| Tag | Content |
|---|
EnhancerAtlas ID | HS138-03893 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:235060560-235063390 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arid5a | MA0602.1 | chr1:235060566-235060580 | CTAATATTAAAATA | + | 6.1 | | MAFG | MA0659.1 | chr1:235061810-235061831 | TTAGTGCTTACTCAGCTCTTA | + | 6.17 | | MAFG | MA0659.1 | chr1:235061810-235061831 | TTAGTGCTTACTCAGCTCTTA | - | 6.27 | | MAFK | MA0496.2 | chr1:235061811-235061830 | TAGTGCTTACTCAGCTCTT | - | 6.13 | | NFAT5 | MA0606.1 | chr1:235062674-235062684 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr1:235062674-235062684 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr1:235062674-235062684 | ATTTTCCATT | + | 6.02 |
|
| | Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
| SE_01974 | chr1:235059961-235063410 | Aorta | | SE_09160 | chr1:235061465-235063648 | CD14 | | SE_28260 | chr1:235061300-235063291 | Fetal_Intestine | | SE_32179 | chr1:235060278-235061264 | Gastric | | SE_32179 | chr1:235061895-235063205 | Gastric | | SE_32492 | chr1:235060770-235064190 | GM12878 | | SE_38692 | chr1:235059788-235063226 | HUVEC | | SE_40653 | chr1:235060247-235063362 | Left_Ventricle | | SE_42317 | chr1:235059687-235063343 | Lung | | SE_45558 | chr1:235059937-235062978 | Osteoblasts | | SE_47119 | chr1:235057035-235066598 | Panc1 | | SE_48655 | chr1:235060505-235063308 | Right_Atrium | | SE_51333 | chr1:235060424-235063169 | Skeletal_Muscle | | SE_53330 | chr1:235060084-235063556 | Spleen | | SE_56739 | chr1:235060367-235061108 | VACO_400 | | SE_56739 | chr1:235061119-235061424 | VACO_400 | | SE_56739 | chr1:235061921-235063595 | VACO_400 | | SE_60969 | chr1:235059965-235155853 | HBL1 | | SE_61435 | chr1:234961094-235124239 | Toledo | | SE_62329 | chr1:235047040-235185428 | Tonsil |
|
| | 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 |
| GH01I234924 | chr1 | 235060099 | 235064175 |
|
Enhancer Sequence | CTTTATCTAA TATTAAAATA AGTGTGCATT TTCCTCCAAG CAAATGTGTG CCACCAGAAG 60
AGGCAGCACA ATATCCGGCA GCTGTTGGTG ACCTCTCTAC AGACATGACG GACTCATTTC 120
CGGGACCGGC CCCTTATACA GAGACTTCCA TCCAGCATCC TCACAGTGTC TGGCCTGGGC 180
TGTACAAATC CAGAGACCTA GAAACAGAAA CTGTGATTCC TCTCGAGAAG TGAGGCTGCT 240
ATGTGGCTGG CGTGCACACC ACACTGCCAG CTTCGGGCTC TATTGCCTTA TCTTAAATTA 300
CAAACTCTAC CAGAAGAAAA TGTCACCCTT CTGCTGGGGT CCGGAAGGCT TTGTGTGTGT 360
TAACAATCAT CTTGGAACCT GCGCTCAAGA CGACCTCAAG CACACTTTGT TCTTCAGCTC 420
TGGACGTGTC GTGGCCGTCA GGGTGAAGAG AGAGATGAGA ACAGAGGCTT GGACAGGACA 480
GCCCTGGCTG ACCAGTCAAG TGTAGAAGAC ACATACATAC ATTTCCTTTT TTCCTTTTCT 540
TTTTCAACTT TTATTTTAGA GTCAGGGAGT ACCTGTGCAG GTTTGTTACA AGGTATATAG 600
