| Tag | Content |
|---|
EnhancerAtlas ID | HS032-00885 |
Organism | Homo sapiens |
Tissue/cell | DLD1 |
Coordinate | chr6:159273240-159276280 |
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: 2 | Chromosome | Start | End |
| chr6 | 159273399 | 159276272 | | chr6 | 159273925 | 159274893 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I158847 | chr6 | 159268541 | 159279766 |
|
Enhancer Sequence | TCCCTTATCC CATCCCTGCC ACACTCTAGG ACATTGATTC ATGTTCCCAA AGAATAATGG 60
TTAGCTTACT GTATGCCAGC TACTATTCTT AGCTCCTTAC ATGAACTAAT CCTTTTAATC 120
CTCACAACTA CACTATGAAG CGGATGCTAC TATTGTCCAC TTTATGGGGG AAGAAACTGA 180
GGCACAGAGA GGTTAGCTTG CCTCGGGACT CTGTCTCTGC TGAGATTGGA AGCAGAAGAC 240
TAGTTCCAGA ATTCACACTC CTAACCCTAC TACAACACCT GCTCTCAAAC AGAGAAGGGA 300
AAGGAAGTCC TGGCGTTTGC ACTCTCCTTG ATCTTGTGCT GGTCTGGTCT GGACATGGAC 360
CAAGGCTTGG GGGCCTTGCA CACGTAAGTG AGTGCAGATG CCCGGCCCAG CCCCAGGGCT 420
CCCTTGTCCT TGAGCTGGGG CCACGCTGAG GCTGAGGCTG GCCTCCATGG CTTGACTTGA 480
GGCCACCTCC AGATCCACAC CCTGAAAGCT TGGGACTGGC CTTCTCAGAG AATGGGGCAA 540
AACACTCTGA CGCCAACTAC AACCATCACA AGGAGGTACA TTCTCTGTAA GGGCAAGCCT 600
GGGGCTGCAC CCAAGTAGAC TAGCAGACAC TCATTACAGA GAGAATGTTC TGGCACTCTG 660
GCCCTGCCAA AGGCTACCAG AACACAGAAG GCCCTTTCTT CCAAGGGGCC GAAGGAGGAG 720
CAGGCACACA CCATATGCCT CACTCACCAC ACGAAACCAC ACACCACATA GCACACACGC 780
GTGCACCCTC ATACCACACT GACCCTTCAC CACACACACA CCCATACACC TTCATGTCAC 840
ACATACCACA CACACAGATA TACCACATGC ACCCCATACA CCCCACCACA CACATACAAA 900
CACCACACCA TATACACACA CACACAGTAC AACATACACA CTCACACACC ATATGCCACA 960
CACATATACT TTACACATAT ACATACCTCC AAACACACAC CATGCACACA CACGGTACAC 1020
CATACACACA CCACACACTA TGCACACACC ATGTACCACA CACATACCCC TCCAACATCA 1080
CATGAACACT ACGCACCCTC CCCCATACCA CACACATACA CGCACACGTA CCATGCACGC 1140
ACACACACCA CAATGTGCTG TTACTTAACA GGTTTGCCTT CCCACAACTC TATCAGCAAA 1200
CCCTTCTGGA GGCGCAGCCC ACACCTGCAT TCCAAAGAAC GCAAATCCCT TCCCTGCCCG 1260
ATGAAAGGCC CCTCCCACAG TGAGTCACAG AAACTGCAGC CGAGCAGGCA GTGGTGGGCC 1320
CCACCCTTCT CACAGGAAGT GAGAAAGAGT AAATATGTAG TTTTTCTTTG AGGGCCAATG 1380
