Tag | Content |
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EnhancerAtlas ID | HS134-00500 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:22235750-22237940 |
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) |
Myog | MA0500.1 | chr1:22237908-22237919 | GACAGCTGCTG | + | 6.14 | Tcf12 | MA0521.1 | chr1:22237908-22237919 | GACAGCTGCTG | + | 6.02 |
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| Number of super-enhancer constituents: 39 | ID | Coordinate | Tissue/cell |
SE_00032 | chr1:22219419-22267496 | Adipose_Nuclei | SE_00908 | chr1:22235514-22242299 | Adrenal_Gland | SE_01556 | chr1:22235059-22242385 | Aorta | SE_02999 | chr1:22235920-22237166 | Bladder | SE_02999 | chr1:22237345-22237955 | Bladder | SE_06476 | chr1:22235474-22238889 | Brain_Hippocampus_Middle | SE_13865 | chr1:22227437-22237425 | CD34_Primary_RO01536 | SE_23160 | chr1:22237333-22238567 | Colon_Crypt_1 | SE_23793 | chr1:22237648-22238327 | Colon_Crypt_2 | SE_24796 | chr1:22237541-22238537 | Colon_Crypt_3 | SE_25801 | chr1:22235294-22242489 | Duodenum_Smooth_Muscle | SE_26605 | chr1:22235509-22242357 | Esophagus | SE_28012 | chr1:22235488-22242414 | Fetal_Intestine | SE_28954 | chr1:22235552-22242440 | Fetal_Intestine_Large | SE_29681 | chr1:22234910-22242400 | Fetal_Muscle | SE_36920 | chr1:22219607-22267740 | HSMMtube | SE_37945 | chr1:22220303-22255266 | HUVEC | SE_39947 | chr1:22234842-22236953 | K562 | SE_40620 | chr1:22234922-22242399 | Left_Ventricle | SE_42167 | chr1:22234999-22242386 | Lung | SE_44366 | chr1:22235089-22239328 | NHDF-Ad | SE_45173 | chr1:22235732-22237092 | NHLF | SE_45699 | chr1:22234847-22242422 | Osteoblasts | SE_46764 | chr1:22235798-22237204 | Ovary | SE_46764 | chr1:22237309-22239252 | Ovary | SE_47433 | chr1:22235733-22240874 | Panc1 | SE_47860 | chr1:22236045-22236448 | Pancreas | SE_47860 | chr1:22236562-22236821 | Pancreas | SE_48478 | chr1:22235486-22242245 | Psoas_Muscle | SE_48565 | chr1:22235175-22242369 | Right_Atrium | SE_49456 | chr1:22235561-22237122 | Right_Ventricle | SE_49456 | chr1:22237167-22238544 | Right_Ventricle | SE_50206 | chr1:22235495-22242384 | Sigmoid_Colon | SE_51733 | chr1:22235366-22239269 | Skeletal_Muscle_Myoblast | SE_52462 | chr1:22235524-22239350 | Small_Intestine | SE_53700 | chr1:22235033-22242399 | Spleen | SE_54522 | chr1:22234975-22242507 | Stomach_Smooth_Muscle | SE_63519 | chr1:22235220-22240758 | HSMM | SE_68865 | chr1:22235783-22238487 | 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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| Number: 1 | ID | Chromosome | Start | End |
GH01I021893 | chr1 | 22220486 | 22243088 |
