| Tag | Content |
|---|
EnhancerAtlas ID | HS051-16762 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr2:232578250-232580460 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr2:232578694-232578713 | TGGCTCCCCCTGCTGGTGG | - | 6.79 | | CTCF | MA0139.1 | chr2:232580118-232580137 | GGGCGCCCCCTGGTGGACA | - | 8.28 |
|
| | Number of super-enhancer constituents: 38 | ID | Coordinate | Tissue/cell |
| SE_00956 | chr2:232578204-232579832 | Adrenal_Gland | | SE_01925 | chr2:232578253-232582413 | Aorta | | SE_02825 | chr2:232580113-232582812 | Astrocytes | | SE_03959 | chr2:232578056-232580822 | Brain_Anterior_Caudate | | SE_05842 | chr2:232577996-232582144 | Brain_Hippocampus_Middle | | SE_07044 | chr2:232578065-232580386 | Brain_Hippocampus_Middle_150 | | SE_09877 | chr2:232578067-232580073 | CD14 | | SE_10230 | chr2:232578106-232580150 | CD19_Primary | | SE_11186 | chr2:232577955-232583649 | CD20 | | SE_17449 | chr2:232578058-232580210 | CD4p_CD25-_CD45RAp_Naive | | SE_17954 | chr2:232577947-232580262 | CD4p_CD25-_CD45ROp_Memory | | SE_19298 | chr2:232578123-232580126 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20039 | chr2:232578094-232580376 | CD56 | | SE_23369 | chr2:232578230-232580096 | Colon_Crypt_1 | | SE_23858 | chr2:232578276-232580039 | Colon_Crypt_2 | | SE_29881 | chr2:232578146-232579287 | Fetal_Muscle | | SE_31203 | chr2:232578111-232580359 | Fetal_Thymus | | SE_31593 | chr2:232578213-232580151 | Gastric | | SE_34344 | chr2:232578068-232581794 | HCT-116 | | SE_40298 | chr2:232579861-232581466 | K562 | | SE_40898 | chr2:232578114-232580329 | Left_Ventricle | | SE_41878 | chr2:232578279-232580082 | LNCaP | | SE_42309 | chr2:232578184-232582081 | Lung | | SE_45367 | chr2:232578216-232578729 | NHLF | | SE_48320 | chr2:232578125-232579930 | Psoas_Muscle | | SE_48893 | chr2:232578236-232580346 | Right_Atrium | | SE_50294 | chr2:232578208-232580253 | Sigmoid_Colon | | SE_51193 | chr2:232578109-232579502 | Skeletal_Muscle | | SE_52558 | chr2:232578176-232580197 | Small_Intestine | | SE_53406 | chr2:232578123-232579503 | Spleen | | SE_54960 | chr2:232577999-232580171 | Stomach_Smooth_Muscle | | SE_55260 | chr2:232578226-232579185 | Thymus | | SE_55260 | chr2:232579316-232579753 | Thymus | | SE_60861 | chr2:232570521-232583361 | DHL6 | | SE_62367 | chr2:232570197-232583171 | Tonsil | | SE_65285 | chr2:232578039-232580905 | Pancreatic_islets | | SE_68671 | chr2:232570486-232579636 | TC71 | | SE_68763 | chr2:232578263-232580504 | H9 |
|
| | 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 |
| GH02I231713 | chr2 | 232578117 | 232582910 |
|
