| Tag | Content |
|---|
EnhancerAtlas ID | HS105-66627 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr5:156942470-156945140 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr5:156943107-156943120 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr5:156943104-156943117 | GATTAATTAATTA | - | 7.34 | | MSC | MA0665.1 | chr5:156943970-156943980 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr5:156943970-156943980 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr5:156943970-156943980 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr5:156943970-156943980 | AACAGCTGTT | - | 6.02 | | POU6F1 | MA0628.1 | chr5:156943105-156943115 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr5:156943109-156943119 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr5:156943105-156943115 | ATTAATTAAT | - | 6.02 | | POU6F1 | MA0628.1 | chr5:156943109-156943119 | ATTAATTAAT | - | 6.02 |
|
| | Number of super-enhancer constituents: 17 | ID | Coordinate | Tissue/cell |
| SE_10243 | chr5:156942912-156944407 | CD19_Primary | | SE_10863 | chr5:156909781-156978888 | CD20 | | SE_14730 | chr5:156942857-156944779 | CD4_Memory_Primary_7pool | | SE_25805 | chr5:156942317-156945425 | Duodenum_Smooth_Muscle | | SE_27121 | chr5:156942543-156944778 | Esophagus | | SE_30832 | chr5:156943004-156944357 | Fetal_Muscle | | SE_36955 | chr5:156931578-156947133 | HSMMtube | | SE_40934 | chr5:156942403-156945364 | Left_Ventricle | | SE_42416 | chr5:156942579-156945185 | Lung | | SE_46096 | chr5:156942484-156945222 | Osteoblasts | | SE_48834 | chr5:156942561-156944752 | Right_Atrium | | SE_50178 | chr5:156942538-156945172 | Sigmoid_Colon | | SE_51718 | chr5:156942296-156945287 | Skeletal_Muscle_Myoblast | | SE_52470 | chr5:156942669-156945189 | Small_Intestine | | SE_53856 | chr5:156942391-156945002 | Spleen | | SE_54595 | chr5:156941720-156945392 | Stomach_Smooth_Muscle | | SE_63503 | chr5:156941760-156945350 | 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 |
| GH05I157514 | chr5 | 156941546 | 156945274 |
|
Enhancer Sequence | CTTTGCGGCC CCATAGTCTC TGCTACAACT CTTCAACTGT GCAGTGGTGG CTCAGAATAA 60
TACAGACACC TGTATATATA ATACAGAAGC CTGGATAATA CAGAAACCAA TGGGCCTGGC 120
TGTGTTCCAG TAAAATTTTG TTTGCAAAAA CACAGGATAG GCTGGATGTG ACCATGGGGT 180
ATAGTTTGCA GACCCCTGAT GTAAAGAAAG GACTGTCTCA AACTTACATT TTCTAGGGTG 240
ACACAGTGAG TACCACATGC AGCACCATCC TTTCCCAGCC ACTCTGCACT GTGCCAGCAT 300
CATGGAAGTC CTTTACAGGC CTGTGTTTAC AGTTATCCTG TCTACTCCTA CAACAGCCCA 360
CCTTACTCTT TATCCCCACC TGGATTCCGT TCCACCTGGG GAATGAATAA ACTGAGAACC 420
ACCCTAGAAG CTCCCACCTA GGCCCAGGGA GCGAGGAGCT GCCTGCTCAT TTTTACTGCT 480
