| Tag | Content |
|---|
EnhancerAtlas ID | HS104-00741 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:21660220-21662910 |
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 | 21660291 | 21661228 |
|
Enhancer Sequence | GGAGGCTGAG GCAGGAGAAT TGCTTAAACC CAGGAGGTGG AGGTTGTAGT GAGCTGAGAT 60
CGTGCCACTG CACTCCAATC TGGGCAACAG AGCGAGACTC CGTCTCAAAA AAAAAAAAAT 120
GACGGAGCCA CAAAGGTAAT AACAGCTCCC ACCTCCCAAG GGCCAACTCC GTGCACCGTC 180
CTGTGAGCTT TACAACCTGT CATAAATTAT CAACCACTTT TCACAACACC ACTATGAGAA 240
AGGTGCTACC ATCATCCCAT TTCATAGAGG AGAAAACCGA GGCTCAGAGA TGGTCACTCA 300
CCAAAGGTCA CCCAGCTGGG ACTAAGTGAC AGAGCTGGGA CTACAACCCA CATCTGTCTG 360
GCTCCAAAAC CTCCATACCT CCATCTTATC TAGAAAGAGT GCTGGATGAG GAGTCTAGAA 420
TCAGGGTCTA AGTCCTGCCT CTAACCTGCT GTATAGCCTC AGGTAAGTCT CTTTCCCTTT 480
GTGAGCCTTG GTCTGCCCTA TGAGGAAGTT GGCCTAGATG ACCTCCAAGT CCCACCTCCT 540
GTGACTCTGT GAGCTCTCAT GCCCTCCTCT CTCTGGCTCC CAGCCACCAC ACCGGAAGCC 600
CAACAGGATG CCGAGTAACC ACCCACTGAA CACTCAGGGG CGAAGGAAGA TGAAGTGCCG 660
CTTTCTCATG GCCATCTTCC ACCAGACCAG CCCAGGAAAC AAGGAACCAC AAAGCCACAG 720
GATTCCCTCC AGCGTGGCCG TGTGAACAGC AGCCCTGGAG CAGAGGGGCT GGGCATCCCC 780
TTGCGGCCAT CACTTCCTAT GCCCTCACTT CTCGGCAGGG TGTGCGGAAG CGAGGGAGGC 840
AGGCTCCAGC TCAATGCCCT CTGGCTCTGT TTCTCTGGGT CCCCAGGGGC TGGGACGGTG 900
GGAACTGGTC ACTCTGGGAG AATCCCAAGC CCACCCCGGA AGGCTGAGTT GAAGTGGAGG 960
TTCAGACAGG TCTGTCTGGC TCCACAGGTA ACTTTTGCCC ACTGTGCTCT GCTGCCAGCA 1020
AGGTCTCGAA GCATCTGGGA TGCCTGGCTA CCTCTCTCCC ATCCCTGAAG TAGCAGCCAA 1080
AATCCCAGAT CCTGCAGAAA CCTACGCCTC CTCAGCCTCA GGACAGACGA ATATCCTGAG 1140
GCCCGCGCTC CTGCCTCCCT CCTGCCCCCT ACAGTCCATG CTCTACACAG CAGCCAAGGT 1200
CTTTCCAAAC AGAAACCAAG CCCAGTCGCC CCTCAACGTG GGGTCCTCCA GTGGCTTCCC 1260
ACCACTATTA GAACGAAATG CTGACCCCTG CCCCACAGAC AAGGCTGTCC ATGGCTTGCC 1320
CCTCCAGGCC CACCTCTCCC TAGCCTTCCC TCCACCCTCC ACTGCCTCTG CCCGGCCACA 1380
CCAGCGTTCA CCCCCTACAT GTGCCAAACT TGCTGTTCCG GCAGCCGGGA ACTCTCATCT 1440
CCCCCGCCCC CGTCTTTGCC CGGCTGCCCC CTCCTCAACC TTCATGTCCC AGCTCAGACA 1500
TCACCTCCTT TCCTGGCCGC TCCTCTAGAG CGGCCCCCTC CCCTCACAGC CACTCTCCAC 1560
CACATCGCCC TGTTTTGTCT CCTTTCTTCT CTCGGAGCGA TCCTTCTGGT GGGTGGCTTT 1620
GCCTGTTTGG TCTCCAGCTT CCTCCCCTAG AGTGCAGCTC CTTAGGGGCA GGCATGTGAC 1680
TGCTCCATTC TCTTCTGTCC CCACAATGAG GCAGGGCCTC CTTGGGTGCT CACAACCCTG 1740
AAGATGAGGA CGCTGCAGCC CTGAGAGGTG GATTGAGCCG CCCAAAGTCC CAGAGCCAGG 1800
GAATAGCAGG GTTCAGACCG AGGGCGACCT GATGCCAAGC CTCAGTGGGT GGGGGGCTCT 1860
CACGGCTGGG GGCCTACTCT GGAGGGCTCT CACCCAGGGT GGACAGAGTC GCAGTGAGGC 1920
TCTTAGGGCG GGTACCAAGA ATGAAGGGCC CACCAGCTTT CCCAAATGGT CCTTCTGCAA 1980
GCTACAGGCC AGCTGAGCTC CTGCCTGGGG TGGGTGAGAC CCTGGGGGTG AAGAGGCACC 2040
AAACACCAGG AGCAAAGGCT CCCAAATGAG GGAGACCACA GACACAGGGA GCTGGGAAGC 2100
TTCGACCCAC CCAGTGCTTG ACGGAAGGGG AAAGTGAGGA CTATGGAGGG GAAGGGACTT 2160
GCCTGAGGTC ACACAGCCAA TCAGTGGGTC TCCAGGGAGG GAGGCCCTTC CCTACCCTGC 2220
AGAACAGCAG GCGAAGCCCA AAGCCCAGGG TCTGGGCAGA GTGCCAGCCC AGAACTGCCA 2280
GGCCCTGGGG GCAGGGGCAG GGCTACAGAG TGAATCTGGG GCATTAAGAC AAAGAAAGGA 2340
CTCAAATTTC TTCCTTCTTT CAAAAAACAC TTGAGACAGG CAGTGTCTCA TACCTGTAAT 2400
CCCAGCACCA TGGAAGGCTA AGGTGGATGA ATCACTTGAG CCCAGGAGTT CAATACCAGC 2460
CTTGGCAACT AGTGAGACCT TGTCTCTACA AAAAAATATC AGAAAATTAG CTGGGTGTAG 2520
TGGTGCACCT GTGGTACCAG CTACTCAGGA GGCTGAGGTG GGAAGATCAC TTGAGCCCAT 2580
AAGTTCAAGG CTGCAGTGAG CTGTGTTCAT GCCACTGTAC TCCAGCCTGG GTGACAGAGT 2640
GAGAGACCCT GTCTCAAAAC CAAAACAACA AAAAACATTC ACTGAGGCCG 2690
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