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Enhancer Sequence | CAAAGATGCA CACTTAACAG CCAAGAGAAT ATTAACTAAA GAAATATAAG AAAAACTCAG 60 GCAGGGCAGG CAGATGGAGC CTGGAGTGAG GCAAGCAGAC AGAGAGCACA TGCTGAATCC 120 CAGAGATCTA GGAAAGGGAC AACTCATGTG GCCCTGAGCT TGCCAGCAGC CAATGGGAAG 180 AAGGAAACCT GACCAGTCCC TAGATTCCAT GTCTCACAAT GTAAAAACAA ACCAGTTGCT 240 TAGAAAAAGC ACAACTATCC CTGATACTGA GAGCAGGGAA TGTCCCAAGG GACAGGCTTG 300 TCTGGCACCC TTCTCTGCCT CATCAGTGGG GCTGGCATCC CCTCAGAGTC TGCTGACCAT 360 GACCCTTTGA AGCTGAAGCC AGGGGCAGAG GCTACAGTGA TCAAAGATTC AGGGAGCTGG 420 AATGGCAGTC CAGTCAGTAC CCCACCAACC TCACCCCAGC AGCCTTGGTC TAGGCAGGAT 480 TACCCATCAC TCCCCAAACC CGAACACAGC CAGTGCCCAA AATAGCTAGA GCAGGAGAGG 540 GTGCCAAGAG GCCCTGGCAA GGGCCTGGGC TAGGCCCACC TACAGGAGGG CCCAGTGGGC 600 CAATGCACAC ATACCTCTGG TGCACAAAGA GGCACCTTCA GTCAGGCACA GAGCCGTCCC 660 TGGGAGTCCC CCACCCACCA GGCTCCCCCC TCAGCTGCAC GTTGCTCACG CAGAACTTGA 720 GCTGCTGCTC CACCCTTCCC ACAAAGCAGG CCTTCCTGCC TGAGCCAGAC TAGAAAAGCC 780 TTCCACAGAA ATGCCACCGC ACCATATAGG GAAGTGCCTG AAGACCTCCC CGCCCCACCT 840 CCAGAATCTG CCAGAATCAG CCCCCTCAGG ATCCTCCATG GCGATGTTGG TTCCTCCCTG 900 GGTCCCCCAG CTGCAGACCA ACACAATGGG GGCTATTCTG GGCTGCACGG GGTATTTAAA 960 GCTCTGACTG GGCCTCCTCC CTGGGGAACA AAAGGCCTTG CCCTCCGTAA GACCTTCCTG 1020 AAATTGTTCC TGCCCAGACT GTGGTGGCTG CATCCTGTAC TGTTCCCCAC CTCCCCTGCC 1080 AGGCCCTGAG GCCCTGTAAG ATTCAGCACA AAATGCCTCC TCCAGGAAGC CCACAGGGCT 1140 GCCTCCTGTG CTCAGCAGCA CTGCCTGAGA CCCTCAGAAA AGCTGGGTCC TGGCTCAACT 1200 CTGCCATCGA TCTTCTCTGG GTCCCAGTTT TCTCATCTGC AAAATATGGA TGTGAATCCC 1260 AGTGTGTGAA AGCACTCCAG AGGCTTCCAT GGTTAGGATG AGTAGTGTCT CTCCAGCCAC 1320 TTTGTGAAGC AGAATATAAG CAGGAACGGG AATTGGTCTG TTTTGTCGCT GCCCTTTTTC 1380 TAGCACCTGG CACACAGTAG GTGCCAAATA AATATTTACT GACTGATACA AATATTTAAA 1440 GAATGTGTCT GTAGCCTCCA TAGAACCACC CAGAATGCCA GGCACACAGG TGGTTAATAC 1500 CCTCGATGGT AACGTTGCCA GCTCTCAGCT TGAGCACAAA GAACACATCA AGCCTTATGC 1560 TAAGTACCTG ATGTTAATTA TCTGATTTAA TTTGCTCAAC AGTCCCAAGA GGTCGGTACC 1620 ATTATCTTAT TTCACAAGCA AGAAAACGGG AGTTCCAGTC CAGGTGGTTA AGCAGCTCGC 1680 CTGAGGTCGC AAATGGCCAA GCTGGGAGTC AAGCCCAGGA GCCCTGAAGC CCCTGGCATC 1740 CTGCGCCAAA TGCACATTGA AGAAAGGCAG TCGGAGAGCA CTGGGTGGGG AGCCAGGAGC 1800 CTGAAGTCAG CCACTAAGCT GTGTGACTTC AAGCAAGTTG CTTGGCCTCT CTGAATCAGT 1860 TTTCTCTTCC ATAAAAACAA GGGCATGAAT TCCTCTTCTT CAGGTCGTTG GTAGGATCAA 1920 AGGAACCAAA GATGTGACTC TGTCTCCCAC ACTAGCCCCA GCCCCTCCCC AAGGGCAGCA 1980 GCTGTGAAGG ATGGTGGGAA GATGTACTGG GAGGAGGGGG CTACCCAGAG CTGGCCCCAG 2040 AACAAAGCTC CACAGCTGCT GACAACAGCT GGGGAGAGCT CTGGGCCTGG CCCAAGCAGG 2100 GGGAGAATGG GCAGGCTGGG AAGTCACCTC TGGCCCTCCT CTGTCACCCT TCCCTGCTGA 2160 CAGCTGCTGA GGCCTCAGGG CCAAGGGCCC 2190
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