| Tag | Content |
|---|
EnhancerAtlas ID | HS184-29492 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr8:67433120-67436100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr8:67434868-67434883 | GGGGCAAGCTGACCT | - | 6.79 | | Foxd3 | MA0041.1 | chr8:67434919-67434931 | AAACAAACATTC | - | 7.22 | | Twist2 | MA0633.1 | chr8:67434272-67434282 | AACATATGGT | - | 6.02 |
|
| | Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
| SE_01716 | chr8:67429742-67436254 | Aorta | | SE_02451 | chr8:67433314-67436204 | Astrocytes | | SE_03311 | chr8:67433479-67436032 | Brain_Angular_Gyrus | | SE_04061 | chr8:67430640-67436433 | Brain_Anterior_Caudate | | SE_04954 | chr8:67429436-67437004 | Brain_Cingulate_Gyrus | | SE_05993 | chr8:67429348-67436398 | Brain_Hippocampus_Middle | | SE_06856 | chr8:67433061-67436877 | Brain_Hippocampus_Middle_150 | | SE_07872 | chr8:67429503-67436499 | Brain_Inferior_Temporal_Lobe | | SE_08914 | chr8:67434546-67435869 | Brain_Mid_Frontal_Lobe | | SE_20725 | chr8:67434200-67435972 | CD56 | | SE_36142 | chr8:67433124-67438712 | HMEC | | SE_37326 | chr8:67433029-67437102 | HSMMtube | | SE_38764 | chr8:67433389-67436357 | HUVEC | | SE_41451 | chr8:67429480-67436697 | Left_Ventricle | | SE_43305 | chr8:67429741-67436164 | Lung | | SE_43493 | chr8:67429918-67438662 | MCF-7 | | SE_44736 | chr8:67433000-67436682 | NHDF-Ad | | SE_45011 | chr8:67433006-67436334 | NHLF | | SE_45855 | chr8:67428834-67436952 | Osteoblasts | | SE_47153 | chr8:67419159-67438708 | Panc1 | | SE_49256 | chr8:67429893-67436269 | Right_Atrium | | SE_51745 | chr8:67433246-67436747 | Skeletal_Muscle_Myoblast | | SE_54868 | chr8:67429551-67438280 | Stomach_Smooth_Muscle | | SE_56182 | chr8:67433214-67436443 | u87 | | SE_63533 | chr8:67433188-67436780 | HSMM | | SE_65207 | chr8:67433428-67436325 | NHEK | | SE_68177 | chr8:67418890-67478365 | TC32 |
|
| | 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 |
| GH08I066516 | chr8 | 67428306 | 67440606 |
|
Enhancer Sequence | TATCTTTCTC TAAATGTCCT AGGAAAGATT AAATAAAAAA ATCAATGCTG ACATGCAGCT 60
GGTATGCACC AGGACGACTG CACATGTGTG AAAATGTCCG TATGCCTCAA CACTGTCTGG 120
TACCAGCCAA TCCCAGAGCT CCCTGAAGCA TCCCCTGTCC CCTATTGGCC TGATTACCCA 180
AGCCCTCCCC AGGACTCTTC GCTGACCTCC CCAGGGATCA GCAGCTGTGG GTAATGCCTG 240
ACACTGTATT GGGGGGGTGG GCAGCAGCAG GGTGAGGGTG GTTTCAGGAC CTGCCCAGCA 300
TGGTGGCTGG CATTTATCCT CATTGGTCAT TTGTCCATGC TCTTCCTGTT AAAAATTTGG 360
ACTGTCCTCT GGAAGCAATG CATTTGGGTG CACCTGTCTT GTAAGTTGAA TTATAGACCA 420
CATAAGTAAC AGGCAGGCTA AGATAGAGAG GGATCACCCC TTAAACTGTC ATCAGTCATT 480
TATGCCTTAG AGTAAGTGAA TGAAGGAATG GAGAGGAGGT TTTCGTAGGG ACTGGCAGGT 540
AAGGGGAAAG GAAGGAGGTG TAATACCAAG GGAAGGAAGT GTTAGGAGCC CAAATGGGGA 600
AACAACTTCA GGCTATTTCT CCTCACTGCC TAGAGCCCTA CTTATCCTCC AAGCCCTACA 660
