| Tag | Content |
|---|
EnhancerAtlas ID | HS151-00595 |
Organism | Homo sapiens |
Tissue/cell | OCI-LY1 |
Coordinate | chr1:111761280-111763760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MIXL1 | MA0662.1 | chr1:111763500-111763510 | TCTAATTAAC | + | 6.02 |
|
| | Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
| SE_09820 | chr1:111761643-111766110 | CD14 | | SE_10666 | chr1:111761171-111766634 | CD19_Primary | | SE_11981 | chr1:111761208-111763781 | CD3 | | SE_14851 | chr1:111761268-111763705 | CD4_Memory_Primary_7pool | | SE_15989 | chr1:111761692-111763714 | CD4_Naive_Primary_7pool | | SE_16482 | chr1:111761494-111763515 | CD4_Naive_Primary_8pool | | SE_17180 | chr1:111761880-111762489 | CD4p_CD225int_CD127p_Tmem | | SE_17406 | chr1:111754232-111773369 | CD4p_CD25-_CD45RAp_Naive | | SE_17935 | chr1:111756443-111766770 | CD4p_CD25-_CD45ROp_Memory | | SE_18363 | chr1:111754958-111773351 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19522 | chr1:111761621-111766456 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20205 | chr1:111756283-111766729 | CD56 | | SE_22036 | chr1:111756151-111766467 | CD8_Naive_8pool | | SE_22415 | chr1:111756175-111771793 | CD8_primiary | | SE_25351 | chr1:111754260-111776321 | DND41 | | SE_30932 | chr1:111761210-111772142 | Fetal_Thymus | | SE_32464 | chr1:111755211-111769514 | GM12878 | | SE_39435 | chr1:111761540-111763899 | Jurkat | | SE_50246 | chr1:111761490-111766358 | Sigmoid_Colon | | SE_52868 | chr1:111761530-111763557 | Small_Intestine | | SE_53613 | chr1:111761416-111766494 | Spleen | | SE_55120 | chr1:111761566-111766429 | Thymus | | SE_58401 | chr1:111735195-111775083 | Ly1 | | SE_59710 | chr1:111743394-111766646 | Ly4 | | SE_60497 | chr1:111739632-111775084 | DHL6 | | SE_61322 | chr1:111744674-111766741 | HBL1 | | SE_62234 | chr1:111732684-111775273 | Tonsil | | SE_66284 | chr1:111761540-111763899 | Jurkat |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 111762030 | 111762790 | | chr1 | 111762260 | 111762740 |
|
Enhancer Sequence | GATTCGCCTG CCTCGACCTC CCAAAGTGCT GAGATTACAG GTGTGAGCCA CCGTGCCTGG 60
TTTTGAACAT ACTTATAATA GCTGCTTTAA AGGTCTTGTA TATTAATATC TGTCATTTCT 120
AGATCTGTTT CTATTGACAC ATTTTTCTCC TGGTTATAAG TCACATTTCC TGTTTTTTGG 180
TATATCTAGT GATTTTTTTT TTAATTGGAT GCTTGACATT ATAAATGTTA TGTTGCTGTT 240
GAATGTTTAG ATTTTGTGGC CAGGAAGTCA ATTTATTTGG AGATTGACAA GAGCTTTTTT 300
TTTTTTTTTT AGACAAGGTC TTATTCTGTT GCCCAGGCTG GCGTGCAGTG GTGTGATCAT 360
AGCTCACAGT AGCTTCGACC TCCTGGGCAC AAACAATCCT CCTGCCTTAG CCTCTCAAGT 420
