| Tag | Content |
|---|
EnhancerAtlas ID | HS059-00597 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:21660340-21663250 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:21661045-21661063 | GGAAGCGAGGGAGGCAGG | + | 6.22 |
|
| | Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
| SE_00105 | chr1:21656775-21671990 | Adipose_Nuclei | | SE_00854 | chr1:21660236-21662991 | Adrenal_Gland | | SE_01643 | chr1:21660262-21662754 | Aorta | | SE_02944 | chr1:21660560-21662580 | Bladder | | SE_03598 | chr1:21660541-21661932 | Brain_Angular_Gyrus | | SE_04518 | chr1:21660215-21662707 | Brain_Anterior_Caudate | | SE_05710 | chr1:21660439-21662968 | Brain_Cingulate_Gyrus | | SE_05944 | chr1:21659989-21673592 | Brain_Hippocampus_Middle | | SE_08398 | chr1:21660398-21662710 | Brain_Inferior_Temporal_Lobe | | SE_08982 | chr1:21661732-21662044 | Brain_Mid_Frontal_Lobe | | SE_26127 | chr1:21660172-21662296 | Duodenum_Smooth_Muscle | | SE_26770 | chr1:21660268-21662706 | Esophagus | | SE_28486 | chr1:21660184-21661733 | Fetal_Intestine | | SE_29337 | chr1:21660165-21661628 | Fetal_Intestine_Large | | SE_31433 | chr1:21660241-21662714 | Gastric | | SE_42174 | chr1:21660216-21662835 | Lung | | SE_44380 | chr1:21660201-21662771 | NHDF-Ad | | SE_45045 | chr1:21660317-21662260 | NHLF | | SE_46660 | chr1:21660404-21662544 | Ovary | | SE_47592 | chr1:21660300-21662327 | Pancreas | | SE_48583 | chr1:21660227-21662766 | Right_Atrium | | SE_50108 | chr1:21660245-21662740 | Sigmoid_Colon | | SE_52633 | chr1:21660234-21662726 | Small_Intestine | | SE_53334 | chr1:21659249-21662815 | Spleen | | SE_54639 | chr1:21660115-21662959 | Stomach_Smooth_Muscle | | SE_56171 | chr1:21660198-21662906 | u87 | | SE_65263 | chr1:21660486-21671744 | Pancreatic_islets | | SE_67931 | chr1:21660198-21662906 | u87 | | SE_68932 | chr1:21660639-21662409 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 21660622 | 21661187 | | chr1 | 21661800 | 21662962 |
|
Enhancer Sequence | GACGGAGCCA CAAAGGTAAT AACAGCTCCC ACCTCCCAAG GGCCAACTCC GTGCACCGTC 60
CTGTGAGCTT TACAACCTGT CATAAATTAT CAACCACTTT TCACAACACC ACTATGAGAA 120
AGGTGCTACC ATCATCCCAT TTCATAGAGG AGAAAACCGA GGCTCAGAGA TGGTCACTCA 180
CCAAAGGTCA CCCAGCTGGG ACTAAGTGAC AGAGCTGGGA CTACAACCCA CATCTGTCTG 240
GCTCCAAAAC CTCCATACCT CCATCTTATC TAGAAAGAGT GCTGGATGAG GAGTCTAGAA 300
TCAGGGTCTA AGTCCTGCCT CTAACCTGCT GTATAGCCTC AGGTAAGTCT CTTTCCCTTT 360
GTGAGCCTTG GTCTGCCCTA TGAGGAAGTT GGCCTAGATG ACCTCCAAGT CCCACCTCCT 420
GTGACTCTGT GAGCTCTCAT GCCCTCCTCT CTCTGGCTCC CAGCCACCAC ACCGGAAGCC 480
CAACAGGATG CCGAGTAACC ACCCACTGAA CACTCAGGGG CGAAGGAAGA TGAAGTGCCG 540
CTTTCTCATG GCCATCTTCC ACCAGACCAG CCCAGGAAAC AAGGAACCAC AAAGCCACAG 600
GATTCCCTCC AGCGTGGCCG TGTGAACAGC AGCCCTGGAG CAGAGGGGCT GGGCATCCCC 660
