Tag | Content |
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EnhancerAtlas ID | HS036-00002 |
Organism | Homo sapiens |
Tissue/cell | endometrioid_adenocarcinoma |
Coordinate | chr1:1002580-1006470 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF14 | MA0740.1 | chr1:1004737-1004751 | GTGGGGGCGTGGCC | - | 6.39 | KLF16 | MA0741.1 | chr1:1004739-1004750 | GGGGGCGTGGC | - | 6.62 | KLF5 | MA0599.1 | chr1:1004502-1004512 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:1004521-1004531 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:1004157-1004167 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr1:1004196-1004206 | GGGGCGGGGC | - | 6.02 | Klf1 | MA0493.1 | chr1:1005572-1005583 | TGGGTGTGGCC | - | 6.62 | NRF1 | MA0506.1 | chr1:1004721-1004732 | GCGCCTGCGCG | + | 6.14 | RFX1 | MA0509.2 | chr1:1004774-1004790 | CGTCGCCATGGTGACC | + | 6.11 | RFX1 | MA0509.2 | chr1:1004774-1004790 | CGTCGCCATGGTGACC | - | 6.12 | RFX2 | MA0600.2 | chr1:1004774-1004790 | CGTCGCCATGGTGACC | + | 6.2 | RFX2 | MA0600.2 | chr1:1004774-1004790 | CGTCGCCATGGTGACC | - | 6.2 | SP1 | MA0079.4 | chr1:1004499-1004514 | CAAGCCCCGCCCCTC | + | 6.34 | SP2 | MA0516.2 | chr1:1004498-1004515 | GCAAGCCCCGCCCCTCA | + | 6.23 | SP3 | MA0746.2 | chr1:1004738-1004751 | TGGGGGCGTGGCC | - | 6.57 | SP4 | MA0685.1 | chr1:1004499-1004516 | CAAGCCCCGCCCCTCAT | + | 6.24 | SP8 | MA0747.1 | chr1:1004738-1004750 | TGGGGGCGTGGC | - | 6.11 | ZNF263 | MA0528.1 | chr1:1003831-1003852 | CCTTCCTCCTCCTCCTGCTCG | - | 6.88 | ZNF263 | MA0528.1 | chr1:1003819-1003840 | CCCTCCCCATTTCCTTCCTCC | - | 6.89 | ZNF263 | MA0528.1 | chr1:1003825-1003846 | CCATTTCCTTCCTCCTCCTCC | - | 7.03 | ZNF263 | MA0528.1 | chr1:1003822-1003843 | TCCCCATTTCCTTCCTCCTCC | - | 8.3 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_24070 | chr1:1002554-1005867 | Colon_Crypt_2 | SE_24817 | chr1:1002490-1006081 | Colon_Crypt_3 | SE_27529 | chr1:1001798-1011077 | Esophagus | SE_34539 | chr1:1002321-1004360 | HCT-116 | SE_34539 | chr1:1004454-1006480 | HCT-116 | SE_41944 | chr1:1001963-1005965 | LNCaP | SE_58139 | chr1:1003761-1004209 | VACO_9m | SE_58139 | chr1:1004236-1004768 | VACO_9m | SE_58139 | chr1:1004812-1005267 | VACO_9m | SE_65935 | chr1:1001682-1006445 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr1 | 1003459 | 1003600 | chr1 | 1005293 | 1005547 | chr1 | 1006044 | 1006328 | chr1 | 1003600 | 1006245 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I001066 | chr1 | 1001837 | 1006486 |
