCTG GAAACCCGGG GCTGGAGTCT GGGGACCGCC TCCATCTGGC 1380 GCGATCGGGA GTCGGACTGG TTTTCTTGGC TCCCTCCCTA CCCCCACCCG CGCCACCGCG 1440 ACTTCTCCCC GCCTCCCCCC CTCCCCCGTC CCCACGGTCC CCGAGGTCGC CGCCGCATCT 1500 CCCCCTTTCA ATGCAGCCAC CGAGCTGGAA CGCAGCCCTT GCCGGCTGCT GCGGGATCCC 1560 TCCGCGGGTC ACATTCCAGG CTCCAATGGG GAGGGGAGGG AAAGGGGAAG GCCTCCAATC 1620 CCAAGAGATG GGATTCCTGT TTCCCCCAAC AAGTGCGGCA GTTCAGGGTA TCCCCGAGGG 1680 GCGCTGAAGG AGGGGCTATC GAGAGTGCCT AGTTACTGGT GAATCCAGAG ATGGGGGAAG 1740 GGCAGGGTGA TGGTACCATT CCCTCCTCCC CAAGATAGAG GGTCTTCAAC ATAGGCAGGC 1800 ACTTTAGCGA TACCTGTTGG TCTGGGGGAG TGAGGAAATC CCAGAGGAGG TGGAGTGAAG 1860 GGGGCCCTGC TGTGGTGGGA GAATCTACGG GTGTATTCCC AGGATGGCCC ACATTCCTAG 1920 AGATTCCGAA CCGGAGCTTG ATGATCTCAT CGCTCCATGG AGGGGGTGGT GGAAAGAGCC 1980 TGGGCTGGGA AGTGGGGGAC CTCTCCTCTC AATGAGGCTG TGGAATAGGC CCTGGTGACC 2040 TTGAGCAGAT TCCTTTCACT TGTCTGGACC ACTCTGGCTC CTACAGGGGT TCTGTCTGTG 2100 AAATCAGGGG CCCTAGGTGA CTTCTTGGGA CACTTACTGT TCTGGCTAGC CATTTCATGG 2160 ATGACGAGAC TGAGGTCCAG GAAAGAGGGA CTTGTCCAAG GTCATTTGCC TGTGGTGGTT 2220 TGAGGTAGTA ATATAATCAA AATGACAATA AGAAAAGGGT TAACTAAGTT CAGTTAGGCT 2280 CTTTGAGGAT TTCTCAGAAG GTAGGTGTTG ATGAGAATCT CCAGGACCTT CCAGCACTCT 2340 CCCTGCCCCA GCAGTCCTGA AAGCCCTGTC TGTGCCTACC TGTCTCTCCT AGAATCTGCA 2400 CTAAGGGGGC AGGGCTGGGG CTCTTCATCT GTCCTCTGAT GGTCGCTCGG ATCTGATGGT 2460 TTCCTAGGAA CTAACTGTGG GCCCAGACTT GTGACCATTT GTGATGGAGG AGAGAGAAGA 2520 TAAGAAGGCT GTGTTTATAG TCTCTTGCCT ACTGGCCCTT GAGGAAGTGG CCTGGGGCTT 2580 CCAGCAACAC TTGTGAGCTT CCAGTTCCTG CTGCAACTTA TGGGTCAACT 2630
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