| Tag | Content |
|---|
EnhancerAtlas ID | HS059-00623 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:22235760-22238290 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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 |
|
| | Number of super-enhancer constituents: 41 | 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_02999 | chr1:22237999-22239189 | Bladder | | SE_06476 | chr1:22235474-22238889 | Brain_Hippocampus_Middle | | SE_13865 | chr1:22227437-22237425 | CD34_Primary_RO01536 | | SE_13865 | chr1:22237959-22239034 | 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 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I021893 | chr1 | 22220486 | 22243088 |
|
Enhancer Sequence | CACTTAACAG CCAAGAGAAT ATTAACTAAA GAAATATAAG AAAAACTCAG GCAGGGCAGG 60
CAGATGGAGC CTGGAGTGAG GCAAGCAGAC AGAGAGCACA TGCTGAATCC CAGAGATCTA 120
GGAAAGGGAC AACTCATGTG GCCCTGAGCT TGCCAGCAGC CAATGGGAAG AAGGAAACCT 180
GACCAGTCCC TAGATTCCAT GTCTCACAAT GTAAAAACAA ACCAGTTGCT TAGAAAAAGC 240
ACAACTATCC CTGATACTGA GAGCAGGGAA TGTCCCAAGG GACAGGCTTG TCTGGCACCC 300
TTCTCTGCCT CATCAGTGGG GCTGGCATCC CCTCAGAGTC TGCTGACCAT GACCCTTTGA 360
AGCTGAAGCC AGGGGCAGAG GCTACAGTGA TCAAAGATTC AGGGAGCTGG AATGGCAGTC 420
CAGTCAGTAC CCCACCAACC TCACCCCAGC AGCCTTGGTC TAGGCAGGAT TACCCATCAC 480
TCCCCAAACC CGAACACAGC CAGTGCCCAA AATAGCTAGA GCAGGAGAGG GTGCCAAGAG 540
GCCCTGGCAA GGGCCTGGGC TAGGCCCACC TACAGGAGGG CCCAGTGGGC CAATGCACAC 600
ATACCTCTGG TGCACAAAGA GGCACCTTCA GTCAGGCACA GAGCCGTCCC TGGGAGTCCC 660
CCACCCACCA GGCTCCCCCC TCAGCTGCAC GTTGCTCACG CAGAACTTGA GCTGCTGCTC 720
CACCCTTCCC ACAAAGCAGG CCTTCCTGCC TGAGCCAGAC TAGAAAAGCC TTCCACAGAA 780
ATGCCACCGC ACCATATAGG GAAGTGCCTG AAGACCTCCC CGCCCCACCT CCAGAATCTG 840
CCAGAATCAG CCCCCTCAGG ATCCTCCATG GCGATGTTGG TTCCTCCCTG GGTCCCCCAG 900
CTGCAGACCA ACACAATGGG GGCTATTCTG GGCTGCACGG GGTATTTAAA GCTCTGACTG 960
GGCCTCCTCC CTGGGGAACA AAAGGCCTTG CCCTCCGTAA GACCTTCCTG AAATTGTTCC 1020
TGCCCAGACT GTGGTGGCTG CATCCTGTAC TGTTCCCCAC CTCCCCTGCC AGGCCCTGAG 1080
GCCCTGTAAG ATTCAGCACA AAATGCCTCC TCCAGGAAGC CCACAGGGCT GCCTCCTGTG 1140
CTCAGCAGCA CTGCCTGAGA CCCTCAGAAA AGCTGGGTCC TGGCTCAACT CTGCCATCGA 1200
TCTTCTCTGG GTCCCAGTTT TCTCATCTGC AAAATATGGA TGTGAATCCC AGTGTGTGAA 1260
AGCACTCCAG AGGCTTCCAT GGTTAGGATG AGTAGTGTCT CTCCAGCCAC TTTGTGAAGC 1320
AGAATATAAG CAGGAACGGG AATTGGTCTG TTTTGTCGCT GCCCTTTTTC TAGCACCTGG 1380
CACACAGTAG GTGCCAAATA AATATTTACT GACTGATACA AATATTTAAA GAATGTGTCT 1440
GTAGCCTCCA TAGAACCACC CAGAATGCCA GGCACACAGG TGGTTAATAC CCTCGATGGT 1500
AACGTTGCCA GCTCTCAGCT TGAGCACAAA GAACACATCA AGCCTTATGC TAAGTACCTG 1560
ATGTTAATTA TCTGATTTAA TTTGCTCAAC AGTCCCAAGA GGTCGGTACC ATTATCTTAT 1620
TTCACAAGCA AGAAAACGGG AGTTCCAGTC CAGGTGGTTA AGCAGCTCGC CTGAGGTCGC 1680
AAATGGCCAA GCTGGGAGTC AAGCCCAGGA GCCCTGAAGC CCCTGGCATC CTGCGCCAAA 1740
TGCACATTGA AGAAAGGCAG TCGGAGAGCA CTGGGTGGGG AGCCAGGAGC CTGAAGTCAG 1800
CCACTAAGCT GTGTGACTTC AAGCAAGTTG CTTGGCCTCT CTGAATCAGT TTTCTCTTCC 1860
ATAAAAACAA GGGCATGAAT TCCTCTTCTT CAGGTCGTTG GTAGGATCAA AGGAACCAAA 1920
GATGTGACTC TGTCTCCCAC ACTAGCCCCA GCCCCTCCCC AAGGGCAGCA GCTGTGAAGG 1980
ATGGTGGGAA GATGTACTGG GAGGAGGGGG CTACCCAGAG CTGGCCCCAG AACAAAGCTC 2040
CACAGCTGCT GACAACAGCT GGGGAGAGCT CTGGGCCTGG CCCAAGCAGG GGGAGAATGG 2100
GCAGGCTGGG AAGTCACCTC TGGCCCTCCT CTGTCACCCT TCCCTGCTGA CAGCTGCTGA 2160
GGCCTCAGGG CCAAGGGCCC CAGAGCAGGC AGGGAGTGGG GGTGTGGAGG GGGTGGGCGG 2220
GCTGGCTGGG GTCATCTTAG TCCTCATGCT GTCAACTGCT CAAGCCTCAG GGTGCCTGGC 2280
CTCGCTGTCC CATAGCACAG CCCTTTACCC AGTTCCCTGG GAAGCCTGGG TGGAGAGGCC 2340
GGAGCAAAGG TCTGGGGCTG AACATGCCTT AACTGGAGCC TGGCCTGCTC CAGGGCCCCC 2400
GTGGGGAGGT GCAGGGCCGG GAGGGAGGGA GTCCTGAAGA GGCTTGCAAT TTCCCTGGTG 2460
CACAGCCCCA CTGCAGGCCC TTCAGGAAAC GTCCCTGGAG GCTGTGAGCT TGGCCCACCC 2520
CAGCCCATCT 2530
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