| Tag | Content |
|---|
EnhancerAtlas ID | HS091-08315 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:75263680-75266820 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr11:75264004-75264022 | GCTTCCTCCCCTCCGTCC | - | 6.31 | | NFAT5 | MA0606.1 | chr11:75265075-75265085 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr11:75265075-75265085 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr11:75265075-75265085 | AATGGAAAAT | - | 6.02 |
|
| | Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
| SE_00212 | chr11:75264080-75279596 | Adipose_Nuclei | | SE_01033 | chr11:75264881-75266758 | Adrenal_Gland | | SE_01761 | chr11:75263658-75266843 | Aorta | | SE_02589 | chr11:75264863-75266669 | Astrocytes | | SE_06644 | chr11:75263622-75267359 | Brain_Hippocampus_Middle | | SE_26322 | chr11:75264348-75266703 | Duodenum_Smooth_Muscle | | SE_27171 | chr11:75264334-75266795 | Esophagus | | SE_29498 | chr11:75264520-75266873 | Fetal_Intestine_Large | | SE_29751 | chr11:75264058-75277502 | Fetal_Muscle | | SE_33216 | chr11:75265020-75266095 | H1 | | SE_37818 | chr11:75264640-75266993 | HSMMtube | | SE_39032 | chr11:75265722-75266883 | IMR90 | | SE_40927 | chr11:75264057-75266869 | Left_Ventricle | | SE_42258 | chr11:75264138-75266814 | Lung | | SE_44656 | chr11:75264646-75266775 | NHDF-Ad | | SE_45028 | chr11:75265583-75266836 | NHLF | | SE_46693 | chr11:75264540-75265644 | Ovary | | SE_46693 | chr11:75265645-75266716 | Ovary | | SE_48900 | chr11:75264476-75266822 | Right_Atrium | | SE_49620 | chr11:75264802-75265588 | Right_Ventricle | | SE_49620 | chr11:75265589-75266762 | Right_Ventricle | | SE_51072 | chr11:75264382-75266796 | Sigmoid_Colon | | SE_53818 | chr11:75264620-75266861 | Spleen | | SE_54801 | chr11:75264002-75267260 | Stomach_Smooth_Muscle | | SE_68808 | chr11:75263713-75266870 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr11 | 75266419 | 75266727 | | chr11 | 75264594 | 75266327 | | chr11 | 75265416 | 75265853 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I075552 | chr11 | 75264019 | 75267304 |
|
Enhancer Sequence | CACCCATGAG GTTGGCCCTG ATCCTGTTTT TATTTAAAAT TGTGATATTT TGTTACTCAT 60
AGAATTTTTG CATTGATTTA GATTTTTTGA AATATTGCAT GAAACATGAT TTACTTTGAT 120
GACTGAGGTT TTCGGTGCTC TCATTAATTG TGCCCCCAAG GCAAGTGCCT CACTTGCCTC 180
ACCCTATTCC CAGTCTTCTC TGCTTGGTGT GCACTTCTCA ACCTTAGGTA GCCTCCTCCA 240
AGAAGTCTTC CCTGACCCCT GATCCCACAC TGGATTGGTA CTTCTGGGCT CCTTCTGGCT 300
GGGCTACAGT CCCAGAGCTC CTCTGCTTCC TCCCCTCCGT CCCATTCCTG AGCACCTGGT 360
GTGAGTCCCA TTGTTTAAGG GAGTAGATTT GGTTTGCTTC TGTGTTCCAG AAGAGGGCCT 420
GGCTCGGAAC AGTTGCTCAG GAAAAGTGGG TTTTGAGAGA AAATGAGTGG TCTGCCAGTG 480
CTTGGAATTT TATGTCAACA CGATGTCTTT GGGTCAAGCC CTTCTGTCTC CAGAAGTTCC 540
TTGGTAAAAC CTCTATGGGG TAATCCTTGG GCAAGACTCT ATCTCTGAAA ATGCCCAGTG 600
GTGGCAGAGC CAGCTCTGTG GGCACTAGAC CTCCTCATCC CCCGCCCCAC CACCCATGGG 660
CACCATGGCA GAGCCAGCCT CACCTTAGGT GGCAGGGCAG AAACCTGGCA TGGGTGTGGG 720
