| Tag | Content |
|---|
EnhancerAtlas ID | HS094-36926 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr6:143166040-143169310 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ALX3 | MA0634.1 | chr6:143167670-143167680 | TTTAATTAGA | - | 6.02 | | Arid5a | MA0602.1 | chr6:143168957-143168971 | CTAATATTAAAAAA | + | 6.21 | | Gfi1b | MA0483.1 | chr6:143167387-143167398 | GGCTGTGATTT | - | 6.02 |
|
| | Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
| SE_02780 | chr6:143165105-143169364 | Astrocytes | | SE_10699 | chr6:143162811-143168578 | CD19_Primary | | SE_11156 | chr6:143162278-143180970 | CD20 | | SE_11815 | chr6:143162557-143168524 | CD3 | | SE_14877 | chr6:143162636-143168810 | CD4_Memory_Primary_7pool | | SE_15576 | chr6:143162719-143168116 | CD4_Memory_Primary_8pool | | SE_16108 | chr6:143162680-143167736 | CD4_Naive_Primary_7pool | | SE_16718 | chr6:143162822-143168097 | CD4_Naive_Primary_8pool | | SE_17071 | chr6:143162245-143168547 | CD4p_CD225int_CD127p_Tmem | | SE_17297 | chr6:143162160-143183420 | CD4p_CD25-_CD45RAp_Naive | | SE_17761 | chr6:143162286-143180780 | CD4p_CD25-_CD45ROp_Memory | | SE_18234 | chr6:143161974-143180893 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19102 | chr6:143162606-143169273 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_21816 | chr6:143162912-143168400 | CD8_Naive_7pool | | SE_22290 | chr6:143162230-143168539 | CD8_primiary | | SE_30305 | chr6:143165934-143169684 | Fetal_Muscle | | SE_32593 | chr6:143162628-143179878 | GM12878 | | SE_37346 | chr6:143165833-143169607 | HSMMtube | | SE_46005 | chr6:143162490-143170418 | Osteoblasts | | SE_51498 | chr6:143165391-143170022 | Skeletal_Muscle | | SE_52106 | chr6:143166282-143169409 | Skeletal_Muscle_Myoblast | | SE_58650 | chr6:143140122-143209359 | Ly1 | | SE_62207 | chr6:143093923-143269986 | Tonsil | | SE_63932 | chr6:143166268-143169582 | HSMM |
|
| | 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 |
| GH06I142841 | chr6 | 143162342 | 143180325 |
|
Enhancer Sequence | AATGCAAACA GGCACACCCT AGTGAGACCA CGAAGTGTGT CTTCTACAAA TCTCTTCCCC 60
TTTCTATCCT GGTCCTGTTC AGGTGACCTG GCCTAACCTG GACATGGGGT CTTTGCAGGC 120
TGCACGCTGC ATCTACTGCA GAAAAGAGCT GGTAAGATTT TTCATGCTAG GTTGTCAAAA 180
ATGTAACGTG TTCTCATTAT GAAAACATTT ACATTAAGAA AACAGCAAAA ACAAACAAAA 240
ATCTTGGGAC ATCATGAAAC TTAATACAAA CAAATAACTG TTGGTGAAGA GACAGATTTG 300
GGGGAGGGGT TTTGCAAGAA TAGAAGCAAG ACTTCCTCCT CTGTGGGAAA TATTAGTAAT 360
CCTATTAAGG CACAGTGCAA GGTGTGTCAT AGACACTAGA AGCAGATATG GTTTACTTTC 420
AGTTCTCTGA GGTGATTCTT ATTGGAATTG AAGTGGCTCT TCTGAAAACA ATTAATCAAC 480
AATAAGTTCT CTCTCCCTCC CTCTCTCTCT TTCTCTCTTC AAAGTGTGTG TGTGTATATA 540
TACGTATGTC TTTTGACTAA TTATTAGGCG TAGTCCCATT TTTTTCTCCT TGGTACCTAT 600
CACTATAATC ATCTGTGTTT CTGTGTCACC TGCTTTTAGA ATTACACATG GATATTACCA 660
GAAGTTACAG AGTTAAATTT GCAACAGCAC AGACTTCTAA CTACAAGCCT GGGACCATGG 720
TGGAAACAAA GGTTCAGTTA AGGAAGATTT CCCGAGCCAG AATTGATGTC CTCACTAACC 780
