| Tag | Content |
|---|
EnhancerAtlas ID | HS034-00578 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr1:22235820-22238360 |
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 | CAGATGGAGC CTGGAGTGAG GCAAGCAGAC AGAGAGCACA TGCTGAATCC CAGAGATCTA 60
GGAAAGGGAC AACTCATGTG GCCCTGAGCT TGCCAGCAGC CAATGGGAAG AAGGAAACCT 120
GACCAGTCCC TAGATTCCAT GTCTCACAAT GTAAAAACAA ACCAGTTGCT TAGAAAAAGC 180
ACAACTATCC CTGATACTGA GAGCAGGGAA TGTCCCAAGG GACAGGCTTG TCTGGCACCC 240
TTCTCTGCCT CATCAGTGGG GCTGGCATCC CCTCAGAGTC TGCTGACCAT GACCCTTTGA 300
AGCTGAAGCC AGGGGCAGAG GCTACAGTGA TCAAAGATTC AGGGAGCTGG AATGGCAGTC 360
CAGTCAGTAC CCCACCAACC TCACCCCAGC AGCCTTGGTC TAGGCAGGAT TACCCATCAC 420
TCCCCAAACC CGAACACAGC CAGTGCCCAA AATAGCTAGA GCAGGAGAGG GTGCCAAGAG 480
GCCCTGGCAA GGGCCTGGGC TAGGCCCACC TACAGGAGGG CCCAGTGGGC CAATGCACAC 540
ATACCTCTGG TGCACAAAGA GGCACCTTCA GTCAGGCACA GAGCCGTCCC TGGGAGTCCC 600
CCACCCACCA GGCTCCCCCC TCAGCTGCAC GTTGCTCACG CAGAACTTGA GCTGCTGCTC 660
CACCCTTCCC ACAAAGCAGG CCTTCCTGCC TGAGCCAGAC TAGAAAAGCC TTCCACAGAA 720
ATGCCACCGC ACCATATAGG GAAGTGCCTG AAGACCTCCC CGCCCCACCT CCAGAATCTG 780
CCAGAATCAG CCCCCTCAGG ATCCTCCATG GCGATGTTGG TTCCTCCCTG GGTCCCCCAG 840
CTGCAGACCA ACACAATGGG GGCTATTCTG GGCTGCACGG GGTATTTAAA GCTCTGACTG 900
GGCCTCCTCC CTGGGGAACA AAAGGCCTTG CCCTCCGTAA GACCTTCCTG AAATTGTTCC 960
TGCCCAGACT GTGGTGGCTG CATCCTGTAC TGTTCCCCAC CTCCCCTGCC AGGCCCTGAG 1020
GCCCTGTAAG ATTCAGCACA AAATGCCTCC TCCAGGAAGC CCACAGGGCT GCCTCCTGTG 1080
CTCAGCAGCA CTGCCTGAGA CCCTCAGAAA AGCTGGGTCC TGGCTCAACT CTGCCATCGA 1140
TCTTCTCTGG GTCCCAGTTT TCTCATCTGC AAAATATGGA TGTGAATCCC AGTGTGTGAA 1200
AGCACTCCAG AGGCTTCCAT GGTTAGGATG AGTAGTGTCT CTCCAGCCAC TTTGTGAAGC 1260
AGAATATAAG CAGGAACGGG AATTGGTCTG TTTTGTCGCT GCCCTTTTTC TAGCACCTGG 1320
CACACAGTAG GTGCCAAATA AATATTTACT GACTGATACA AATATTTAAA GAATGTGTCT 1380
GTAGCCTCCA TAGAACCACC CAGAATGCCA GGCACACAGG TGGTTAATAC CCTCGATGGT 1440
AACGTTGCCA GCTCTCAGCT TGAGCACAAA GAACACATCA AGCCTTATGC TAAGTACCTG 1500
ATGTTAATTA TCTGATTTAA TTTGCTCAAC AGTCCCAAGA GGTCGGTACC ATTATCTTAT 1560
TTCACAAGCA AGAAAACGGG AGTTCCAGTC CAGGTGGTTA AGCAGCTCGC CTGAGGTCGC 1620
AAATGGCCAA GCTGGGAGTC AAGCCCAGGA GCCCTGAAGC CCCTGGCATC CTGCGCCAAA 1680
TGCACATTGA AGAAAGGCAG TCGGAGAGCA CTGGGTGGGG AGCCAGGAGC CTGAAGTCAG 1740
CCACTAAGCT GTGTGACTTC AAGCAAGTTG CTTGGCCTCT CTGAATCAGT TTTCTCTTCC 1800
ATAAAAACAA GGGCATGAAT TCCTCTTCTT CAGGTCGTTG GTAGGATCAA AGGAACCAAA 1860
GATGTGACTC TGTCTCCCAC ACTAGCCCCA GCCCCTCCCC AAGGGCAGCA GCTGTGAAGG 1920
ATGGTGGGAA GATGTACTGG GAGGAGGGGG CTACCCAGAG CTGGCCCCAG AACAAAGCTC 1980
CACAGCTGCT GACAACAGCT GGGGAGAGCT CTGGGCCTGG CCCAAGCAGG GGGAGAATGG 2040
GCAGGCTGGG AAGTCACCTC TGGCCCTCCT CTGTCACCCT TCCCTGCTGA CAGCTGCTGA 2100
GGCCTCAGGG CCAAGGGCCC CAGAGCAGGC AGGGAGTGGG GGTGTGGAGG GGGTGGGCGG 2160
GCTGGCTGGG GTCATCTTAG TCCTCATGCT GTCAACTGCT CAAGCCTCAG GGTGCCTGGC 2220
CTCGCTGTCC CATAGCACAG CCCTTTACCC AGTTCCCTGG GAAGCCTGGG TGGAGAGGCC 2280
GGAGCAAAGG TCTGGGGCTG AACATGCCTT AACTGGAGCC TGGCCTGCTC CAGGGCCCCC 2340
GTGGGGAGGT GCAGGGCCGG GAGGGAGGGA GTCCTGAAGA GGCTTGCAAT TTCCCTGGTG 2400
CACAGCCCCA CTGCAGGCCC TTCAGGAAAC GTCCCTGGAG GCTGTGAGCT TGGCCCACCC 2460
CAGCCCATCT CAGCCCCCTC AGCTGCCGGC CAGCCCAGCT CCACTCCCAG TTCGGTGCCA 2520
AGCCTTTCCA GCCCGCTCCA 2540
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