CATGATTCTG AGCTTTGGGG TACGATTGGC ACCCAGGTAA TGGGCATAGC ACCCAACAGG 660
TAGTTTTTCA GCCCTTGCCC CTCCTCCCCT GTCCCTGGTC TAGTAGTCCC CGGTGACTAT 720
TGTTCCCATC TTTATTCATG ATAGCAAAAA CACAGAATCA ACCCAGTTTC CCATCAATGG 780
TGAATTGGAT AAAGATGTGG TTCATATACA CCGTGGAATA CTACACAGCC ATAAAAAAGA 840
ATGAAATCAG GTCTTTTGCA GCAACATGGA TGTGGCTGGA GGCCATTAAC CTAAGCGAAT 900
TAATGCAGGA ACAGAAAACC AAATATATCA TGTTCTCACT TATCAGTGGG AGCTAAACAC 960
ATACCTTTCG GAAGGCACCA GAACACTGGT TTGTTCCTGC TTTGTCTTGG CACCAACCCA 1020
CTTGGCCCCT GACTCATCTT TCTCTACAAC ACTCCTGTTT GCTTTTCTCT ACCATGGAGA 1080
AGGTATGTCT CAGTGGAAGA ACTATGGGAG GTATTCAGCC CAAACATCCT CTAAGACAGT 1140
AAAGTGTTAA CAGCTTAGAA AGAGCTGCAG ACTATTAAAA TGTGAGCTGC GTTAGTCAGC 1200
TGAACCGAGA ATTCTCATCC TGGCCCTTGC TCTTGGAGGG AATGCATGCC TTAGTGCTTA 1260
CTCAGCTCTT AAACAGGGTT TGTTGTTTTG TGTGTTTTTG TTTCCCGTGA CTGTGTGTGT 1320
TTGACTTTTT TTAAACTGTG GTTTAAGAAA AAAAAAAAAA GTTGATCAGT AAGTCAAAGT 1380
GTCAGAACTG TCTGGGTTGA AGCAGGCACT CATAGGGAAG CAGGAAGACC AGTCTGTAGG 1440
TTTAGGGGAG GGGAGCAGAG GAAACAGAAT TTTCATTCCA CACCAAGCCT GCAAAATCAT 1500
ACAGACAGGA GAGCCCAGAC AAAGCTAAAT GTCATTTTCT TTATCCTAAT TTATTGATTT 1560
CTGCTGGCTG TCGGGAGCTC TCGGGGAGGA AGCATGCTGA GTCCATAGCT AATGCTTTTC 1620
GTTGTTCTCA CAGTTAGTGG GCCCTGGAGC TTGGGGAAGG GGGTGGCATA AGTGCAGGGA 1680
AATGGTGACG AGATGCAAAA GAATCATGGT GGCCAGAGCA GAAAATGTGT GCTCACATTT 1740
CTCTCTCTGC AGTGTTTCTG AAATGGCCTC TTCATTTACT TGAAAGAGAC CTCATGCCAA 1800
AAAATGCATA GCATCATCCC CCACCTGCTC AGTCATGCCT TGAATCTCAA GCCCAGAAAC 1860
GCAACTGCTG CCGGTGGGGG GTGCACCCCA AAAGTCCTCA TCCTGAGAAC ACCTGTTAAA 1920
AAGTCCACGA TGGCAGAAAT CCCTGGTGCT GCATGGAGAA TCTCCACTCA GGTGCGTCAC 1980
CCCCTAGACG TTAGGAAGGT CCGGGGCAGG TGTCCGGTGG GGTCAGGGAG ACACGCAGGT 2040
TCAAGGTTGT TCTACAACCC TGAGAGAAAT GTCTGGGCCT CAGAACGTCA AGAGAGCTGG 2100
TTCTTCAGAG TTCTATTTTC CATTCCGCTA CTTTGAGAGG GATGTGGGCT TTCATTGTGC 2160
TCGTTATTTT CATGAAAACT CATTACAAAA CTGAAACCAA CATCACAGAA CAATGAGGAA 2220
TCACCAGCCC ATTGAACAAG TGCAGAGCGG CACATATGAC CACTGCAATG CTTCCTTTCC 2280
AAAGCTCTTT TGCTCTTGCG TGGAGTGGCC CCCGCCACGG GCTTTCCCAG GTCACACCTG 2340
CTCCACACTT CTCTCCAGGT GCCTCTGTCC CCTGAGGCCT CACCTCGGGC CCGGGTCGCC 2400
CTGCACAAAC AGCCCCTGGG CGGGCACACA GCACTGACTC TGCTGCAGTC TCCAGGTTCC 2460
CGAAGCCAGC TGCCTACTGG ACACTGCACC CTTAAAGTCC CACCGATGCA TCCCCAACAG 2520
GGTCTCCTCC ACGGCCCCCC TTCCTGGTGA AGTCTGATCA GCTTCCAGCC ACACAGATGT 2580
GAAGACTCAT TGTCTCCAAG GAGCCCCAGA GTCCGGTTGA TTCCCCTTCT GAATGTCTCC 2640
TCATTCTGAC CTCCTCCTTC TCACACCCAC TGCCCTCCAC CCAGCCTGGC CTCAGCCCAG 2700
AAGGGCCTCC TCTCCAGCCT CCGTCCGGGT CTCTGTCACC TCACCTGTAC TCTGCCCTCC 2760
ACCTCACCTC TACTCTGCCC TCCGCCTCCC TCTGGAAGGC TGCTGTCCTC CTCCGGGGTC 2820
CTTCACTGCT 2830
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