Enhancer Sequence | AGCTGTCTCA AGCCTGGTTT TTCTGTTTCA GTTTCTTCAG ACCTTCCAGG GCACAAGGAT 60
AGGAGGGGGA GGATCCTGGG GACAGTGGGT TGACATTTTG GGAGGCAGTT GGATGTGTCC 120
TGTGATGGGC AGCAGAGTCT GGTGGGTGGG CAGGGACTGA GCTGCAGTTG GCTGGGGGGG 180
CTGCTCACTG GGGCAGTCAG TGATTGCCCC AAGAAGCCTT AACTGGGGAG GAGGACTTCA 240
TCACTGGGTG CCACATGGGG ACCCTGGTGC CCTGGGGGTG GGGGTTTGCA GTCCTAGACA 300
CTGGAAACGG GCCACACGGG ACTGCCATTA TGTGGAGCGC AGGGTGCTGG TGGTATAGGC 360
CAAGAGGGAA CTTGCCAAGC CTCCCAGGAT GAGCGTCCAA GTGGTGGCTG CCTCTGCAGG 420
CCTCACAGGT TTAGCTCCAT GACGTGGCTC CCCCTGCTGG TGGCACGTGG TACCCCCCGG 480
CCTCTTAGAA TGCCGGGGTT TTGGTTTGGC ACTGGTGCAG CCTGGCAGTC ATCCAACCTT 540
TGGTCTCCAG GTCCCTTAGG TTAGTTGGGC AGGCCCACCC TGCCCCTTGA ACACAGTTGG 600
AGAAGTTACT GTGCCGTTTG GATATTCATA CACGGGCTGT GAGCAGTGGG TCAGGATAGC 660
CAACTGGAGG AAGTGCCACC AGCTCGTGCC CTCAGAGGTG GAGGTAAGGA TTAGAGCTCA 720
CCTAGAACCT TCTGGGATCC TCCAATGAGA GCTGCAGGGG CAGGGGCCGG TATAGGCACT 780
GCTAGTGGGC CTGTTGCCCA GGTAGGACCT GAGGAAGCCA TCCAGTGGTA TCTGCAGGAA 840
AACTCCCAGG AGCAGACTGA AGTGTCTGCA GAGGCCTGGC CTGGGTTAAG GGGAGATGCT 900
GGGAAGGAGG GAAATGTGTG CATTGAAGAG AGCAAGAGAG ACCAGTTCCC TCTACCTGCC 960
CCTTGACACC GTGTCCACCC CATTCCATGC CCCCCCGACC TTTGTGTTTC ACACCAGGCA 1020
CCAGAGTTCT GGGGGGACCT TTCCCTTCTC TGGCTGGAGC TTAGTCACTC TCATGGGGCT 1080
GCTCAGGCCG CTTGTTCAGC ATGTCCCCAG GCAGCTGCCA CCAGGATCGG GGGCAGGTTG 1140
AGGCCTTGGT AGGAGGGACC CTCTGACCTG TATCTACCCC ACACCCCCTG CACAGCCTGG 1200
GTATCTGCAT CCTGGCTCAT CCAGGGAAGA AAGGGAGGGT CTGGAGCCAA AACGCTGGCT 1260
CCTCTCTGTT CTGCCGCCCA AGGCGACTCA GTACTGCAGT GTTCCCAAGC TCGGCGCCCA 1320
GGAGGGTGTC TCTAAGGCAG GAGTGCAGGC GAAGGCCGTG AAGGAAGGCC ACACAGGGCA 1380
GGTAGCGCTT GGAGCTGAGA GCAGATCTAA CCCAGCTCCC TCAGGCTGCA GTCCTGCTCG 1440
GGACCACTAC CGCAAGGCCC CTGAAAGGGG AGAAGCTGTG CCCTGGTCCG CACACAGACA 1500
CGGCAGGCAT GTTAGCATGA GGCAAGTAAC TGAACCTTGT GGGCTTCAAT CCCCTCCTCT 1560
GCAAAATGGG AACAATAGGA TGAGGCATGA GCCAGGGCCC AGGGCTGCCT TGCTAGGGTC 1620
CCCCTGAGAC ACCCATATCA GCAGAGCTTA CTGCCTCTGC TGTCTGAGCT GCCTCATCCC 1680
ACCAAAGGTT TGGCCTGGAA CAGCATTTGC TGGTTCTAGC AGAACACACT TACCCCTAGT 1740
CCTGAGCCTA GCACACAATT AACCACTGCC TGAGGATATA CCTCAGGGCC CAGAGTCACC 1800
TTGATACCAC TCCCAAAGTC CCCGAATGAC CTCCCACTGG AGCCCAGGTT AAAAGATTAT 1860
CAAGGAATGG GCGCCCCCTG GTGGACACAG AGGAACTGTA AAGCGTGCCG CTGAATTCTG 1920
TCCAGGAAAG ACCCTTCAGT GGGCCCTGGT CCCAAGGTAG GCAACGCCAG TCACCCTCCA 1980
CCTGACTCCC GCAACAAGAC CTTTCTCCCT CTCTGTTGCT GGAACCCCAG TCAGATGTGA 2040
CAGTCAGTGG TCATTTCCCA GACCTTCCTT CTGGGCAACT GATGCCCTCT CCCAAGGACT 2100
GAGTCCTTTA CGTGGAACCA AAGCTGGAAG CAGGGGTCCA CTCTTCCACG GTCTTGGGCT 2160
TCCCTGTGGC CACACACACC CTCACTGGAC TCCACGCACC CTCACTGGAC 2210
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