TGTTCCCCAC CAGCATTTTA AATTCCTTGG ATTCAAGGTG CAATACTCCC TGGAAGCAGA 720
TGTCCTCCAT GAAGAAGAAG GGAAATGGGC CCCACAGGTG GTGCTGCAGA GTCCCACTCG 780
CCAGCCACGG ACACCACGGA CACCCAGGAC AGTGTAGACG GGTGGGACAA TGGACCCTGG 840
ATGGTGAAGG AGCACCAGAT TCAAGGCAGA ATGCCTGGCC CCAAGACTCA GCCCCACACT 900
TACTGGAGAG AGAGAGAGAG AGAGAGAGAG AGAGAGAGAG AGAGAGAGAG AGAGAGAGAG 960
AGAGAGAGAG TGTGTGTGTG TGTGTGTGTG TGTGTGTCAT TGGTCAAGCT GCCTGAGTTT 1020
CTTTGAGTCT CTATTTCCCC TCATCTGTGA AATGTGGATT AAATTACCTG CCCAGCCAAC 1080
CTCACAGGCT GATGAAAGAT CAGAAGAGAG CTGGTGTATA AAAGGACTTT GTAAATTGTG 1140
AATTGCACTT CTAACATATG GTGTTATGCT AATCCACTCC ATTCAGAAAG AAGCAGATCT 1200
GGGCGTGGGG AGAAGTGACT CAGGCAGCTG AAGACAGGAG TGAGGGCTGA AAAGCTAGGC 1260
GGTGACTGAA AATAGAACCG TTTTCAGAGC TCCCGTGCCA GGTTCCTGGG ACCGGGCTCG 1320
CCAGCAGCTG GCAGGCAGGG GCTCCAGGCT GGCCAGGCCC CAGCTACCTG CTCCCCAGTG 1380
CTGCAGCCCG AGGTGGCCAG ACGCCCCACC TGGTCAGTGC AGTCCAGCGA CCTCTGCTCA 1440
CAAGCAAGAA GTGGAGGATG AGGACCAGTT TTTTGAATTC AAATGACTCT CTCTCCTGGA 1500
GCCGCCTGCT TGCTGCCAAA TGCAGCTTTT GGCTTCTTGC CTGCATTCCT ACCAGCAAAA 1560
TTAGCCCACA GATGAAACCT ACAAAGCACA TTGGCCCAGG AGACCAGAGG CCCTGCCTGC 1620
ATGCTCCAGC CCCACGAGGG AAGTGTCCCC TGCCCATCCT GCCTTAGCTG AGCCCCAGCC 1680
CTCCTATTTT GAGGCAGGTA ACAGGGCCGG TACCCACAGG ACTAAGCACT ACTAAGCCAT 1740
CAAGGTCCGG GGCAAGCTGA CCTGTGTGGG TGTAACTAGG CACAGACTTG ATGTTTCATA 1800
AACAAACATT CCTTCAAGGC ATTTCTGCTG CTAGCTCAGG CCAAGGAAAG CAAGGTAATA 1860
ACTCAAGGAA CAGTGACCTC ACCAGGAAAG CAGGCTCCTC AGTCTCACAC ACAAATCCCA 1920
CATCCCCATA TATCCCAGAC TCAGTGTGTC ATGAAAAATC CCCAAGAGGC ACTCCCCTGT 1980
AAAGGGAGCA GGTAGCCAGT TGAGAAGCAG GCTGGGAGCA GGGAGGGAGC TTTTTTCCAG 2040
CTGCCTAGAG ATACCACCAT CTCAGGAGCA AGGAGTGGGC AGTGCAGAGG GTCTCTGCCC 2100
TCTGTGGGTC CTGCCCTCTT GCCACCACAG AAAGAAAGCA GAACAAAGCC GAAACTATTT 2160
GTCATTTTGG CTCTTTCAGG TCCTGGCCAG GCTCTGTGAC AGCATGCTGC CTCGGCAGCC 2220
ACTGGGAGCT GGAGCTGGAG CTGGGAACTG GGAGCCAAGC ACTGGGCCCT GTTGTGAAAC 2280
CACTCAGCCT GGTCCTGTTT CATTTCCCCC ATCTGCTGCT TTGTTCTTCC TCAGGATGTG 2340
GTGAGAGGTG GAGACTGGGG AAGGAAGTAG GAAGAAGAGA GGCCTGGAAG TCCTGGCTGT 2400
TTATTCCCTG ATCCTCCACC CTGAGAAGAG AGAGGGCAGA AAGCCACCCT GTCTCTGAAC 2460
CTGGGTAAAT GCACCCCCCA GGTACCCACC TGTGTGCTGG AGGCTACTTG AAGCTACAGG 2520
CTAAACCCAC ACATCTTCCT GGGCCCTCCA GTTGGGCCGC AGTGGACTTT AACACATTAA 2580
GACAAATACA ACTGTATTAA CAGAAGCTAA CATTTATGCT TTACATGTGC TGGACACTGT 2640
GCTAAGTGCA TCAAGTACCT CAGCTCATGC AATCCTCCAA ACAACACCAT GGGATGGCTC 2700
TTTCATTTAC CCTATTGGTT TACAGAGGCT TAGAGAGTTC ATGAGGTTGC TTGAGGTCAC 2760
ATAGCTATGG GTGGCGGCCC AGAGATGGAC TCAGGCAGTT GGACTGCAGA GCCCACTGCA 2820
GGTAGATGTC CAATTTGTAC ACTGCCCGAA GGTGCCCTAC TAGCGACAAG TACTGTGTGC 2880
ATGGGCACTG CCTCCACTCA AAGACAGCAC TGTCCACTTG CTTCGAGGGG TCAGCTTCCT 2940
AAAGTGGCAA AATTCACTTG AATATTTCAG TTAAAAGTTG 2980
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