| Tag | Content |
|---|
EnhancerAtlas ID | HS133-27614 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:159273190-159276010 |
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 | | TCF3 | MA0522.2 | chr6:159273513-159273523 | AACACCTGCT | + | 6.02 |
|
| | 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 | AACATTTTTG GATGAACTTT GTCTCTCAGG TTTTGGAGAA TTAAAATGCC TCCCTTATCC 60
CATCCCTGCC ACACTCTAGG ACATTGATTC ATGTTCCCAA AGAATAATGG TTAGCTTACT 120
GTATGCCAGC TACTATTCTT AGCTCCTTAC ATGAACTAAT CCTTTTAATC CTCACAACTA 180
CACTATGAAG CGGATGCTAC TATTGTCCAC TTTATGGGGG AAGAAACTGA GGCACAGAGA 240
GGTTAGCTTG CCTCGGGACT CTGTCTCTGC TGAGATTGGA AGCAGAAGAC TAGTTCCAGA 300
ATTCACACTC CTAACCCTAC TACAACACCT GCTCTCAAAC AGAGAAGGGA AAGGAAGTCC 360
TGGCGTTTGC ACTCTCCTTG ATCTTGTGCT GGTCTGGTCT GGACATGGAC CAAGGCTTGG 420
GGGCCTTGCA CACGTAAGTG AGTGCAGATG CCCGGCCCAG CCCCAGGGCT CCCTTGTCCT 480
TGAGCTGGGG CCACGCTGAG GCTGAGGCTG GCCTCCATGG CTTGACTTGA GGCCACCTCC 540
AGATCCACAC CCTGAAAGCT TGGGACTGGC CTTCTCAGAG AATGGGGCAA AACACTCTGA 600
CGCCAACTAC AACCATCACA AGGAGGTACA TTCTCTGTAA GGGCAAGCCT GGGGCTGCAC 660
CCAAGTAGAC TAGCAGACAC TCATTACAGA GAGAATGTTC TGGCACTCTG GCCCTGCCAA 720
AGGCTACCAG AACACAGAAG GCCCTTTCTT CCAAGGGGCC GAAGGAGGAG CAGGCACACA 780
CCATATGCCT CACTCACCAC ACGAAACCAC ACACCACATA GCACACACGC GTGCACCCTC 840
ATACCACACT GACCCTTCAC CACACACACA CCCATACACC TTCATGTCAC ACATACCACA 900
CACACAGATA TACCACATGC ACCCCATACA CCCCACCACA CACATACAAA CACCACACCA 960
TATACACACA CACACAGTAC AACATACACA CTCACACACC ATATGCCACA CACATATACT 1020
TTACACATAT ACATACCTCC AAACACACAC CATGCACACA CACGGTACAC CATACACACA 1080
CCACACACTA TGCACACACC ATGTACCACA CACATACCCC TCCAACATCA CATGAACACT 1140
ACGCACCCTC CCCCATACCA CACACATACA CGCACACGTA CCATGCACGC ACACACACCA 1200
CAATGTGCTG TTACTTAACA GGTTTGCCTT CCCACAACTC TATCAGCAAA CCCTTCTGGA 1260
GGCGCAGCCC ACACCTGCAT TCCAAAGAAC GCAAATCCCT TCCCTGCCCG ATGAAAGGCC 1320
CCTCCCACAG TGAGTCACAG AAACTGCAGC CGAGCAGGCA GTGGTGGGCC CCACCCTTCT 1380
CACAGGAAGT GAGAAAGAGT AAATATGTAG TTTTTCTTTG AGGGCCAATG CACATGTTAA 1440
ATGGGTGATT AAGAAGACAG AGAGCTGCTT AAAAGGTCAT GGGAGAAGTA CAATGTCTGG 1500
GGACTTGGCA GTAGCCTGGC AGAGACCGCA GGAATCCTAT AGAGTCTTTT ATGGACAGGG 1560
CTCTGAAATT CCAGAGCCTG CAGGAGGTAC CTTCCCCTTT GACTCGGCGG GGCTGTACCA 1620
CTAAGAATGC ACTGAGCATT GGGTGCACTT GGGATACCTG AGCTGTGGGG CCAGAGAGGC 1680
AGCCCTAGGG GAGAATTCCG GAGTTGGGGC TGGGTTCTTT CAGCATAAAA AATCAAAGTG 1740
TCGCTTCTTT AATGAACCTC CCGGCAAGGT CTTCCCTGAA GACCTTGAAC AAGTGTTCTT 1800
AAACAAGTGT TCCTTTATGC AATTAAAGGC CAGGGAAGCT GGGGTCTGAG AGGCCATGGA 1860
GCCATTGGGA TAATAGTGAC AGTTCGGCTA CCATTCAACT GGGCTTCTGA TGAATCATGC 1920
TGGGGGCAAG GACTCCAAAT CACCAGCTCT ACTCTATACT CGAATCAGTA GGCAGTTCAG 1980
ACAGTCTTGG GGGATTTGGG CAAACGAACG CTCCACTTAG AATCTCTCCA GAAAGACAAA 2040
GGGGGTGCCT AACAAACAAT TCAAGGACTG TGGGAAACCA ATGATCATCA AGGGCTCAGT 2100
TGTACAGTGT AAACCAAAAA GTATCTGAGA CAGGTCTCAA TCAACTGAGA AGTTTATTTT 2160
GCCAAGGTTA AGGACAGGCC AGGGAGGAAG AAACACGGAA TCACAGAAAC AGTCTATGGT 2220
CTGTGTCGTT CTTCCAAGAT GATGTTGAGG GCCTCGATGT TTAAAAGGGA AAAGTGGGCT 2280
GGAGAGGAAA GAGGAAGGGC ATGGGAATCT ACTTGTTGCA AGGGAAAAGG AGCAGGAAGA 2340
GGAACAATCA GTTACGTTTC CTCTAGCAGT CTGTAAATTG GTGCTTTACA TAAGATGAGC 2400
ATAGAGTTTA GCTGCCTGTG GTGGGGATAT CTAGCCTTTT ATCTGTAGCT ATCTGCTTAG 2460
GCACAAACAG AAAGGCAGCT TCTTGCATGA CTCAGCTTCT AGTTTAATTT TTTCCTGTTG 2520
CCAAGAAAAA ACTGGGGTCC TGAGAGTTTT TCTTTTCCTT TCACAACAGG AAGAAACAAA 2580
CTACAGAGCC CCTAGGTATA CTGGGGCCAC CTGGGGTCTT GTTAAAAATG TGCATTTGGG 2640
GGAGGGGCGG AGAGTCTGCG TTCCCCCCAT GCAGTGCCCA GGCTGCTGCT CTGTAGGCCA 2700
CACTTTGAAT ACTGAGAGTA CCAGAGAGGA CTTGGTGGTA GGGGGTGGTG GGTGGATTCT 2760
GGTACAGTTG GAGGGAGGAG GCTTCCTGGG GTGAGGGCAC TGAGATGGGT CCTGGTGGTA 2820
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