TTGCGGCCAT CACTTCCTAT GCCCTCACTT CTCGGCAGGG TGTGCGGAAG CGAGGGAGGC 720
AGGCTCCAGC TCAATGCCCT CTGGCTCTGT TTCTCTGGGT CCCCAGGGGC TGGGACGGTG 780
GGAACTGGTC ACTCTGGGAG AATCCCAAGC CCACCCCGGA AGGCTGAGTT GAAGTGGAGG 840
TTCAGACAGG TCTGTCTGGC TCCACAGGTA ACTTTTGCCC ACTGTGCTCT GCTGCCAGCA 900
AGGTCTCGAA GCATCTGGGA TGCCTGGCTA CCTCTCTCCC ATCCCTGAAG TAGCAGCCAA 960
AATCCCAGAT CCTGCAGAAA CCTACGCCTC CTCAGCCTCA GGACAGACGA ATATCCTGAG 1020
GCCCGCGCTC CTGCCTCCCT CCTGCCCCCT ACAGTCCATG CTCTACACAG CAGCCAAGGT 1080
CTTTCCAAAC AGAAACCAAG CCCAGTCGCC CCTCAACGTG GGGTCCTCCA GTGGCTTCCC 1140
ACCACTATTA GAACGAAATG CTGACCCCTG CCCCACAGAC AAGGCTGTCC ATGGCTTGCC 1200
CCTCCAGGCC CACCTCTCCC TAGCCTTCCC TCCACCCTCC ACTGCCTCTG CCCGGCCACA 1260
CCAGCGTTCA CCCCCTACAT GTGCCAAACT TGCTGTTCCG GCAGCCGGGA ACTCTCATCT 1320
CCCCCGCCCC CGTCTTTGCC CGGCTGCCCC CTCCTCAACC TTCATGTCCC AGCTCAGACA 1380
TCACCTCCTT TCCTGGCCGC TCCTCTAGAG CGGCCCCCTC CCCTCACAGC CACTCTCCAC 1440
CACATCGCCC TGTTTTGTCT CCTTTCTTCT CTCGGAGCGA TCCTTCTGGT GGGTGGCTTT 1500
GCCTGTTTGG TCTCCAGCTT CCTCCCCTAG AGTGCAGCTC CTTAGGGGCA GGCATGTGAC 1560
TGCTCCATTC TCTTCTGTCC CCACAATGAG GCAGGGCCTC CTTGGGTGCT CACAACCCTG 1620
AAGATGAGGA CGCTGCAGCC CTGAGAGGTG GATTGAGCCG CCCAAAGTCC CAGAGCCAGG 1680
GAATAGCAGG GTTCAGACCG AGGGCGACCT GATGCCAAGC CTCAGTGGGT GGGGGGCTCT 1740
CACGGCTGGG GGCCTACTCT GGAGGGCTCT CACCCAGGGT GGACAGAGTC GCAGTGAGGC 1800
TCTTAGGGCG GGTACCAAGA ATGAAGGGCC CACCAGCTTT CCCAAATGGT CCTTCTGCAA 1860
GCTACAGGCC AGCTGAGCTC CTGCCTGGGG TGGGTGAGAC CCTGGGGGTG AAGAGGCACC 1920
AAACACCAGG AGCAAAGGCT CCCAAATGAG GGAGACCACA GACACAGGGA GCTGGGAAGC 1980
TTCGACCCAC CCAGTGCTTG ACGGAAGGGG AAAGTGAGGA CTATGGAGGG GAAGGGACTT 2040
GCCTGAGGTC ACACAGCCAA TCAGTGGGTC TCCAGGGAGG GAGGCCCTTC CCTACCCTGC 2100
AGAACAGCAG GCGAAGCCCA AAGCCCAGGG TCTGGGCAGA GTGCCAGCCC AGAACTGCCA 2160
GGCCCTGGGG GCAGGGGCAG GGCTACAGAG TGAATCTGGG GCATTAAGAC AAAGAAAGGA 2220
CTCAAATTTC TTCCTTCTTT CAAAAAACAC TTGAGACAGG CAGTGTCTCA TACCTGTAAT 2280
CCCAGCACCA TGGAAGGCTA AGGTGGATGA ATCACTTGAG CCCAGGAGTT CAATACCAGC 2340
CTTGGCAACT AGTGAGACCT TGTCTCTACA AAAAAATATC AGAAAATTAG CTGGGTGTAG 2400
TGGTGCACCT GTGGTACCAG CTACTCAGGA GGCTGAGGTG GGAAGATCAC TTGAGCCCAT 2460
AAGTTCAAGG CTGCAGTGAG CTGTGTTCAT GCCACTGTAC TCCAGCCTGG GTGACAGAGT 2520
GAGAGACCCT GTCTCAAAAC CAAAACAACA AAAAACATTC ACTGAGGCCG GGCGTGGTGG 2580
CTCACACCTG TAATCCCAGC ACTTTGGGAG GACGAGGTGG GCAGATCACC TGAGGTCAGG 2640
AGTTCGAGAC CAGGCTGGCC AACATGGTGA AACCCCGTCT CTACTAAAAA TACAAAAAAT 2700
TAGTCGGCTG TGGCCGGGCG CGGTGGCTCA CACCTGTAGT AATCCCAGCA CTTTCGGAGG 2760
CCGAGGTGGG CGGATCACGA GGTCAGGAGA TTGAGACCAT CCTGGCTAAC ACAGTGAAAC 2820
CCTGTCTCAA CTAAAAATAC AAAAAATTAG CCAAGCGTGG TGGCGGGCAC CTGTAGTCCC 2880
AGCTACTCAG GAGGCTGAGG CAGGAGAATG 2910
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