AGCTGGGACT ACAGGTGTAT GCCACTATGA CCAAATAATT ATTTAAATTT TTTTTTGTAA 480
AGACAGAGTC TCTATGCCGC TGAGGCTGGT CACAGACTCC TGGCCTCCAG CAGTCCTCCC 540
ACCTCGGCCT CCCAAGGTGC TGGGATTACA AGTGTGAGCC ACTGTGCCCC GCTCAACTTG 600
AACATTTTGA AGCTTGTGTT TAAACTTTGT TAGAACAAGT CTAGAGTCAC CCTTACCATG 660
GGGCTAGTGA GGCCCTTAAC TAAAGTTTGA CGCTTCTGAG GTTTCTATTA AATTTCCAGC 720
TGCTCAAGAA GGACTTTCCA CTCTAGCCGG TCTTATCAAA TGTCTCCCAG CCCAGTGCAA 780
GCTTTAGTGG TTGTTCAGCT TCCAGATCTC TGGTGGTGCT TATTTCCTTG GTACTTTTGG 840
TTGTTGTTGT TTTTGCCCAT TCTGCTGTAG TCTCACCCTC TGTATGAGAG CTTTGTATTC 900
AGCCACAGAT CTGAGAGAAC CCCATGCAGG TTTCTGAAGC TCTTTTTCTG TACTGCTCCC 960
TTATCTCTGG CATTCTATTG TGAAGTTTCC AAGCCTCTCA GCCTCTTCAA ACTCCATTCT 1020
TTGTCTCAGT GGGACTTGCA TGCTCTCCAT AGGCCCCCCT CCTTGTGTTG CAGTCTGCAC 1080
AAGGCACAGT TGTGGGAGGG CTCACCTCAT TTGTTTTCAC AGCCCTGCAT TGCATGTTGC 1140
CTAATGTATG AAAACAATCA TTCTGTATAT TTTATATCAT ATTCTAGTTT ACCGTGTGAG 1200
AGTTACTCAG TCGTTACTGG AGGAGGCCAC AAATACTTAT TAAACGTGTG AAGTATTTTA 1260
GTTTCCATGC TGGTTAGTAG GCTGTGAAGA TGAGTTAGTG TGCATAGAGG AGGTAGAGGA 1320
TGTGAAACTC AGGGTGGGTG GGTGAGGAGG AATTTGCCCA AGACAAAGCT ATTGTTAGAC 1380
CTAGGAGGAG AGGCCTGGTG CTTTGCATCC TCGGGCTGTG CTTTCACACA CAAGCCACAT 1440
CATCTCTTCC CTGGCTTAGC TGCTCTGAGC ACTGCCTCCT CCTCAGTCGT CTCCTCCTCT 1500
TCAGTTATGT CTTCCAGCAT TTGGGATGCT GACTTCTTCA GCCAAGCCCC CTCCAAGCCC 1560
TCCCCATACC CACATTCAGA TAAAGTGGAA AGAGGTTTTC TATCCCAAGT GTATCAGATC 1620
ATTTGGAAAG ATCAAGACCC ACTAGCTCCA TCATGAGCCA GTGGATGAGC TTTCTGATTG 1680
TCCCTGCTTT GACTCCCACT TCCGATTTGC CCAAAGCCCC TCTCACCACC ATGCAGCCTG 1740
CAATATGAGA CCATGTCTGT GAAACCGTGC CATGAACAGC AACACTTAAG GAAATTGGAT 1800
TATTTAATCA ATAATTGGAG CAATAAGCAT CTGCCTCGGT GTGCCAGGCC ACAAGAGGCA 1860
CAGGTAAAAG GCCTGTCTTC TCAAGAAGCA CTTATTCTAG AGACTGGCTG CCCACTGTGG 1920
GGTTCAGTTA GCAGAAAACA CCCTGCTGCC AGTGGTTTCA GGGTCTGCCT CAGGTGCAGA 1980
TAAGGCAAAG GATCCCTTTG CCCAAGGTCA TGACTTACCA GGGAAGCCCA TCACTTGTGG 2040
CTGAATGAGG AGGGCGTATA AAGACCCAGG CATTTTAGTC TGAAGTGAGG CAACTCTGAT 2100
GGACGTCACT TCTTCTGAAT CTCATGGCTA GGTTGGCTGA AGCTTTGTCG GAGCTGCATC 2160
CAAACTCAGC CTCTTCCTCT GCCCAATCTT GCTCCCTCTT TCCTTTCACA ACAGATAATT 2220
TCTAATTAAC AGCTTGTGCC CACACTTCAA TTCCACACCT GCTTCTAGGG GGCCCAACTC 2280
GTGACACAGG GAATGGCCGT GACCATGGGC TTTGGCAGCT ACAGTCCAGT CCACTTTCCC 2340
TGCAGACAGG GAAAGGTCAG GTCAGGCAGG GGATGATGAC TCCACAGAAG AGTCACCCTG 2400
ATACCACAGG CTTCAGCTTC TCAACACTTT TTACCTCCCT TCTTTTTTTT TTTTTTTTTT 2460
TTTTGAGATA GAGTCTTGCT 2480
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