Tag | Content |
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EnhancerAtlas ID | HS031-00211 |
Organism | Homo sapiens |
Tissue/cell | Denditric_cell |
Coordinate | chr1:22235450-22237970 |
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 | ATTAGCCGGG CATGGTGGCA CATGCCTGTA ATCCCAGCTA CTTGGGAGGC TGAGGCAGGA 60 GAATCGCTTG AACCCGGGAG GTGGAGGTTG CAGTGGGCCA AGATGGCGCC ATTGCACTCC 120 AGCCTGGGCG ACAGAGTGAG ACTCCATCTC AAAAAACAAA AACAGAAACA ATGTCAGGAC 180 AGAGCCAGAA GGAGTCAGGC TGCAGAGACC CGCTGAGCAA AGGGTCATCA TCACCATCAT 240 CCTCATCATT CATTTATACC TCCCCTCTTG CCCTGTTCCA AAAAGGCTGC AGACAGCTTA 300 CAAAGATGCA CACTTAACAG CCAAGAGAAT ATTAACTAAA GAAATATAAG AAAAACTCAG 360 GCAGGGCAGG CAGATGGAGC CTGGAGTGAG GCAAGCAGAC AGAGAGCACA TGCTGAATCC 420 CAGAGATCTA GGAAAGGGAC AACTCATGTG GCCCTGAGCT TGCCAGCAGC CAATGGGAAG 480 AAGGAAACCT GACCAGTCCC TAGATTCCAT GTCTCACAAT GTAAAAACAA ACCAGTTGCT 540 TAGAAAAAGC ACAACTATCC CTGATACTGA GAGCAGGGAA TGTCCCAAGG GACAGGCTTG 600 TCTGGCACCC TTCTCTGCCT CATCAGTGGG GCTGGCATCC CCTCAGAGTC TGCTGACCAT 660 GACCCTTTGA AGCTGAAGCC AGGGGCAGAG GCTACAGTGA TCAAAGATTC AGGGAGCTGG 720 AATGGCAGTC CAGTCAGTAC CCCACCAACC TCACCCCAGC AGCCTTGGTC TAGGCAGGAT 780 TACCCATCAC TCCCCAAACC CGAACACAGC CAGTGCCCAA AATAGCTAGA GCAGGAGAGG 840 GTGCCAAGAG GCCCTGGCAA GGGCCTGGGC TAGGCCCACC TACAGGAGGG CCCAGTGGGC 900 CAATGCACAC ATACCTCTGG TGCACAAAGA GGCACCTTCA GTCAGGCACA GAGCCGTCCC 960 TGGGAGTCCC CCACCCACCA GGCTCCCCCC TCAGCTGCAC GTTGCTCACG CAGAACTTGA 1020 GCTGCTGCTC CACCCTTCCC ACAAAGCAGG CCTTCCTGCC TGAGCCAGAC TAGAAAAGCC 1080 TTCCACAGAA ATGCCACCGC ACCATATAGG GAAGTGCCTG AAGACCTCCC CGCCCCACCT 1140 CCAGAATCTG CCAGAATCAG CCCCCTCAGG ATCCTCCATG GCGATGTTGG TTCCTCCCTG 1200 GGTCCCCCAG CTGCAGACCA ACACAATGGG GGCTATTCTG GGCTGCACGG GGTATTTAAA 1260 GCTCTGACTG GGCCTCCTCC CTGGGGAACA AAAGGCCTTG CCCTCCGTAA GACCTTCCTG 1320 AAATTGTTCC TGCCCAGACT GTGGTGGCTG CATCCTGTAC TGTTCCCCAC CTCCCCTGCC 1380 AGGCCCTGAG GCCCTGTAAG ATTCAGCACA AAATGCCTCC TCCAGGAAGC CCACAGGGCT 1440 GCCTCCTGTG CTCAGCAGCA CTGCCTGAGA CCCTCAGAAA AGCTGGGTCC TGGCTCAACT 1500 CTGCCATCGA TCTTCTCTGG GTCCCAGTTT TCTCATCTGC AAAATATGGA TGTGAATCCC 1560 AGTGTGTGAA AGCACTCCAG AGGCTTCCAT GGTTAGGATG AGTAGTGTCT CTCCAGCCAC 1620 TTTGTGAAGC AGAATATAAG CAGGAACGGG AATTGGTCTG TTTTGTCGCT GCCCTTTTTC 1680 TAGCACCTGG CACACAGTAG GTGCCAAATA AATATTTACT GACTGATACA AATATTTAAA 1740 GAATGTGTCT GTAGCCTCCA TAGAACCACC CAGAATGCCA GGCACACAGG TGGTTAATAC 1800 CCTCGATGGT AACGTTGCCA GCTCTCAGCT TGAGCACAAA GAACACATCA AGCCTTATGC 1860 TAAGTACCTG ATGTTAATTA TCTGATTTAA TTTGCTCAAC AGTCCCAAGA GGTCGGTACC 1920 ATTATCTTAT TTCACAAGCA AGAAAACGGG AGTTCCAGTC CAGGTGGTTA AGCAGCTCGC 1980 CTGAGGTCGC AAATGGCCAA GCTGGGAGTC AAGCCCAGGA GCCCTGAAGC CCCTGGCATC 2040 CTGCGCCAAA TGCACATTGA AGAAAGGCAG TCGGAGAGCA CTGGGTGGGG AGCCAGGAGC 2100 CTGAAGTCAG CCACTAAGCT GTGTGACTTC AAGCAAGTTG CTTGGCCTCT CTGAATCAGT 2160 TTTCTCTTCC ATAAAAACAA GGGCATGAAT TCCTCTTCTT CAGGTCGTTG GTAGGATCAA 2220 AGGAACCAAA GATGTGACTC TGTCTCCCAC ACTAGCCCCA GCCCCTCCCC AAGGGCAGCA 2280 GCTGTGAAGG ATGGTGGGAA GATGTACTGG GAGGAGGGGG CTACCCAGAG CTGGCCCCAG 2340 AACAAAGCTC CACAGCTGCT GACAACAGCT GGGGAGAGCT CTGGGCCTGG CCCAAGCAGG 2400 GGGAGAATGG GCAGGCTGGG AAGTCACCTC TGGCCCTCCT CTGTCACCCT TCCCTGCTGA 2460 CAGCTGCTGA GGCCTCAGGG CCAAGGGCCC CAGAGCAGGC AGGGAGTGGG GGTGTGGAGG 2520
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