| Tag | Content |
|---|
EnhancerAtlas ID | HS127-27991 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr6:159273740-159276500 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr6:159274110-159274130 | ACCCCATACACCCCACCACA | + | 6.14 | | RREB1 | MA0073.1 | chr6:159275925-159275945 | TGGTAGGGGGTGGTGGGTGG | - | 7.57 |
|
| | Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
| SE_10307 | chr6:159273179-159276502 | CD19_Primary | | SE_11101 | chr6:159269935-159278161 | CD20 | | SE_12189 | chr6:159273267-159276491 | CD3 | | SE_14386 | chr6:159269967-159276559 | CD4_Memory_Primary_7pool | | SE_16462 | chr6:159273351-159276594 | CD4_Naive_Primary_8pool | | SE_17999 | chr6:159269964-159278117 | CD4p_CD25-_CD45ROp_Memory | | SE_18987 | chr6:159273136-159277721 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_20282 | chr6:159273082-159276574 | CD56 | | SE_20897 | chr6:159272786-159276642 | CD8_Memory_7pool | | SE_21904 | chr6:159273108-159276540 | CD8_Naive_7pool | | SE_22378 | chr6:159270210-159277819 | CD8_primiary | | SE_23109 | chr6:159273079-159276256 | Colon_Crypt_1 | | SE_23789 | chr6:159273267-159275641 | Colon_Crypt_2 | | SE_23789 | chr6:159275700-159276183 | Colon_Crypt_2 | | SE_25058 | chr6:159273048-159276283 | Colon_Crypt_3 | | SE_27140 | chr6:159273240-159276220 | Esophagus | | SE_27853 | chr6:159268889-159276361 | Fetal_Intestine | | SE_28795 | chr6:159268853-159276331 | Fetal_Intestine_Large | | SE_34137 | chr6:159273141-159276469 | HCC1954 | | SE_34397 | chr6:159270023-159277893 | HCT-116 | | SE_34769 | chr6:159269432-159276667 | HeLa | | SE_35994 | chr6:159268630-159276489 | HMEC | | SE_40070 | chr6:159273143-159276574 | K562 | | SE_51056 | chr6:159273219-159276293 | Sigmoid_Colon | | SE_52705 | chr6:159273298-159276322 | Small_Intestine | | SE_58403 | chr6:159210147-159292283 | Ly1 | | SE_63169 | chr6:159270185-159292330 | Tonsil | | SE_64395 | chr6:159270254-159276320 | NHEK | | SE_69169 | chr6:159273396-159276424 | 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 |
| GH06I158847 | chr6 | 159268541 | 159279766 |
|
Enhancer Sequence | CCTGAAAGCT TGGGACTGGC CTTCTCAGAG AATGGGGCAA AACACTCTGA CGCCAACTAC 60
AACCATCACA AGGAGGTACA TTCTCTGTAA GGGCAAGCCT GGGGCTGCAC CCAAGTAGAC 120
TAGCAGACAC TCATTACAGA GAGAATGTTC TGGCACTCTG GCCCTGCCAA AGGCTACCAG 180
AACACAGAAG GCCCTTTCTT CCAAGGGGCC GAAGGAGGAG CAGGCACACA CCATATGCCT 240
CACTCACCAC ACGAAACCAC ACACCACATA GCACACACGC GTGCACCCTC ATACCACACT 300
GACCCTTCAC CACACACACA CCCATACACC TTCATGTCAC ACATACCACA CACACAGATA 360
TACCACATGC ACCCCATACA CCCCACCACA CACATACAAA CACCACACCA TATACACACA 420
CACACAGTAC AACATACACA CTCACACACC ATATGCCACA CACATATACT TTACACATAT 480
