| Tag | Content |
|---|
EnhancerAtlas ID | HS047-00480 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:21660400-21663100 |
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 | CTGTGAGCTT TACAACCTGT CATAAATTAT CAACCACTTT TCACAACACC ACTATGAGAA 60
AGGTGCTACC ATCATCCCAT TTCATAGAGG AGAAAACCGA GGCTCAGAGA TGGTCACTCA 120
CCAAAGGTCA CCCAGCTGGG ACTAAGTGAC AGAGCTGGGA CTACAACCCA CATCTGTCTG 180
GCTCCAAAAC CTCCATACCT CCATCTTATC TAGAAAGAGT GCTGGATGAG GAGTCTAGAA 240
TCAGGGTCTA AGTCCTGCCT CTAACCTGCT GTATAGCCTC AGGTAAGTCT CTTTCCCTTT 300
GTGAGCCTTG GTCTGCCCTA TGAGGAAGTT GGCCTAGATG ACCTCCAAGT CCCACCTCCT 360
GTGACTCTGT GAGCTCTCAT GCCCTCCTCT CTCTGGCTCC CAGCCACCAC ACCGGAAGCC 420
CAACAGGATG CCGAGTAACC ACCCACTGAA CACTCAGGGG CGAAGGAAGA TGAAGTGCCG 480
CTTTCTCATG GCCATCTTCC ACCAGACCAG CCCAGGAAAC AAGGAACCAC AAAGCCACAG 540
GATTCCCTCC AGCGTGGCCG TGTGAACAGC AGCCCTGGAG CAGAGGGGCT GGGCATCCCC 600
TTGCGGCCAT CACTTCCTAT GCCCTCACTT CTCGGCAGGG TGTGCGGAAG CGAGGGAGGC 660
AGGCTCCAGC TCAATGCCCT CTGGCTCTGT TTCTCTGGGT CCCCAGGGGC TGGGACGGTG 720
GGAACTGGTC ACTCTGGGAG AATCCCAAGC CCACCCCGGA AGGCTGAGTT GAAGTGGAGG 780
TTCAGACAGG TCTGTCTGGC TCCACAGGTA ACTTTTGCCC ACTGTGCTCT GCTGCCAGCA 840
AGGTCTCGAA GCATCTGGGA TGCCTGGCTA CCTCTCTCCC ATCCCTGAAG TAGCAGCCAA 900
AATCCCAGAT CCTGCAGAAA CCTACGCCTC CTCAGCCTCA GGACAGACGA ATATCCTGAG 960
GCCCGCGCTC CTGCCTCCCT CCTGCCCCCT ACAGTCCATG CTCTACACAG CAGCCAAGGT 1020
CTTTCCAAAC AGAAACCAAG CCCAGTCGCC CCTCAACGTG GGGTCCTCCA GTGGCTTCCC 1080
ACCACTATTA GAACGAAATG CTGACCCCTG CCCCACAGAC AAGGCTGTCC ATGGCTTGCC 1140
CCTCCAGGCC CACCTCTCCC TAGCCTTCCC TCCACCCTCC ACTGCCTCTG CCCGGCCACA 1200
CCAGCGTTCA CCCCCTACAT GTGCCAAACT TGCTGTTCCG GCAGCCGGGA ACTCTCATCT 1260
CCCCCGCCCC CGTCTTTGCC CGGCTGCCCC CTCCTCAACC TTCATGTCCC AGCTCAGACA 1320
TCACCTCCTT TCCTGGCCGC TCCTCTAGAG CGGCCCCCTC CCCTCACAGC CACTCTCCAC 1380
CACATCGCCC TGTTTTGTCT CCTTTCTTCT CTCGGAGCGA TCCTTCTGGT GGGTGGCTTT 1440
GCCTGTTTGG TCTCCAGCTT CCTCCCCTAG AGTGCAGCTC CTTAGGGGCA GGCATGTGAC 1500
TGCTCCATTC TCTTCTGTCC CCACAATGAG GCAGGGCCTC CTTGGGTGCT CACAACCCTG 1560
AAGATGAGGA CGCTGCAGCC CTGAGAGGTG GATTGAGCCG CCCAAAGTCC CAGAGCCAGG 1620
GAATAGCAGG GTTCAGACCG AGGGCGACCT GATGCCAAGC CTCAGTGGGT GGGGGGCTCT 1680
CACGGCTGGG GGCCTACTCT GGAGGGCTCT CACCCAGGGT GGACAGAGTC GCAGTGAGGC 1740
TCTTAGGGCG GGTACCAAGA ATGAAGGGCC CACCAGCTTT CCCAAATGGT CCTTCTGCAA 1800
GCTACAGGCC AGCTGAGCTC CTGCCTGGGG TGGGTGAGAC CCTGGGGGTG AAGAGGCACC 1860
AAACACCAGG AGCAAAGGCT CCCAAATGAG GGAGACCACA GACACAGGGA GCTGGGAAGC 1920
TTCGACCCAC CCAGTGCTTG ACGGAAGGGG AAAGTGAGGA CTATGGAGGG GAAGGGACTT 1980
GCCTGAGGTC ACACAGCCAA TCAGTGGGTC TCCAGGGAGG GAGGCCCTTC CCTACCCTGC 2040
AGAACAGCAG GCGAAGCCCA AAGCCCAGGG TCTGGGCAGA GTGCCAGCCC AGAACTGCCA 2100
GGCCCTGGGG GCAGGGGCAG GGCTACAGAG TGAATCTGGG GCATTAAGAC AAAGAAAGGA 2160
CTCAAATTTC TTCCTTCTTT CAAAAAACAC TTGAGACAGG CAGTGTCTCA TACCTGTAAT 2220
CCCAGCACCA TGGAAGGCTA AGGTGGATGA ATCACTTGAG CCCAGGAGTT CAATACCAGC 2280
CTTGGCAACT AGTGAGACCT TGTCTCTACA AAAAAATATC AGAAAATTAG CTGGGTGTAG 2340
TGGTGCACCT GTGGTACCAG CTACTCAGGA GGCTGAGGTG GGAAGATCAC TTGAGCCCAT 2400
AAGTTCAAGG CTGCAGTGAG CTGTGTTCAT GCCACTGTAC TCCAGCCTGG GTGACAGAGT 2460
GAGAGACCCT GTCTCAAAAC CAAAACAACA AAAAACATTC ACTGAGGCCG GGCGTGGTGG 2520
CTCACACCTG TAATCCCAGC ACTTTGGGAG GACGAGGTGG GCAGATCACC TGAGGTCAGG 2580
AGTTCGAGAC CAGGCTGGCC AACATGGTGA AACCCCGTCT CTACTAAAAA TACAAAAAAT 2640
TAGTCGGCTG TGGCCGGGCG CGGTGGCTCA CACCTGTAGT AATCCCAGCA CTTTCGGAGG 2700
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