| Tag | Content |
|---|
EnhancerAtlas ID | HS026-00497 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr1:21639290-21642040 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BARHL2 | MA0635.1 | chr1:21640493-21640503 | GCTAAACGGT | + | 6.02 | | MEF2B | MA0660.1 | chr1:21639333-21639345 | GCTAATAATAGC | + | 6.07 | | MIXL1 | MA0662.1 | chr1:21640589-21640599 | TCTAATTAAC | + | 6.02 |
|
| | Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
| SE_00105 | chr1:21640019-21654616 | Adipose_Nuclei | | SE_00854 | chr1:21639451-21641453 | Adrenal_Gland | | SE_00854 | chr1:21641602-21642092 | Adrenal_Gland | | SE_01643 | chr1:21639425-21641555 | Aorta | | SE_02944 | chr1:21640912-21641449 | Bladder | | SE_04518 | chr1:21639355-21640025 | Brain_Anterior_Caudate | | SE_05710 | chr1:21639125-21641783 | Brain_Cingulate_Gyrus | | SE_05944 | chr1:21639044-21646536 | Brain_Hippocampus_Middle | | SE_08398 | chr1:21639007-21640675 | Brain_Inferior_Temporal_Lobe | | SE_26127 | chr1:21639824-21641988 | Duodenum_Smooth_Muscle | | SE_26770 | chr1:21639500-21641528 | Esophagus | | SE_28486 | chr1:21639904-21640821 | Fetal_Intestine | | SE_31433 | chr1:21639359-21640599 | Gastric | | SE_31433 | chr1:21640646-21641344 | Gastric | | SE_42174 | chr1:21639360-21640363 | Lung | | SE_44380 | chr1:21639052-21642110 | NHDF-Ad | | SE_45045 | chr1:21639124-21641481 | NHLF | | SE_46660 | chr1:21639608-21640018 | Ovary | | SE_46660 | chr1:21640643-21641290 | Ovary | | SE_47592 | chr1:21639448-21639851 | Pancreas | | SE_48583 | chr1:21639382-21641534 | Right_Atrium | | SE_50108 | chr1:21639410-21641515 | Sigmoid_Colon | | SE_54639 | chr1:21639148-21648300 | Stomach_Smooth_Muscle | | SE_56171 | chr1:21639209-21642705 | u87 | | SE_65263 | chr1:21639302-21641232 | Pancreatic_islets | | SE_67931 | chr1:21639209-21642705 | u87 | | SE_68932 | chr1:21639403-21641393 | 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 |
| GH01I021312 | chr1 | 21638973 | 21657659 |
|
Enhancer Sequence | GATATGACCT CCCTGTGCCT TGGTTTATCA TTAAAAAAAC AAAGCTAATA ATAGCCCCAC 60
TCTCATAGGT AGCTATGAGA ATTAAAATAG TTCAAAGACA CAAAGTATTG TGATCACCAG 120
CACTGCTATT TGATCCTCTC ATGCAGATGT AAGGTAAATA CTATCATTGT CTCTCATTTT 180
GCAGATGCTA AAACTGCAAC TCAGAGAGGG GTAGTGACTT GCTTGGATCA CACAGCCAGA 240
AAGTGACAGG GCAGGACTGG ACACCAGGTC TGTCTGACTC TAAACTACTT ATTGTTTCCA 300
CTCTGCCCTC TGCGCCCCAC TATTCCCTCC TGGACTCTGA TGCCTCTGTG CTTGTCCCCT 360
CACCTGCCCA CAATGCCAAG GCCAACTCCC CTTGTCTAGC CCCAGCCAAT CAGGGTGGAC 420
CTGCAGCCAA ACCAGATGCT GCTGAGCTGG CGTTGCCTCG GTGACCAGGC ATATCTGCTG 480
GACAAGCCCA CCCCAGGCTC AGCTTCCCAT CTGGTCCCCA GTACACTCCA TCCCCCTCAA 540