GACAACTCTC TCTCTAGGCA GCAGCAGGGT CTTGCTCTCC CTATCTGTGT CTCCACTTTC 540
TGCTCTGCAT TCAGAGCCCC AAGGCTCTGT CTCTGCAGCA GGTTATAAAT CATGGTAAAG 600
CAGCCCTCCC CTTTCCTGCC TTCCCATCCT CTCAGATTAA TTAATTAATT GTCAAGAATA 660
TATTTCTGTC TGCAGAGGAT GGAGACAGGT GGAGAGGGGA TGATTCGTGA GCCTGTGAAC 720
CCAGCCTGGC CTGTTACACA CCCCCACCCC AGTCCCTCAA ATGAATCATT CAAAGCCTTC 780
AGCGGAGGGG TGTCCAGGAC TGAGAAATGA GCACGTTCCC TTATCCACCA CAGCTGCATG 840
AATCACAGCC CTGTTGGGAA CCCAGGGCTG TTGCTGAGAC ACTCTCCTTT GTAAGAGAAA 900
GATGGCTCTA GCTGACACCA GAGTCCTGGA GGCACCTTGA GTGGACACTT TTTCTCTGGA 960
GGTGTGCTGT GACTCTGGAG GTCAGGAGAT AGAAGATGCC TAATCCCTGC CTCCCACCAT 1020
GCTTCCCACT TCTCCAGCTG CTGGAGATTC ACACCCAGTG GGTTTGAAAG CCTGCACAGA 1080
GATTCCTCTG AGAACAATGC AAGGCCAAAG GGGAGAAACA CCCCACCTTT AAACAGAGCA 1140
GCTGGGCTCT ATATGCTTAA CTACTGGGGT TCCCAGGAAC TTCCATGTAA CCAAAGGATT 1200
CTGTAGCTGA AAAAAATGAC TCAAGACCAT TGTATCAGAT GATCACAGAT GCAGAACTTA 1260
AGTGGAAAAA TGTCCCAGAG TCAGAGGAGC TCAGTTTTCT TCCACCAGTC CTCCCACTAC 1320
GGGCAGTCAG GCAGGGCAGG CCAGAGTCAG TTATCTCCTC CCACGACTAT GGAGCCTCAG 1380
CTGGCTTTTA AACCAGCTTT GGATTTTGCT CCCCACACTA TTCCCCCATC CTATAGACAC 1440
ACTAGTCTTT GGAGAGGAAA CAGAAAACAT AGAACACACA CACACACACA CACACACACA 1500
AACAGCTGTT GGAAAAACCA ATATCAACAT CAGTTAAAAT AAATCTAAAC GCTTTTCAAA 1560
GCAGAGCACA ATGTTCCCTC GGCCCGGAAT GCCCTTCACC TCCACTCCTC TGCCCAGTTA 1620
ACTCCTCCTT GTCTTTTAAG ACAGCTTCAA GGGCCACCTC CTTCTGCTGC TAACATCCAG 1680
TGACTAACAC TCAAAGACCT TCTGGCCTGC AGCCTAGTGC TCTCCCCACC ACCAGGCCCT 1740
GCTGCCAGGA CACATGCTTT GGAAATGTGA CTAGGTACAG CTGCCTTAGA ATGAGCTCTT 1800
TGGGAAGATG GTAGCTAAAC TATGTGGATG GGATACAGAC AGACTGGAGT TGTGATGGGC 1860
TCTATCCTCA GGAGAGACCA AGGCCAGTGT CTGCCCTGCT CGAACACAGC GAGCGCTCAG 1920
CTCATAATGA CATCCAATGC ACAGAAGATG CACTTAGTAC TTATATGATG GAGTCACTAA 1980
ACAAAGTGAG AATTGGAGGT AACAGCTGGC TAATTTAGGC AAATATGGGC TCTGGGGCCT 2040
AAACTCACTC TTTAGGTGTC TGCTTCAATG TCAGGGAAGC TTTCCCTAAT TCCCAAAACC 2100
ATGTTGAATC CCCCATTATC TGCACTTTCA TCCCTCCTAA TGGTCCATCT TAGTGCTTAT 2160
CACACTTTGG ACCTACAGGT TTGTGTGCTG TTACTGCAAA CTCTGCGATG CCTGGGGAGG 2220
GTCTGTCTTC TTGAGATCTA TATATCCAGG TGCTTGGCAC ATAATAGAAA ATCAAGAGAT 2280
CACTGATGAA TAAATGAAAT ACATGATGAG CCAGGTGAGG GTTCCTCAAA TTCTTAGAAC 2340
CTGTCTGATT TGAGGAACAT GGAGTTAAAG GCTGAACTGC TATGCCTTTA GGTCAGTGGT 2400
TCTCAAACTT GACTGTGCAA CCCAATCGCC CAGAGGTCTT GTTAAAACAT GGATTTCTGG 2460
ACCCCACCCT GACAGTCTGG GATTCAGGAG GTCGGGGGCA GGGCCCGAGA ATTTGCATCT 2520
TACACAAGGG TGCTGCTGAT GCTGGTGCTC TGGGGACCAC ATTTTGGGGA CCATGGCTTT 2580
AGGTCATCAT TTGGCATCAA CATGATTATA AAAATGGACC CACACATGGG CAAGAATACA 2640
GTTTTCAGTC GGATGACTGG GAATATATTT 2670
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