Tag | Content |
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EnhancerAtlas ID | HS108-28729 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr3:129321580-129324170 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr3:129322775-129322786 | GGAGGGTGTGG | - | 6.32 |
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| Number of super-enhancer constituents: 35 | ID | Coordinate | Tissue/cell |
SE_00112 | chr3:129305417-129325570 | Adipose_Nuclei | SE_00978 | chr3:129321697-129323153 | Adrenal_Gland | SE_00978 | chr3:129323570-129325703 | Adrenal_Gland | SE_01893 | chr3:129320358-129325457 | Aorta | SE_04322 | chr3:129319668-129323752 | Brain_Anterior_Caudate | SE_05345 | chr3:129310701-129325499 | Brain_Cingulate_Gyrus | SE_05951 | chr3:129308023-129325521 | Brain_Hippocampus_Middle | SE_07365 | chr3:129320968-129325546 | Brain_Hippocampus_Middle_150 | SE_08750 | chr3:129311577-129324158 | Brain_Inferior_Temporal_Lobe | SE_09767 | chr3:129321251-129323545 | CD14 | SE_25754 | chr3:129320148-129325522 | DND41 | SE_26494 | chr3:129322626-129323696 | Duodenum_Smooth_Muscle | SE_27065 | chr3:129320439-129327730 | Esophagus | SE_29874 | chr3:129321554-129323225 | Fetal_Muscle | SE_31569 | chr3:129320973-129323348 | Gastric | SE_31569 | chr3:129323423-129327747 | Gastric | SE_33524 | chr3:129321014-129326721 | H2171 | SE_37506 | chr3:129321224-129323754 | HSMMtube | SE_37994 | chr3:129310132-129325566 | HUVEC | SE_40701 | chr3:129308079-129325658 | Left_Ventricle | SE_42115 | chr3:129307923-129325621 | Lung | SE_46476 | chr3:129321099-129324056 | Osteoblasts | SE_46996 | chr3:129321736-129322814 | Ovary | SE_46996 | chr3:129322871-129323297 | Ovary | SE_47266 | chr3:129310010-129324076 | Panc1 | SE_48609 | chr3:129310376-129325641 | Right_Atrium | SE_49818 | chr3:129323622-129325482 | Right_Ventricle | SE_50249 | chr3:129319807-129325616 | Sigmoid_Colon | SE_51354 | chr3:129310040-129325518 | Skeletal_Muscle | SE_52687 | chr3:129320970-129325489 | Small_Intestine | SE_53375 | chr3:129320912-129328307 | Spleen | SE_62855 | chr3:129293187-129347490 | Tonsil | SE_65523 | chr3:129321577-129323275 | Pancreatic_islets | SE_65523 | chr3:129323511-129324084 | Pancreatic_islets | SE_68869 | chr3:129320930-129322808 | H9 |
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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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Enhancer Sequence | TAATGTCCCT TAGAGTAATA ACAAGAAGAA CTGCCATCTG CTTGGTGCTT ACTGTGTACT 60 GGGTACACTG AGCTGCATTT ATCGATTCAT CTAGTCCTTA AAACAATGCT TTGGGATAAG 120 GATTGCTTTT ACTGTCCCCA CTTCACAGAT GAAGAAACTG AGGCCCAGAG AGGTTAAGTT 180 CCTTGGCCAA GGTCACACAG CTGGGAAGTG ACAAAGTGGG ACTTGAACCC AAGCAGCCTG 240 ATGCAAAGTC TAGGTTCTGA ATCTGTCGCT GCATAGCTGG CAACAGCCTG