CACATGTTAA ATGGGTGATT AAGAAGACAG AGAGCTGCTT AAAAGGTCAT GGGAGAAGTA 1440
CAATGTCTGG GGACTTGGCA GTAGCCTGGC AGAGACCGCA GGAATCCTAT AGAGTCTTTT 1500
ATGGACAGGG CTCTGAAATT CCAGAGCCTG CAGGAGGTAC CTTCCCCTTT GACTCGGCGG 1560
GGCTGTACCA CTAAGAATGC ACTGAGCATT GGGTGCACTT GGGATACCTG AGCTGTGGGG 1620
CCAGAGAGGC AGCCCTAGGG GAGAATTCCG GAGTTGGGGC TGGGTTCTTT CAGCATAAAA 1680
AATCAAAGTG TCGCTTCTTT AATGAACCTC CCGGCAAGGT CTTCCCTGAA GACCTTGAAC 1740
AAGTGTTCTT AAACAAGTGT TCCTTTATGC AATTAAAGGC CAGGGAAGCT GGGGTCTGAG 1800
AGGCCATGGA GCCATTGGGA TAATAGTGAC AGTTCGGCTA CCATTCAACT GGGCTTCTGA 1860
TGAATCATGC TGGGGGCAAG GACTCCAAAT CACCAGCTCT ACTCTATACT CGAATCAGTA 1920
GGCAGTTCAG ACAGTCTTGG GGGATTTGGG CAAACGAACG CTCCACTTAG AATCTCTCCA 1980
GAAAGACAAA GGGGGTGCCT AACAAACAAT TCAAGGACTG TGGGAAACCA ATGATCATCA 2040
AGGGCTCAGT TGTACAGTGT AAACCAAAAA GTATCTGAGA CAGGTCTCAA TCAACTGAGA 2100
AGTTTATTTT GCCAAGGTTA AGGACAGGCC AGGGAGGAAG AAACACGGAA TCACAGAAAC 2160
AGTCTATGGT CTGTGTCGTT CTTCCAAGAT GATGTTGAGG GCCTCGATGT TTAAAAGGGA 2220
AAAGTGGGCT GGAGAGGAAA GAGGAAGGGC ATGGGAATCT ACTTGTTGCA AGGGAAAAGG 2280
AGCAGGAAGA GGAACAATCA GTTACGTTTC CTCTAGCAGT CTGTAAATTG GTGCTTTACA 2340
TAAGATGAGC ATAGAGTTTA GCTGCCTGTG GTGGGGATAT CTAGCCTTTT ATCTGTAGCT 2400
ATCTGCTTAG GCACAAACAG AAAGGCAGCT TCTTGCATGA CTCAGCTTCT AGTTTAATTT 2460
TTTCCTGTTG CCAAGAAAAA ACTGGGGTCC TGAGAGTTTT TCTTTTCCTT TCACAACAGG 2520
AAGAAACAAA CTACAGAGCC CCTAGGTATA CTGGGGCCAC CTGGGGTCTT GTTAAAAATG 2580
TGCATTTGGG GGAGGGGCGG AGAGTCTGCG TTCCCCCCAT GCAGTGCCCA GGCTGCTGCT 2640
CTGTAGGCCA CACTTTGAAT ACTGAGAGTA CCAGAGAGGA CTTGGTGGTA GGGGGTGGTG 2700
GGTGGATTCT GGTACAGTTG GAGGGAGGAG GCTTCCTGGG GTGAGGGCAC TGAGATGGGT 2760
CCTGGTGGTA AGATTGTGTG GGGAGGAGAA TAAAGGTACC CCAGATCAAC CTTGTGGGGC 2820
AACAAGTGAC CTGACAAACT CCCATCATGT ATGGCCACTG TCCCCCATTC AAGGCCAGGG 2880
ACCGTTGGAG GAGTTGGAAA GTTAAGAGCT TGAAAACTGG ATTCTGCCTC ACTGGGAGGT 2940
TCACTGACAT TTAGTCTTCT CTGAAAGATG GGCATAGTTA TACCAATCCT ACAGGAGTAG 3000
TGTGAAGATT AAATGAGATG ACATATAAAG TGCTTAGGGC 3040
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