ACATACCTCC AAACACACAC CATGCACACA CACGGTACAC CATACACACA CCACACACTA 540
TGCACACACC ATGTACCACA CACATACCCC TCCAACATCA CATGAACACT ACGCACCCTC 600
CCCCATACCA CACACATACA CGCACACGTA CCATGCACGC ACACACACCA CAATGTGCTG 660
TTACTTAACA GGTTTGCCTT CCCACAACTC TATCAGCAAA CCCTTCTGGA GGCGCAGCCC 720
ACACCTGCAT TCCAAAGAAC GCAAATCCCT TCCCTGCCCG ATGAAAGGCC CCTCCCACAG 780
TGAGTCACAG AAACTGCAGC CGAGCAGGCA GTGGTGGGCC CCACCCTTCT CACAGGAAGT 840
GAGAAAGAGT AAATATGTAG TTTTTCTTTG AGGGCCAATG CACATGTTAA ATGGGTGATT 900
AAGAAGACAG AGAGCTGCTT AAAAGGTCAT GGGAGAAGTA CAATGTCTGG GGACTTGGCA 960
GTAGCCTGGC AGAGACCGCA GGAATCCTAT AGAGTCTTTT ATGGACAGGG CTCTGAAATT 1020
CCAGAGCCTG CAGGAGGTAC CTTCCCCTTT GACTCGGCGG GGCTGTACCA CTAAGAATGC 1080
ACTGAGCATT GGGTGCACTT GGGATACCTG AGCTGTGGGG CCAGAGAGGC AGCCCTAGGG 1140
GAGAATTCCG GAGTTGGGGC TGGGTTCTTT CAGCATAAAA AATCAAAGTG TCGCTTCTTT 1200
AATGAACCTC CCGGCAAGGT CTTCCCTGAA GACCTTGAAC AAGTGTTCTT AAACAAGTGT 1260
TCCTTTATGC AATTAAAGGC CAGGGAAGCT GGGGTCTGAG AGGCCATGGA GCCATTGGGA 1320
TAATAGTGAC AGTTCGGCTA CCATTCAACT GGGCTTCTGA TGAATCATGC TGGGGGCAAG 1380
GACTCCAAAT CACCAGCTCT ACTCTATACT CGAATCAGTA GGCAGTTCAG ACAGTCTTGG 1440
GGGATTTGGG CAAACGAACG CTCCACTTAG AATCTCTCCA GAAAGACAAA GGGGGTGCCT 1500
AACAAACAAT TCAAGGACTG TGGGAAACCA ATGATCATCA AGGGCTCAGT TGTACAGTGT 1560
AAACCAAAAA GTATCTGAGA CAGGTCTCAA TCAACTGAGA AGTTTATTTT GCCAAGGTTA 1620
AGGACAGGCC AGGGAGGAAG AAACACGGAA TCACAGAAAC AGTCTATGGT CTGTGTCGTT 1680
CTTCCAAGAT GATGTTGAGG GCCTCGATGT TTAAAAGGGA AAAGTGGGCT GGAGAGGAAA 1740
GAGGAAGGGC ATGGGAATCT ACTTGTTGCA AGGGAAAAGG AGCAGGAAGA GGAACAATCA 1800
GTTACGTTTC CTCTAGCAGT CTGTAAATTG GTGCTTTACA TAAGATGAGC ATAGAGTTTA 1860
GCTGCCTGTG GTGGGGATAT CTAGCCTTTT ATCTGTAGCT ATCTGCTTAG GCACAAACAG 1920
AAAGGCAGCT TCTTGCATGA CTCAGCTTCT AGTTTAATTT TTTCCTGTTG CCAAGAAAAA 1980
ACTGGGGTCC TGAGAGTTTT TCTTTTCCTT TCACAACAGG AAGAAACAAA CTACAGAGCC 2040
CCTAGGTATA CTGGGGCCAC CTGGGGTCTT GTTAAAAATG TGCATTTGGG GGAGGGGCGG 2100
AGAGTCTGCG TTCCCCCCAT GCAGTGCCCA GGCTGCTGCT CTGTAGGCCA CACTTTGAAT 2160
ACTGAGAGTA CCAGAGAGGA CTTGGTGGTA GGGGGTGGTG GGTGGATTCT GGTACAGTTG 2220
GAGGGAGGAG GCTTCCTGGG GTGAGGGCAC TGAGATGGGT CCTGGTGGTA AGATTGTGTG 2280
GGGAGGAGAA TAAAGGTACC CCAGATCAAC CTTGTGGGGC AACAAGTGAC CTGACAAACT 2340
CCCATCATGT ATGGCCACTG TCCCCCATTC AAGGCCAGGG ACCGTTGGAG GAGTTGGAAA 2400
GTTAAGAGCT TGAAAACTGG ATTCTGCCTC ACTGGGAGGT TCACTGACAT TTAGTCTTCT 2460
CTGAAAGATG GGCATAGTTA TACCAATCCT ACAGGAGTAG TGTGAAGATT AAATGAGATG 2520
ACATATAAAG TGCTTAGGGC CTGGGGCAGC ATAAGTGGTA GAATATTTGT TCATATTATT 2580
ATTGTTATTA TTATTAGCTG AAGCAATTTT TTTTTTTTTG AGATGGAGTT TTGCTCTTCT 2640
TGCCCAAGCT GGAGTGCAGT GGCACGATCT TGGCTCACTG CAACCTCTGC CTCCCAGGTT 2700
CAAGCAATTC TCCTGTCTCA GCCTCCCAAG TAGCTGGGAT TACAGGTATG CGCCACCATG 2760
|
