| Tag | Content |
|---|
EnhancerAtlas ID | HS112-10097 |
Organism | Homo sapiens |
Tissue/cell | KELLY |
Coordinate | chr3:127492850-127495580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr3:127494482-127494495 | AGATAATTAATTC | - | 6.09 | | ZNF263 | MA0528.1 | chr3:127493929-127493950 | GAAGAAGGAAGAGGAGGAGGC | + | 7.16 |
|
| | Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
| SE_00025 | chr3:127483267-127497327 | Adipose_Nuclei | | SE_03564 | chr3:127494744-127495299 | Brain_Angular_Gyrus | | SE_05617 | chr3:127494122-127495932 | Brain_Cingulate_Gyrus | | SE_07382 | chr3:127494070-127495743 | Brain_Hippocampus_Middle_150 | | SE_07763 | chr3:127494148-127496042 | Brain_Inferior_Temporal_Lobe | | SE_13552 | chr3:127491471-127496788 | CD34_Primary_RO01536 | | SE_23130 | chr3:127492064-127493209 | Colon_Crypt_1 | | SE_29692 | chr3:127493933-127495810 | Fetal_Muscle | | SE_31809 | chr3:127494195-127495203 | Gastric | | SE_32550 | chr3:127493077-127495870 | GM12878 | | SE_33427 | chr3:127492812-127495811 | H2171 | | SE_37481 | chr3:127493071-127496079 | HSMMtube | | SE_39295 | chr3:127493681-127495672 | IMR90 | | SE_40646 | chr3:127494193-127495768 | Left_Ventricle | | SE_42255 | chr3:127490649-127493743 | Lung | | SE_42255 | chr3:127494237-127496113 | Lung | | SE_44967 | chr3:127493515-127495610 | NHLF | | SE_48433 | chr3:127494041-127496094 | Psoas_Muscle | | SE_48608 | chr3:127494244-127495777 | Right_Atrium | | SE_50388 | chr3:127494224-127495899 | Sigmoid_Colon | | SE_51198 | chr3:127493447-127496383 | Skeletal_Muscle | | SE_52979 | chr3:127494228-127495891 | Small_Intestine | | SE_53526 | chr3:127493721-127495452 | Spleen | | SE_54601 | chr3:127492851-127495764 | Stomach_Smooth_Muscle | | SE_55690 | chr3:127492696-127496509 | u87 | | SE_58865 | chr3:127447411-127515741 | Ly3 | | SE_67490 | chr3:127492696-127496509 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 127494660 | 127494939 | | chr3 | 127493664 | 127495200 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I127766 | chr3 | 127485842 | 127497932 |
|
Enhancer Sequence | GTTCAGAAAT CACACACATC ACAGTATACT GCTCCCCTGC TCACAGCCCT CCCTCCAGTG 60
GCTTCCAACA TCCCAGAGCA GCCTCTGTTC CTCCTCCTTG GGCCCACAAG GCCCCTGCCC 120
ATCACTGCTC ACCTGCTGTT CTGTCTAAGC TCTGACCATC CTGGCTTGCT GGCGACCTGA 180
GAGCACCCTG CTAGCCCCTG CCCCCGGGCC TTTGCACTGA CTGTTCCCAG CTCTAGACTC 240
CCTCTGCCAC CCAGACCTTT GCAAGAATGG GTCCAAATGA CTGCCACAGC CTCTTGAAAG 300
GCTTCCCAAA CTGTTGGGCA GAGGGAGCCC CTCTCCCTGG CAGCCTCCTG CCTCTTGCCT 360
CCCCTGCACT TGGCAGGACA TAACACCTCT CCTTATTCAC TCATGTCTGC CTGGCTCACT 420
GCTGGACCTC TGTGCCTAGA ACAGTTAGGA GTGCAGTTGG GCATTCAGTG AATATCAAAG 480