GAGCAAGAAT 300 AATGATCCCT CCCCCACCCC TGCCCATGCT AGAGGCCCAG ACCGGGGACC TTGAGCACCT 360 CTGGGAGATA CTGCCAAGTG GCACTGGCCT GTGCCCACAG CGGGCACGGC GAAGAGGAGA 420 AGGGTGTGGA AAACACAGGG AGGGTGACCA AGGAAGGCCG CAGCCGGAAT CTGTGGCCTT 480 GGGGTGGGGA AGAGGCCCTT CGCCACTCTG TCCTGGGGCT GTGTCCCTGG AGAGGCCCTG 540 TCCCCTTAGG TAGAGAAGCT CCAGCCCCCC TCAGCTGGGT GAGTCACTGC ACCGAGGGAG 600 CGGACCGTGG GAACCAGAAT GGTTCTTGCC AGAGGGGGAG GGAACCCTGG GCTGGCCTAA 660 GGAATCCCAC AGATCAGCTT ACACCAAAGG GCCGAGACAC AGGGCCTGAA ACTACTGGAG 720 GAAGGCCCTC AGTCCACAGG ACACTTCTCT CCATTCAGCG ACTCCCCACT GAGACCCCCA 780 GTGCCAAACA CAGTTGCCTG CGAGATGAAG CTCTGGGGTG GAGATGGTGG ATGAACCAAC 840 CATGGCACAG GGCAAGCAGC CCCACCACCC TTTGGACTGT CTGCCCTGCT CACCCACCGT 900 GACCTTTACT TTCAGGGTGG CCGGCCAGAT GGTGGGCAGT CGTGGGAGAC CGACCTCGAC 960 CTTGGGAGAA GGAATCTGCA TTTTCTCAAA GCCCCAGTGT TGGGCCCGCC CACAGAGGAA 1020 TGGTTAATCT CATGAAATTC TTGTCACAGC CATGGAGAAG GGACAGGGTG GGGCCCCAAG 1080 GAAGGCTTGG GTCACCACAA GAAGGCTGAG TTCTGCATTT TGCTGATGGA GATGCAGCTT 1140 CCTAAGGGAA TGGCAGGCAG TGGAGCTGAA GTGGGCTCGC CAGACTCAGA TGGGTGGAGG 1200 GTGTGGGAAA GGCCCCAGTG TCATTCTGGG GCCTCATTCC TCAGGGTGAA CTATGGGGAT 1260 CAACAGACCC AGCTCCCAAA GCCAGTGTGA GGAGCAATCC CTTGCCATGA ACTTCCTTTC 1320 AGGGAACCAC ACCAAGTCCC CTCCCGCACC CTTGTCATGT CAACACACAT GCTGATTCCG 1380 TCAACCTGGC CCCCCTTGCT ACTGCCCAAC CCAGCCTCAG ACACCTGGGC CCCATGCCTG 1440 CCTGTACTCC TCCTCATTCC CCACTGAGCC CCACGGCCCT CTCCTGCCCC CAAAACACCC 1500 CTGTTCACAT CCCTCCATTC TCCTGGCCCT GGCATCTGCC CACCCCAGCT GCCTGGGACG 1560 CCCCCAAAAC ACACGCACTC TGAGATCCAA GTCCAGAAGG CAGCAAAGGC TGGGCATTAA 1620 AAACACAGAT GCTGAGGCCA GACAGGCTGG ATTCAAATCC ACCTCTGCTA GTGCCCAACT 1680 GTGTGATCCT CAGCAAGTTG CTTAACCTCT CTGTGCCTGT TTCTTCATCT GTAAAATGTG 1740 ATGAGAATAG AGGCTACCTG AGAGGGTTGT TCTGAGAACT GGGAATTGTG ACATGTGATG 1800 CCCCTAGCTG GCACTCCACA AGTGCTATTG TTTACCCCAG ACTCCCACAC CTGGTACATA 1860 CTAGGTGCTC AGGAAATATT TGCAGAATAG GTGAATAAAA GTTGGCCTCA GGCACACACC 1920 TGTTTGCCAA CCATGCAGCC TCCTCAGAGT ACCGACTCAT GCCCAAATAC CTGCGTCCCC 1980 TGCCACGCAC ATCCCACTGC ACACCTAGCC CTGTCCCGTT GTACCAGTGT CTGTGCAGTA 2040 CACCTGTCTG CCCTGTGCGT CTTCAGGCCC CAGCTTGCTG GCACACAAGT CCATGCAGAC 2100 ATCTGCAGGG CCCTGGTGCA CACCTGTGTG CCTCCTTGCA CACCTGCCAC ACCCATGCAC 2160 CCATCACCAA CGTGCAATGG TAACTCTGAC AGGCTCACGC AGTGGCCCCA GAACACAACT 2220 TTGGTCAGGC ATGCAGTCAC TTACTGCGCC CTCAGCATGC ACCTGTGACC CTCACGTGCA 2280 TACCTGGGCT TTATGCGCAC CTGGGTACCT GTGGCAACTT GGACCCCTCC CAGTACGCCT 2340 AGGTATGCGC GCCCATGAGC CGGCACTCAC TTGAGTCCCT GCACATGCCC ACCTGGGCCA 2400 TACAGGCGCC AGTAGTACCC CTCGGGGGAC ACCTGTATTC TCGCGTGCAC ACCTGGGTTC 2460 CACGTACATC TGGATCTCTG CGCGCTCCCA CCTGTGACCC ACTCAGCTCA CGACCCGCTC 2520 GGTTCCCGCC CGCCCCCGCC CCCGCCCCCG CCGCCGCCGC CGCCGCCGCC GCCGCCACCG 2580 CCCGGGTGTA 2590
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