GACACATGTG TCATGCTTGC CTGGGGGGAT GGAGGGAGCC CGGGAGGAAA CGCCTGGCTG 600
GGGAGAGGAG GGCTGATTCC AGCTGACAGT GGGGGAATGA TGACTGCATT GGCTCAGGAG 660
GACAGGAGCT GCCCTAGCTG CAGTCTTGGT CCAGAGTGGT CCCAGGCCCA GAGCAGAGCT 720
GGGCGGGGAT GAGAACTAGG GAGAGGAATA CATGATGCAG GTGGGAGTGG GGGAGCAGGG 780
GGCTGAGCAC CAGGCTCAGA TCCAATGAGA ACAAGCTGCT CCCTCAACCT TGGAGTGGAA 840
AGAACAAAGG TTCTGGAACA GACAGACCTC AGCTGGACTC TCTGTAATTT ACTGCTGTGT 900
GACCCTGGGT GAGTTGCCTT ACCTCTCTGA GCATGTGTTC TCATCTATAA AATGGGGACA 960
TGTGAACCTA CTTCACTGGG CTATGGTGGG AATTAAGGCG ATAATCCATG AAAAGGCACA 1020
TGGGGAATTC AAGTGCTGCC TCCTAAAGAG AGGCACTGCC AAGGTAATGC CTGTGGCACA 1080
GGAATGTCCC GGCTCACGGA GAACGGGTAC GAGCAGCTGG AATGACCCTG GGTTCAACCT 1140
GAGCAGTAGT GTGGCCTGGG TTACAGATGT AGGGGCAATG ATGACAGTGC TGAGGCTGCA 1200
GCTGCTAAAC GGTAACACCA ACGACATGGC ACCAGCAAAA GCCACATCTT GAGCAATGAC 1260
TTCATTCTAG GTTCCGTGCT AAGCACTTTA CGTGTGTTTT CTAATTAACC ATAACAGCAA 1320
CCCCACGTGA AAGATGTGGA ATAAGAGACA CAGAGAGGTT AAGTAACAAG TCCAAGGTTG 1380
CACAGCTGGT AAAAAGATGG GATCAAATTT GAACCCAATT TCTACCCGAT ACTCAGGCAT 1440
TATGGGAGCC TGCAGAATGG CGTGGGAGTT CTGGGAAGGG GGCGCTGGCT AGGCCCTTCC 1500
TGGGACACTC ACGCAGCCAC ATTCCCAAAC CCCCTCCCGG GCCCCCAAAT TCCTGGCTCG 1560
GTAGTGATAC AGCCTGAGCT CCTCCTCTCC CTCCAGGGCT TGGCTCAGTT CAGTCCCATT 1620
CGGGAGCCAA TCTGCCATTG CACAATTAAC AATTAGGAAC AACTTTTCTT TTCTTCCAAG 1680
GCAGGGATCG GCCCCAGCCC TGGTGACAGG GACACAGTGG GGCTTCTGAC AGAACCTACT 1740
AGGTATGTCC CCAGCCCCTT GCCAAGCTGG GTGACCCCTT TCCTAACCCA GCCCAGTCAG 1800
GAAATCAAGG GTCAGACAGC CCCTCTCCAT CTTCCTTTGT CATCTAAATC CAACCTCCCC 1860
TCCAGGGAAC TTCCTGACTG TCCTGGCTCA CAGCTTTCAC GTGTTCCTAA GACCCCAACG 1920
CCACTGATTC TTTGTCTATT CAGTCAGTAC CTGGCCTGTG CCATTTCCAT GGGATCATGT 1980
ATCTTTATCT ACTGCAAGCA ACTTGAGTTT GTTTGTTGTT GTTTTTGTAA ACAACACTGT 2040
GCTTATCCCT CTCAATACCA AATCTAGTCC AGGACGCATA GAAACTGTTT GACCTATGGT 2100
CTGCTTCTTG GCTTGGAGAA CTCCTATTCA CCCTCCAAAA CCCAGATGAA ATGTCATCTC 2160
CTCTATGAAG TCTTCCTCTG TGTCCCATGC TGCCCCATCT GTATGTATCT GTAGTGATTT 2220
GTATGTATCC CCAGTAGAAA ACCCTCCCTT GTACTGTAAT TAATAACTAC TATCCAGGCA 2280
CTGTGTTAAG ACTGTCACAC TCATTAATTT CAAATCTATC TCTCTGCAAG CCAGAGTCAA 2340
TACCTATTTA ACAGATGGGG GTGATAAGGC TCAGAAAGGT TAAGAGGCTT GCCTAAAATC 2400
ACACAGCTAA TAAGTGGCAG ATCTGTAATT TGAGCCCAGG TCTGCTCATG TCCCAAGCAA 2460
ATAATTCTTT GGTTGGTTCA GGCTGCCACC TCCATCCAAC TGCAGCTGAA TCCGATGCCT 2520
ACTGGGGTCC CAACCTTTGC AGTTCCCCAA TGGATCAACC TCAGAGATGA GCTGTCACTC 2580
AGCCCCAATG TCTGGGGTAT CCCAGGCCAA AGGTGATCTA CCAGCTGGTG CCACCTCACC 2640
CTCACGGCGT CTAGGACAAC CTGGAAAGTC CTAGGGGCTT GTATATAGGC AACTAGGCAT 2700
TAAAAGCTGC TCCTGGCCGG GCATGGGGGC TCAGGTTTGT AGTCCCAGCA 2750
|
