| Tag | Content |
|---|
EnhancerAtlas ID | HS031-20977 |
Organism | Homo sapiens |
Tissue/cell | Denditric_cell |
Coordinate | chr6:159273250-159276210 |
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 | CATCCCTGCC ACACTCTAGG ACATTGATTC ATGTTCCCAA AGAATAATGG TTAGCTTACT 60
GTATGCCAGC TACTATTCTT AGCTCCTTAC ATGAACTAAT CCTTTTAATC CTCACAACTA 120
CACTATGAAG CGGATGCTAC TATTGTCCAC TTTATGGGGG AAGAAACTGA GGCACAGAGA 180
GGTTAGCTTG CCTCGGGACT CTGTCTCTGC TGAGATTGGA AGCAGAAGAC TAGTTCCAGA 240
ATTCACACTC CTAACCCTAC TACAACACCT GCTCTCAAAC AGAGAAGGGA AAGGAAGTCC 300
TGGCGTTTGC ACTCTCCTTG ATCTTGTGCT GGTCTGGTCT GGACATGGAC CAAGGCTTGG 360
GGGCCTTGCA CACGTAAGTG AGTGCAGATG CCCGGCCCAG CCCCAGGGCT CCCTTGTCCT 420
TGAGCTGGGG CCACGCTGAG GCTGAGGCTG GCCTCCATGG CTTGACTTGA GGCCACCTCC 480
AGATCCACAC CCTGAAAGCT TGGGACTGGC CTTCTCAGAG AATGGGGCAA AACACTCTGA 540
CGCCAACTAC AACCATCACA AGGAGGTACA TTCTCTGTAA GGGCAAGCCT GGGGCTGCAC 600
CCAAGTAGAC TAGCAGACAC TCATTACAGA GAGAATGTTC TGGCACTCTG GCCCTGCCAA 660
AGGCTACCAG AACACAGAAG GCCCTTTCTT CCAAGGGGCC GAAGGAGGAG CAGGCACACA 720
CCATATGCCT CACTCACCAC ACGAAACCAC ACACCACATA GCACACACGC GTGCACCCTC 780
ATACCACACT GACCCTTCAC CACACACACA CCCATACACC TTCATGTCAC ACATACCACA 840
CACACAGATA TACCACATGC ACCCCATACA CCCCACCACA CACATACAAA CACCACACCA 900
TATACACACA CACACAGTAC AACATACACA CTCACACACC ATATGCCACA CACATATACT 960
TTACACATAT ACATACCTCC AAACACACAC CATGCACACA CACGGTACAC CATACACACA 1020
CCACACACTA TGCACACACC ATGTACCACA CACATACCCC TCCAACATCA CATGAACACT 1080
ACGCACCCTC CCCCATACCA CACACATACA CGCACACGTA CCATGCACGC ACACACACCA 1140
CAATGTGCTG TTACTTAACA GGTTTGCCTT CCCACAACTC TATCAGCAAA CCCTTCTGGA 1200
GGCGCAGCCC ACACCTGCAT TCCAAAGAAC GCAAATCCCT TCCCTGCCCG ATGAAAGGCC 1260
CCTCCCACAG TGAGTCACAG AAACTGCAGC CGAGCAGGCA GTGGTGGGCC CCACCCTTCT 1320
CACAGGAAGT GAGAAAGAGT AAATATGTAG TTTTTCTTTG AGGGCCAATG CACATGTTAA 1380
ATGGGTGATT AAGAAGACAG AGAGCTGCTT AAAAGGTCAT GGGAGAAGTA CAATGTCTGG 1440
GGACTTGGCA GTAGCCTGGC AGAGACCGCA GGAATCCTAT AGAGTCTTTT ATGGACAGGG 1500
CTCTGAAATT CCAGAGCCTG CAGGAGGTAC CTTCCCCTTT GACTCGGCGG GGCTGTACCA 1560
CTAAGAATGC ACTGAGCATT GGGTGCACTT GGGATACCTG AGCTGTGGGG CCAGAGAGGC 1620
AGCCCTAGGG GAGAATTCCG GAGTTGGGGC TGGGTTCTTT CAGCATAAAA AATCAAAGTG 1680
TCGCTTCTTT AATGAACCTC CCGGCAAGGT CTTCCCTGAA GACCTTGAAC AAGTGTTCTT 1740
AAACAAGTGT TCCTTTATGC AATTAAAGGC CAGGGAAGCT GGGGTCTGAG AGGCCATGGA 1800
GCCATTGGGA TAATAGTGAC AGTTCGGCTA CCATTCAACT GGGCTTCTGA TGAATCATGC 1860
TGGGGGCAAG GACTCCAAAT CACCAGCTCT ACTCTATACT CGAATCAGTA GGCAGTTCAG 1920
ACAGTCTTGG GGGATTTGGG CAAACGAACG CTCCACTTAG AATCTCTCCA GAAAGACAAA 1980
GGGGGTGCCT AACAAACAAT TCAAGGACTG TGGGAAACCA ATGATCATCA AGGGCTCAGT 2040
TGTACAGTGT AAACCAAAAA GTATCTGAGA CAGGTCTCAA TCAACTGAGA AGTTTATTTT 2100
GCCAAGGTTA AGGACAGGCC AGGGAGGAAG AAACACGGAA TCACAGAAAC AGTCTATGGT 2160
CTGTGTCGTT CTTCCAAGAT GATGTTGAGG GCCTCGATGT TTAAAAGGGA AAAGTGGGCT 2220
GGAGAGGAAA GAGGAAGGGC ATGGGAATCT ACTTGTTGCA AGGGAAAAGG AGCAGGAAGA 2280
GGAACAATCA GTTACGTTTC CTCTAGCAGT CTGTAAATTG GTGCTTTACA TAAGATGAGC 2340
ATAGAGTTTA GCTGCCTGTG GTGGGGATAT CTAGCCTTTT ATCTGTAGCT ATCTGCTTAG 2400
GCACAAACAG AAAGGCAGCT TCTTGCATGA CTCAGCTTCT AGTTTAATTT TTTCCTGTTG 2460
CCAAGAAAAA ACTGGGGTCC TGAGAGTTTT TCTTTTCCTT TCACAACAGG AAGAAACAAA 2520
CTACAGAGCC CCTAGGTATA CTGGGGCCAC CTGGGGTCTT GTTAAAAATG TGCATTTGGG 2580
GGAGGGGCGG AGAGTCTGCG TTCCCCCCAT GCAGTGCCCA GGCTGCTGCT CTGTAGGCCA 2640
CACTTTGAAT ACTGAGAGTA CCAGAGAGGA CTTGGTGGTA GGGGGTGGTG GGTGGATTCT 2700
GGTACAGTTG GAGGGAGGAG GCTTCCTGGG GTGAGGGCAC TGAGATGGGT CCTGGTGGTA 2760
AGATTGTGTG GGGAGGAGAA TAAAGGTACC CCAGATCAAC CTTGTGGGGC AACAAGTGAC 2820
CTGACAAACT CCCATCATGT ATGGCCACTG TCCCCCATTC AAGGCCAGGG ACCGTTGGAG 2880
GAGTTGGAAA GTTAAGAGCT TGAAAACTGG ATTCTGCCTC ACTGGGAGGT TCACTGACAT 2940
TTAGTCTTCT CTGAAAGATG 2960
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