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Enhancer Sequence | TGGCCTCATT CCCTTTCAGA CTGACCCTGA GGAGGAGCCG GGCCATGGCA GGGGCAGGGT 60 GGACATCCCT TGTGGCCCTG CCCCGCCGCA CCTGCACCTG CACAGCCCGC GTGGGCCCGC 120 CCCGCCGCAG CTGAAGTGCA CCACCATGGG CCCGGCCCGC GGCTCGCGGC TCGCGGCTCT 180 GGGCCCGGTT CACCTCGTCC CGGAAGCCGA GGACGCCGGC GGGATCGGTC CGGACGCCGT 240 AGTCCGGCCA GCCGAAGTAC TGGAAGTGCT GCACCGTACG CTGTGGCTCC TCCCCGCGGG 300 GCAGGGCCTC GCGGGCGCAG GGTGTACATC GCCTGCAGGG CTGTCTGCAG GCCTGTCTGC 360 AGGCCACGGT GGCTGCTTTC TGGGCCACGG TGCACCAGGA GAACACGCGT GTCATCGTCA 420 TGACCACCAG GGAGATGGAG CGGGGCCGGG TAGGGGTGCG GTGCCAGTGC TCCCAGTGCC 480 CATCCCACCC CGTGCATCTT CGGCTGCCCA AGGCCCTTCC CGACCAGGCC AAGGAGGCTG 540 TGGGACGCCG TGGGAGTGGG GAGGCTCCCA CAGAGCCCCG TGGCTGCACG TACACACCTG 600 CGTCTCTGCA GGTCGCAGGG GCGGGGTGCC GAGGTGCTGC CAGCAAGGCT GATGCAAAGC 660 GCTCCCCTCG GAACAAGTGT TTCCGGGACT GGCCAGAGCT GCCCGGCAGC CAAGAGTTCG 720 GCCGTGTGCA CATGCGCGTC CTCGGCAAGG GCCAGGCCCA GGGCTACTGC GTGCGGGAGC 780 TGCAGGTGTG GCGGCCGGGC CAGGTGAGCC TGGCGGCTGT GGAGCGTGCC TGCTGTCGGC 840 CTGCACTGGG AGACCCCACA CCTGCCTGCA TCCAACCCCA CTGCCTTTGG GGGCTTCCAC 900 ACCCCTCAAC CCAGGAGGTG CATTCCAAGC CTGGACAGGG GTCACTGACG TGGCCACATT 960 CTCAGCCCTG GGCTGGCGGC CGCTCCTCCC ACACACCTCT CCAACTGCAG CTTTGGTCTC 1020 CGTTGTATAC CAGAGACGCC CATTTCTGCT CCGGGCAGAT TACCTCGTGT TCCCTCCAGC 1080 CCCCGCCCAG TGTGTGTGGG GGGGTCCTCC AGGACCCCAT GGACCCCTCA CATTTGGTTT 1140 TTCCTTATAA AATAACTGTC CTCACAGCCT GCTTCGCCCG CCCCCAGCTC CCTCTTCCCT 1200 TCCCCAGGCA CCTGAGCCAC CTGGGGCCAT CTCGGCGCCC CCTCCCCATT TCCTTCCTCC 1260 TCCTCCTGCT CGCCTTGGCT CCCGCAGCCC CTCCGCTTGG GCACTCCCGG AAACCCAGCT 1320 GTGCCTCAGC CTCCTCCTCC CACCCTGGGG TCACACTCAC CGCTTGCCCC GCTCAGGAGG 1380 AGCCACAGCG TACGGTGCAG CACTTCCAGT ACTTCGGCTG GCCGGACTAC GGCGTCCGGG 1440 CCGATCCCGC CGGCGTCCTC GGCTTCCGGG ACGAGGTGAA CCGGGCCCAG AGCAGCAAGC 1500 CGCGGGCCGG GCCCATGGTG GTGCACTTCA GCTGCGGCGG GGCGGGCCCA CGCGGGCTGT 1560 GCAGATGCAG GTGCGGCGGG GCGGGGCCAC GCGGGCTGTG CAGGTGCAGG TGCGGCGGGG 1620 CGGGGCCACG CGGGACGACG AGGGCGGAGC CATCGGGTGG GCGGGGGCGC CCCCGCCCCC 1680 GCCCCCCACT CTCGTCAAAG GCCGCCTAGT TTGTCCTCAG TGGGGGCATC GGATGCACGG 1740 GCACCATCAT CGTGATTGAC ATCCTGGTGG ACGTCATCCG CAGGCAGGGC GAGCCGCTCC 1800 ACTCTGGGTC CCCCCGCCCT GCCCTGCTAT AGCCCCACCC CTCCGGGCGA CCCCACCCCT 1860 CCGGACGACC CCACCCCTCA GGACGACCCC ACCCCTCAGG ACGACCCCAC