AGGCTGCCAG GCTTAAATCA AATGAAGGTC GATGCAATGT CCCCAGAGGA AGCTGTTCAA 840
CTCGCCGGGT CGGTTCCCCA GAGCCCTGCC AAGGAGGCTC CTCAGATTGA CAGCGCCCTG 900
GCAGAGCTGC TGTCTTCCCC AGGCAGAGAG GCCCTCCCCC GGACAACAAG CTGGGTGCAA 960
ACTCGTCTTC CGCAGACACC AAAAGAGAGC ACAGCAAAGC TAAGCGACTG GGGACAGCCA 1020
CTTGTGGCTG AGACAAAGGC AGGCTCCCCC TGCCGCAGGA CGATCACTAG GACTGTCAGG 1080
CTGTCGAAAT GTATATTGCA GACAGGACAT CCCTCCTGGC ATCCAGTGTG AGCGAAGTCC 1140
AGGCCACGGC AACAACAGCC TGGCCTGAGG ACAGCCTGCA CCACACATCA AAGCCAGAGG 1200
CCCTGGGAGG CTGGCCAGCC GCCAAAGACG CCTGAGAGCG GCAGGGGAGT GTGTTGCCTT 1260
AGGACAATAG CAAACTGGGA CGTGGTAGAG TCTGTAAATT CCAAGCACTG GGGAGGTCTT 1320
CTCAGAGATT TTACCCTCTC CTGTCAGGGC TGTGATTTAA TTTCCTTTGA AGAAAAAAAA 1380
AAAGAAAAAA GAAAAGAATA TACATTCCCA AATCTTCTGT CTGCAAAGGC AGACACCACA 1440
ACGCAAGCTT AATGCACTCT GGTCCTTCCC GGCCAGCGGC CACTGTCTAA CACAATACAG 1500
CTAAGTGAGA TGTGACATTC TCCCGGTCCC CTTAATAGGG CATTAAGTCT AAGGAGTACT 1560
TAAGATCATT TAAATGCAAA CATCATTGTT CCATTGCTAC TAGACTCCCA GATATTTCCC 1620
ATCAATTCTG TTTAATTAGA GTAGCACCAC ACGTTAATTA TAACCTGACA GTTTTATTGA 1680
TTTCACAGGG CACATCATAC AGTCCCATTT TAGGTACCAA GGACTTAAGG TGAAGCATGA 1740
ACCTCTCAGT CACAAAGATG ACTCAGCCTC TTGGGCTGAT GAGGTTCTGA TTCTTCTACC 1800
AGGAGAGGTT TACCCACTTG CTCAACAGAA ATAGTTCAGT AATCATCTTA TGTCCTCACT 1860
TATTTCACAG CGTTTTGCAA AACAACACAT CAAAAACAAA CTAAGGAAAA AAAAACCTGT 1920
AAGAGTGTAA AAGAAATATC CATCTCCCTC TGTTCTGTGG TCTTAATCTG CAATTCTTAA 1980
GGACCAGGAT GAGGTGCTGT GAAGGCTACG CAGGTAAAGC TGGCACCAAA CAGAAATATG 2040
GTGCACTTCT GCCCCTGAAG CGACTGGCCC CACTTTGAGA AGCCATGCTG TAAACATGCT 2100
CATTAGAACA GAGAGGACTG GTCAGTTTTC CTTTCAGAGG AAATGAATAT GAGTTGAGAT 2160
CACTCAACTC TAATCCACCC TGTACCTCAG GGTTATACTC CCAGCAGCAC ATGCTCCACT 2220
AAGCCAGCAG TTTGTCATAG CCCAGCGTGT CATCCATAAT GGCATGTTGG GGGTGGAATC 2280
ACTTCCAATT CCTCACTAAT CTGGTGCGGG GAATGCCAAG GTACAGAGTT TTACTTGATT 2340
GCATAAAACA TAGAGCTATT TTCAGCTTCC AAATCATCGT TCTGGCTCTT TCACCAGTCC 2400
TAAAGCCATA TTACAACCCT TTAAAAACAT CTTTTCTATT CGGTTTTCCC TTATTTTAAT 2460
ATAAGCAAAC ACTTAAAGTA ATCCCACTAA GTCTCTGAAA TATGAAGCCA TGAAATGTTA 2520
GAAAAAAAAA AGACGAAAAA GAGTTTAAGA GTTTTACACA TATTTGCGAT TTAAAATGGT 2580
CACTGCTGCT ATGGTAGTGG GACTTGAGTT ATCTCCAAAC TCCTTATAAA AACCCTGGGC 2640
AATTAACACT TAGCAGGACT TCGGTGCCTG ATGACAAAAT CAATTCTGTT ATAGTCACAC 2700
TTCGAAAAAT GACTTTGAAG AGTAACAATA AATAATGAAA ATTAAACAAC TGCTAACTGA 2760
TATAGGAAGA ACTTCAGCTA TTTCTGTAAT AATTCCACTG GGATTTGTGC TGAACATTAT 2820
AAAAACAGGA TGTTTTGTTT GTTGTTCTTC ATAAAAGACT ACTGAACCAG TATAAGACTC 2880
CAAAATATAT GAAGACTACA AATCTACATG AAGTCTACTA ATATTAAAAA AAAGCTAAGT 2940
GGAATTTTTA TTCATGTATT TAACATTTTT GCTCAATGTA AGATGACCTC AGGAAACATG 3000
TTTCTTATTT TTATGAAAGC CAAAAGGAAA CACAGTTATA TAACATAATT CTGCAATGGT 3060
TCAGCATCAC AGTGCAGAGA ACTTAATCCT AAATATAGGA CTGTCACAAA TCAGTCTTCA 3120
CTGCTAAGAC TTCTTATATT TAACATTAAC AACGGATTAT CCCATGGTAA CCAGATACCT 3180
GTTCCATTTA GTTAGAGGCT AATCCTAACA ACATAAGGAT TCCAATAGCA AACTTTTTTC 3240
TAATGTTACC ATCAATGAAC TGTGATGAAG 3270
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