AATGAAGGAA GAAGAGTTCC TTCACCTGAA TGCTCTTTCT CCATATTTCC CTGTTCAATT 540
TCATCTCCTT GAGGAAGCAT CCTTTGAAGT CTGGGACAGA ACTTTCAATA GCTGCAAAGT 600
CTCCCTGCAC CTTTCTTTGC AGGTGAGCTG GCAGGTACTT CGTGTCTAAT AGATGCCTGG 660
CGTTGTGTAT GGTTTGTTAC ACACACTCTC TCAGGGGTCC TCAGCAGCAG CAGCAGCAGC 720
AGCAGCACCC CCAGGGGCTG TTAGAAATGC ACATTCTTGG GCCCCACAGC AGACCAACTG 780
AATCTGAATC CTGGGGTGGG CCCAGCCATC TGGCTTTCAA CAGGGGATGC TGCTGCCACT 840
GGAGTTTCAG ACCCTGCGCT ATCTCATTTC ATCTCCACGG CCACAGAGCA ACCTTGTTAT 900
TATCATGGTC CTCATTTTAC AAACGAGCAA CTGAGCCACA TGGAGGTTTT TGTTTTGTTC 960
AACAGAGGCA AATGACCTCA TATCAGAGAG GGCACACAAA CTCATATCCG AGACTTACAT 1020
CAAATAAACT CAACAGGCTT TCATCAAAGG TAGAGCATTC ACTATGCTTA ATAGTGAATG 1080
AAGAAGGAAG AGGAGGAGGC AAGGGGACGA AGGGAATGAG TTGGGGAATA GCAGAGACTA 1140
TGGGGGTCTC AGGGTGGCAC AGTCCACTCT CCCACACTCT ACAAGTTGCA GCAAGTTCAC 1200
TGTCACCCAC CCTCGGAGTT GGGCCCCCAA GGAACTCTTG AAGACTTAAA GGGCAACTCA 1260
CTCCATTATT TTAATTCTCA TATTTACTAA GGCAAGAAAA ACGGTTAACA CATTTTTCAA 1320
ACGTTTCAAA CAAAAATATA TTACTTACAA GAAATAAAAT AAACCTATGG CAGTTTATTT 1380
TAGAATACTT CCAGCAAGCG ACCTTGACTC AAATCTGTCT CCCTGGATGA AAAACACCCA 1440
TATACAATTA TTCCCCCTGA ATTTCCTAAA TACTCTTCTT CTGACTGGAT AGGACCCACC 1500
CGCCAAGGAG AACCACGCGT AACTGCCGCC CACAGACATT CCCTCAAAAC TTCCTCTTCT 1560
CACATGCCCC AGCTGAGTTA AAAAAAAACA CACACACAAA GCCCTCTTTA ACACTTTCCC 1620
TCAAATATTT GCAGATAATT AATTCACTGT TCATCAGTTG AGGATGGTTC GTTTATACTT 1680
TGTAAATACA GAGGAGGCTT CTCTGGCCCC AGCAAGTGCT CCTGGAGCCG AGAGTGCGTG 1740
TTAGGAAGTC AGGAGGCTGC TCCCTGGGGA AGGGCCCTTT CCAGCAGGAC TGCAGGGAGC 1800
AGGCCTGCGG GCAAATGGGC CTCAGATTCC CACCGTCTCT CGCAGCAGCG CCTCCTGGGT 1860
GGGTCCATGT GTGCCCTCCT CCCGGAGTCC TCCTTGCCCC CTCTGGGTGA GACTGGCCCT 1920
TCTGCCTGCA TGGAAGGCCA AGGGGTTTCC AGTGAGTCAC TGCAGCAGCT GGCAGACCAG 1980
GGACCAAGAG AACGCCAGCC CCGGTTTTCT CCCTGCTATA TTTAGAATGT TGCGGAAAAT 2040
CCCATCTTCT GGTGTCCCCA CCTGTTCACA CATGGCAGCA GCCCCTCCGT TTCTGGCTGC 2100
CCGTGCACCT CTCCCTCATG GGCTCTACTC TGAGGCCCCT CTCCTGAGGA TCTCCAAAGT 2160
CTCCTGGTGG CCTTCCATCC TTCCAGGCCC CAGAGCCTTT CCTAATAAAT CCTGTCTTCA 2220
CCAGCTCCAA ACTTTGTGCC TGTGTGGCCT CCTCTGCTCA GTGGTAGTTC TCAACCTGGG 2280
CTGCATATAA GAATCACCTC GTGTATCTTT TAAAATCCTG ATGCCCAGGT GACACCAAAG 2340
ACCAATAAAT CAGGATCTCT GAGGGGTGGG GGAGGGGGAG CCCAGGCTTC AGGATTTTTT 2400
GACTCCCCAG TAATCCTGAC AGTAGGCAAG GTGAGAACCA TGGCTCTCAA CGATCGGAGC 2460
CCTTCCTCCT GCTGACAAGC TCCCACTCTC CGACAAGACC CGGCCATCCT GCCAGCCACC 2520
CTTCTGGCCC TCCAGGCATT GAGGATGCCC TGAGCCTGGA GGTGCCACAC CCCTTCCTGA 2580
GCTGCGGGCC TTGTGGCGCC TCTGTCCCAG CAGCGCATCC ATGGCACTTA CGGGCTCTCC 2640
ACCTGCTTGG TCACCAGACT CAGGTCCAGT GGCCACACTG CTGGACCCTC TGCTCATTGA 2700
GGGGACCCGG CAGTGCCCTG CTTACGTGGA 2730
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