CGCTACCGGC 1920 AAGCCCCGCC CCTCATCAGC AGCCCCGCCC CTGCCTGCCG GCACCTTCCC CCCATCCGTA 1980 GCCCCTCCCC AAGCGCGCTT GTCCGCAGGG CTGGACTGCG ACACCGACGT CCCGAAGACG 2040 ATCCAGCTGG TTTGGCGGCA GCACTGGGGA ATGGTGCAGA CGGAGGCTCC GTACAAGTTC 2100 ACGTACCTGG CGCTGCAGCG GCACATCCGG GGCGAGTAAC TGCGCCTGCG CGAGCAGGTG 2160 GGGGCGTGGC CCTGCGGGGC GTGGCCTGTG CGGGCGTCGC CATGGTGACC GGCGGCCCCT 2220 CCCCCCAGCG CGAGCCGCCT CAGGAGCGCG AGAACCAAAA CGTGGGCGCC GCCCCCCGCT 2280 AATCGGGTTG CAGCCCCCGG CTCCCCGGGC ATCCCCGGTG TGAGTGGAGC GCCGGGGCCG 2340 GTCCGGAGTC CTCTGGGAGG GACTGGGACG TGCGGGGTGC AGGGCTGAGC CGCTGCTCCG 2400 CGCGCAGAAC CCCGCAGCCC TGGGACGGCG AGGACGCGAA CCTGCGGAGC CGCGGGTGTC 2460 TGAGGAGCCG CAGGGAACCC CCGGCCTAGC CGCGCCCGCG TGTGGCCGGA GCTGCGGGCC 2520 GGGACTGTGT CCAGGACAGA GCCACAAGCT TGTCCCCAGC TCAGGGAGGT CCAGGGGCGG 2580 CAGAGGGAGC GACAGGCTGC GAAGCCCACC GGTGACCACG TGTGAACCCG CGTGCGCCCC 2640 CAGCTCGGCC ACTCCGTGCG GGTCTGCCCT CACCGCAGCT CCGGCCTGCC GGCCCTGCCT 2700 GCTCCCGTGG TCTGGGATGT GGCCCCGGTG AGGACCCGGC CCCATCAGGC ACAGGGTGGA 2760 TGTCTGTGGA GTGAGGTGTG TGTGACATAT TCATGTGACC ACCCGTGCAG CGTCACGCGC 2820 CTGGCCCTGC CGATGACAAG GGTGTGGGCC TGCGTGGGCA TGACTGTGTG TGTGACACAG 2880 AGTGATGTTG CTGTGACCCG TGGCTGCACT CCCCACATCA CCGGCTTTCA CAGCCTTCCG 2940 GTAAAGTGCT GTGTTCTCCC TTCTGTGTCT TCGCTGGGAC CTGGGGCAAG GGTGGGTGTG 3000 GCCCCCACAG CTGGAGTCAG CTTCTGTGGG GCCTTCCCGA GCCCTCCCCA CCCTGGACCA 3060 GAGGCCCAGC TGGTTGGAGC AGGAAGTACC TGGGCTCTGG GGTCAGGGAT GGGAAGGCTG 3120 AGGAGGCCTG CGTGAGCTGG ACCTGGCCTG GGCCCTCCTG GCCGTGCCTG CCTGGTGGTG 3180 CAGGATTCCT GGGGCTGATG ACAGACGGGG TAGGGCTGGG GTTGGCGAGC CTCCTGCCGA 3240 TACCTCACGT AGCTGACCTC TGACTCTTCC CCAGCCAGGC TGGCCCTGGG AGTTGCCGGA 3300 GAGTCAGTGG ATCTGCAGGC TGCACGCTGG CTGTTACCTT TGCTTCTGGG TTCCCACAGG 3360 GGTCATGGTT CTGTGGTTCT CCAGTCAGGG ACCCTAGCAG GGCCATGGGG CGTGACTTCC 3420 TGGAGGTGTG GCCTAGTATG GCCACGGCAG AGGATGGGGG AAGAGAAAGG CCCCCTTTGT 3480 CAGCCCCCGG GCTCTGAACC AAGCTGAAGC CCTCCCCCTG GTCCAGCCTG CCCTGCCCCA 3540 AGTGTCCTGG GCCTCTCCCC ATCTCCCTGG GGAGCCTCAC ATTGCTGAGT CGCCAGCCAA 3600 CTCCAGAAAC CCCCAGCCTG TCTGCAGCCA GAGGGGCTGG GAGTTGGACC CCCTAGAACC 3660 TTGGGCCCAC CTGTCCCAGT GGCTGCTGGG AGTCTAATTC TGTCAGGGTA TCCTCTGGGT 3720 TGAGGCTGCA GCAGGGGCAC CCAGGGTGAG GCCCTCTTGC CAAAGATGGA TACAAATAAT 3780 TTATTTTAAA AGGTACAATT CACAAGGTTG GAGGGGTAGC TGGAAGTTTC TGTGGTTACC 3840 TTGCACTGGG GGGCTGCCCT GCCTCCACTC TCTCCCCACA GTCCGAGGGC 3890
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