Tag | Content |
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EnhancerAtlas ID | HS077-00441 |
Organism | Homo sapiens |
Tissue/cell | H128 |
Coordinate | chr1:44014970-44016780 |
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) |
KLF5 | MA0599.1 | chr1:44016018-44016028 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:44015762-44015772 | GGGGCGGGGC | - | 6.02 | SP1 | MA0079.4 | chr1:44015760-44015775 | GAGGGGCGGGGCCTG | - | 6.22 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_00616 | chr1:44009256-44025211 | Adipose_Nuclei | SE_04240 | chr1:44003988-44015177 | Brain_Anterior_Caudate | SE_05040 | chr1:44001099-44015486 | Brain_Cingulate_Gyrus | SE_05040 | chr1:44015834-44021066 | Brain_Cingulate_Gyrus | SE_05962 | chr1:44000439-44020958 | Brain_Hippocampus_Middle | SE_07193 | chr1:44016119-44020709 | Brain_Hippocampus_Middle_150 | SE_08033 | chr1:44003431-44015175 | Brain_Inferior_Temporal_Lobe | SE_08033 | chr1:44015878-44020741 | Brain_Inferior_Temporal_Lobe | SE_23218 | chr1:44005985-44017477 | Colon_Crypt_1 | SE_23829 | chr1:44013362-44015343 | Colon_Crypt_2 | SE_23829 | chr1:44015459-44017409 | Colon_Crypt_2 | SE_24870 | chr1:44012836-44017627 | Colon_Crypt_3 | SE_26649 | chr1:44010798-44020559 | Esophagus | SE_27645 | chr1:43995619-44017587 | Fetal_Intestine | SE_28595 | chr1:44005404-44017604 | Fetal_Intestine_Large | SE_31538 | chr1:44004919-44019003 | Gastric | SE_41575 | chr1:44001646-44015303 | LNCaP | SE_41575 | chr1:44015364-44020400 | LNCaP | SE_47657 | chr1:44013015-44015395 | Pancreas | SE_47657 | chr1:44015425-44018793 | Pancreas | SE_50363 | chr1:44005822-44020588 | Sigmoid_Colon | SE_52524 | chr1:44004832-44019377 | Small_Intestine | SE_56987 | chr1:44014752-44017377 | VACO_400 | SE_65452 | chr1:44004903-44018198 | Pancreatic_islets | SE_69138 | chr1:44014239-44017340 | 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 | 44015731 | 44016125 | chr1 | 44016660 | 44016751 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I043539 | chr1 | 44005459 | 44020850 |
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Enhancer Sequence | TGCCTGGGGA CCTGACACTG TGGGATCTGG TCAGTGCTGG GATGGGAAGC TCTGGGCACC 60 TCAGGCCATG GGACACAGAG CAGGCTCCTA CAGCAGCTTG GCTGGGTGGG ACATGAGAGA 120 GGGGCTGGGC TGGGCACACT CAAAGGCAGG GAGGAGTCTG AGGGCCTGGC CTGTCAGGGT 180 GGCCTAGGTG GTGGGTCCAA GCTGTGTGCT CTGCACAGTG CTAGGCCTGT ACTATAGTAG 240 GTGCTCAAAA AATACTTGTT GAAAGAGTAA AGAAGCCGGG TGTGGTGGCT CATACCCGTA 300 ATCCCAACAC TTTGGGAGGC CAAGGCAGGT GGATCGCCAG AGCTCAGGAG TTTGAGACCA 360 GCCTGGCAAT GTGGTGAAAC CCTGTCTTTA CCAAAAATAC AAAAAATTAG CCAGGCATGG 420 TGGTGTGCAC CTGTGGTCCC AGCTACTCGG GAGGCTGAGG TGGGAGGATT GCTTGAGCCT 480 AGGAGGTGGA GGCGGAGGTT ACAGTGAGCT GAGATTGTGC CACTTGTACT CCAACCTGGG 540 TGACAAAGTG AGACCCCCCT CTCAAAAAAA AAAAAGACTA AAGAAAAGTG AGCCTGAGAG 600 CTTAGGAGGA GCACATTTCA GAGGGGAACG GAGAGAGGAA CATCAGGCCC GTTGGTAGCT 660 GAGGAGAGGT GCGGTTAGAT CTGTGCTCCC CAAAGATCCT CTGCTGAACA TAAGGGGCAA 720 CGCCTTGTCT CCTGTGCTGT GTCCTGCGGG TGGAGGTGGA TTGGAGGGAA GCGGAGGGCG 780 AGGCCTGGTT GAGGGGCGGG GCCTGCCTGT CTGGTCCCCC GGGCTGCCTT GGGCCAGCTT 840 GGCCTAGTCT GTTGGGTGGG CGGGCAGGGT GCAGGCTCCT CTCCAGCCTC CAAGGGAGGG 900 GAGTTGTTCT GCCTCCTCGA TAGCCCCAGG CCTTGGGCAC AGCCCAGCCT CCCACGGCTC 960 TTGGGCCCTC CTCCTTCCAG GCCGCCGGTG ACCCACACCT GGCTCTCCTC CCCGGCGTCT 1020 CCTCTCCGCT TCTTTGTTTG GAGCGGAGGC CCCGCCCCAC CCCGCCCCCA GGCGCACTCG 1080 CCCGGCCATT CCGGTTCAGC CGGTTCCAGC CCCCAGTTTC TGCCGCTGCA GGTCCCGGCA 1140 GGAGCTGGAG GGGCACTTTC TCCCTGGGTT TCTCTTCCCT GGTGCAGCAG GGGCCGCGGT 1200 CCTCATCCTC CTGGTTCCTC AGTTCGGTCC TTCTTTCATT CTCCACCCCT GGGTGCCAGG 1260 AACTGGGTCA GACACTGGGA CAGGAATCCA GACAGGCATG CTATCTGCCC TGCCCAGGGT 1320 TATGTTCTAG GAGGGGAAGC AGCCATTAAT CAAACACCAA AAATGTGGAA AAGTAATAAT 1380 CTCACACGTG TGCATAATAA ACTGTGAGTG AAAGTTATAA GCTCGGCAGG TAGGTAATAA 1440 GCTAGGAGCA GTGCTGTGGG AGGCAAGGGA GTTACCCGGG AGTTTCAAAC TAGGAACTGA 1500 GCTCATAGGT TGGGGGCAGG GGGACTGGAG AAGGCAGTGA TACTTAAATG GAGAGCAGAA 1560 GGATGAATGG AAGTTAGAGT GTATGGCGGA GGTTGGCAGA AGCAGCAGCT TATGCAAAGG 1620 CCCTGTGGCT GCAGGGAACA TGACGTTGCT CTTTAGAGGA GCCAAAGCTG GGGCTCTGGG 1680 GAGAGCAGCT GGGTCAGACC CCGCGGCTTT GTCTGCCATA ACAGGTGTTT GGAGAGTGAT 1740 TCGGCAGGTC TTTGGAGGGT TTTGATAGGG CGGGGTGTCG GGGGAGGCTG TCAGCTCACT 1800 CTGGACACTG 1810
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