GCTGGGCCAG TCCTGTGGAC CTGTGATGCT GGCCTGTTGT TGACCCGCTT GCTCCTGCAC 780
AAACCGTGCC AAGCTCCATC TTCAGGCCAA GCCCTGTAGT TCCTCACCTC AGGGACTCAC 840
AGCCTTGCTC CAATAACCTG GGTCCCTGCC TTGTTCGGGG GACCAGACTT GGTGTCTAGA 900
TTTGTGTCCG GGACAGAACC TTTCTAGTAC TCAGCACCAC CATCGTTAGT CTTCTAGGTA 960
CCCTGTGTCA GGGAGCTGGA GGAAGATGCC TATGAATTCC TGAGCCTCAG CATATGCTCT 1020
GATCAGTCCT TTACCCCAAC TATGTCCCAG GACTCCCTCA AGCCTGGCCA GTGTTTATCC 1080
AGCTCTCCCT TCTTCATTGT TCTAACAATT TAAAGCCTCT GCCTGGGGCC TGGGCAGGGT 1140
TAACAAAGTA ATCAACTTTA GGCAGTGCCC AAAATGTGAG TGGCTCCCAG AGTCCTTGGC 1200
GACACTGACG CCAGCACAAA CCTTCTGACA CCCTTGCAGG TATGGCCCAG TGGCTGCTGT 1260
GGACAGAATC CCAGGCCCCA AGCAAGGAGA GCTAGCTTCA AACCCAGCTC TATAATCTCT 1320
GCTTGTTTGG GGCTCAGTTT CATCATCTGC AAAATGGGGA GAAAATGCCT ACCTCATAGC 1380
AGGGTGATGG GAATTAATGG AAAATGCAGG AGCTCCTGGC ACACCACAGG CACTGGGAAA 1440
TGCTAGCTCC CTTTCTCCTG TGCTTGCTTT TGGTGTGAAG ACCAGTCAGC TGTGCTCCCT 1500
GGGGACTCCC TTCCCGCTCC AGCTCCCAGC CTCTGAGTTC TTTTTCACAA CTCTCTGTGC 1560
CAACTCAAGA GATGGGGAAA CTGAGGCTCA GAGGGATCAG GGACTTGCTG AAAGTCAGGT 1620
GTAGAGTCAG AGGCTGAGCA CAGGCTGGAA TCTAGGAGCT GGGGCTCGGC CAGAGGTCTG 1680
GGCTTGGCAG GTGGCCAGCT CCTCCCCTCC CGTGTTTCCC CATCTGGCCC TGGGAATGCT 1740
GAGCCTGTGA AGCACAGCTG TATATATAGC ATCAGCTATG GGCTCCTCCC CCATCACACA 1800
CACATGGGCA CACAGACACA CACAGACCCA GCCAACAGCG CTGGGTGCTT CCATGAAAGG 1860
CGTGTTTCCC TCCTGAGTCA GAGCAGACCC CGAACAGACA GCCTTTGGGC CTGGCTGGGC 1920
TGCAGTCCCA GAGCTCTAGG CGGCCCTGAG AGCCAGCCCC CTCCCTGCTG GAACCTCTGG 1980
GCAGCAGCCA GCACAGCTGC ATCCCCTCAG CAAGGCCTGC AACGATAGGC CCACGTTGCA 2040
TCAGCTCGGC CTGTCTCTGG GCCTGCTCCG GCCCCAACAG CCAATGGGGC CCGGCCGAGT 2100
GTACAGACCC CAGCACTGGT CCAGCCCACC CCACCACCAT CACCGTGCGG CCGCCTGGTC 2160
CTCCTTCGCT CTGGGCTAGG AGGAGGGCAC CGCTGCTCCA TCGCCTGTGG CATGGCCCTC 2220
TCTCTGTGCC CCTGCCCCCA CCAGTGGCTC TGCCAGCTCA GCCTTGGTTT CCCTTCCGGG 2280
AGGTAGCAGG GTCACCCCTT GGCCTGGCGT GGGCCCATTT CTCCACAGCC TCTGTTCTCC 2340
TCAGGCTCTG TGCTTGCTCT GATCCGCATC TTTCACCTGT GGCATCTTTC AGTTACTCTC 2400
CTATAACCAT GATTCACAAA TTGTCATCTT TGGACAGGCC TTCTCTCCTG ACAGAATTAC 2460
GGACATTACA GCCTCCTGAT GTCTCCAGTC TATGGAGCCC ACCAGCTTCC CCCAGAGCTC 2520
ACTGCCTTCC CCCAGAGTCT CCATTGCAGG AAAGGGACCA TTTGCCACTT GTTCACCAGG 2580
CCAGACACCA GAGAGTCCTC CTTCCCCCTT CTCCCAGGCC CTCCGTGCCC AACCCACCGC 2640
CACTGGGCCC TCTCCAGCCC GAGGCCCCTG CCTGGTCTGG GCACCAGCAT CTCTCTCCAG 2700
GTTACCGAGC CATTCTCTCC TCTGGCCTCC CTCTCTCGCT CTCCATGCAG CAGGCAGAGA 2760
ATGCAAAAAC GCAGGGTGAC CTGTCACCAA CTTCCACAGC TTTAGTCACA CGTACCCCCC 2820
TCCCATGGTG GCCTCTGTGG GGTCTCGTGC CTACCCTCCC CTGGCTGCGT CCCATGAAAT 2880
CTTGCCAGGA TTTGGCTCTT TAGCCTGAGG CCTAAAGCCA GCAGGTCTGG GCTGGTGGGA 2940
AATGCCAGAC CTGGCCAGAG GAGCCACAGC CCCAGCCTCC CACCTTCCCC AGGGTTGCAG 3000
CGCAGTATCT CTGAGCCCCA GGCTCAGCAC CACCACTTCC CCAGCCACCC TCGGACAAGC 3060
CCCCTTCAGG CTGGAGCTTG ATACCCTTCT GGGTGTTTCT TTTCTATTCA CTTGGTTGAT 3120
TTTTTTTTTT TTTTGGCTGA 3140
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