| Tag | Content |
|---|
EnhancerAtlas ID | HS134-54170 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr6:159273310-159276310 |
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 | GTATGCCAGC TACTATTCTT AGCTCCTTAC ATGAACTAAT CCTTTTAATC CTCACAACTA 60
CACTATGAAG CGGATGCTAC TATTGTCCAC TTTATGGGGG AAGAAACTGA GGCACAGAGA 120
GGTTAGCTTG CCTCGGGACT CTGTCTCTGC TGAGATTGGA AGCAGAAGAC TAGTTCCAGA 180
ATTCACACTC CTAACCCTAC TACAACACCT GCTCTCAAAC AGAGAAGGGA AAGGAAGTCC 240
TGGCGTTTGC ACTCTCCTTG ATCTTGTGCT GGTCTGGTCT GGACATGGAC CAAGGCTTGG 300
GGGCCTTGCA CACGTAAGTG AGTGCAGATG CCCGGCCCAG CCCCAGGGCT CCCTTGTCCT 360
TGAGCTGGGG CCACGCTGAG GCTGAGGCTG GCCTCCATGG CTTGACTTGA GGCCACCTCC 420
AGATCCACAC CCTGAAAGCT TGGGACTGGC CTTCTCAGAG AATGGGGCAA AACACTCTGA 480
CGCCAACTAC AACCATCACA AGGAGGTACA TTCTCTGTAA GGGCAAGCCT GGGGCTGCAC 540
CCAAGTAGAC TAGCAGACAC TCATTACAGA GAGAATGTTC TGGCACTCTG GCCCTGCCAA 600
AGGCTACCAG AACACAGAAG GCCCTTTCTT CCAAGGGGCC GAAGGAGGAG CAGGCACACA 660
CCATATGCCT CACTCACCAC ACGAAACCAC ACACCACATA GCACACACGC GTGCACCCTC 720
ATACCACACT GACCCTTCAC CACACACACA CCCATACACC TTCATGTCAC ACATACCACA 780
CACACAGATA TACCACATGC ACCCCATACA CCCCACCACA CACATACAAA CACCACACCA 840
TATACACACA CACACAGTAC AACATACACA CTCACACACC ATATGCCACA CACATATACT 900
TTACACATAT ACATACCTCC AAACACACAC CATGCACACA CACGGTACAC CATACACACA 960
CCACACACTA TGCACACACC ATGTACCACA CACATACCCC TCCAACATCA CATGAACACT 1020
ACGCACCCTC CCCCATACCA CACACATACA CGCACACGTA CCATGCACGC ACACACACCA 1080
CAATGTGCTG TTACTTAACA GGTTTGCCTT CCCACAACTC TATCAGCAAA CCCTTCTGGA 1140
GGCGCAGCCC ACACCTGCAT TCCAAAGAAC GCAAATCCCT TCCCTGCCCG ATGAAAGGCC 1200
CCTCCCACAG TGAGTCACAG AAACTGCAGC CGAGCAGGCA GTGGTGGGCC CCACCCTTCT 1260
CACAGGAAGT GAGAAAGAGT AAATATGTAG TTTTTCTTTG AGGGCCAATG CACATGTTAA 1320
ATGGGTGATT AAGAAGACAG AGAGCTGCTT AAAAGGTCAT GGGAGAAGTA CAATGTCTGG 1380
GGACTTGGCA GTAGCCTGGC AGAGACCGCA GGAATCCTAT AGAGTCTTTT ATGGACAGGG 1440
CTCTGAAATT CCAGAGCCTG CAGGAGGTAC CTTCCCCTTT GACTCGGCGG GGCTGTACCA 1500
CTAAGAATGC ACTGAGCATT GGGTGCACTT GGGATACCTG AGCTGTGGGG CCAGAGAGGC 1560
AGCCCTAGGG GAGAATTCCG GAGTTGGGGC TGGGTTCTTT CAGCATAAAA AATCAAAGTG 1620
TCGCTTCTTT AATGAACCTC CCGGCAAGGT CTTCCCTGAA GACCTTGAAC AAGTGTTCTT 1680
AAACAAGTGT TCCTTTATGC AATTAAAGGC CAGGGAAGCT GGGGTCTGAG AGGCCATGGA 1740
GCCATTGGGA TAATAGTGAC AGTTCGGCTA CCATTCAACT GGGCTTCTGA TGAATCATGC 1800
TGGGGGCAAG GACTCCAAAT CACCAGCTCT ACTCTATACT CGAATCAGTA GGCAGTTCAG 1860
ACAGTCTTGG GGGATTTGGG CAAACGAACG CTCCACTTAG AATCTCTCCA GAAAGACAAA 1920
GGGGGTGCCT AACAAACAAT TCAAGGACTG TGGGAAACCA ATGATCATCA AGGGCTCAGT 1980
TGTACAGTGT AAACCAAAAA GTATCTGAGA CAGGTCTCAA TCAACTGAGA AGTTTATTTT 2040
GCCAAGGTTA AGGACAGGCC AGGGAGGAAG AAACACGGAA TCACAGAAAC AGTCTATGGT 2100
CTGTGTCGTT CTTCCAAGAT GATGTTGAGG GCCTCGATGT TTAAAAGGGA AAAGTGGGCT 2160
GGAGAGGAAA GAGGAAGGGC ATGGGAATCT ACTTGTTGCA AGGGAAAAGG AGCAGGAAGA 2220
GGAACAATCA GTTACGTTTC CTCTAGCAGT CTGTAAATTG GTGCTTTACA TAAGATGAGC 2280
ATAGAGTTTA GCTGCCTGTG GTGGGGATAT CTAGCCTTTT ATCTGTAGCT ATCTGCTTAG 2340
GCACAAACAG AAAGGCAGCT TCTTGCATGA CTCAGCTTCT AGTTTAATTT TTTCCTGTTG 2400
CCAAGAAAAA ACTGGGGTCC TGAGAGTTTT TCTTTTCCTT TCACAACAGG AAGAAACAAA 2460
CTACAGAGCC CCTAGGTATA CTGGGGCCAC CTGGGGTCTT GTTAAAAATG TGCATTTGGG 2520
GGAGGGGCGG AGAGTCTGCG TTCCCCCCAT GCAGTGCCCA GGCTGCTGCT CTGTAGGCCA 2580
CACTTTGAAT ACTGAGAGTA CCAGAGAGGA CTTGGTGGTA GGGGGTGGTG GGTGGATTCT 2640
GGTACAGTTG GAGGGAGGAG GCTTCCTGGG GTGAGGGCAC TGAGATGGGT CCTGGTGGTA 2700
AGATTGTGTG GGGAGGAGAA TAAAGGTACC CCAGATCAAC CTTGTGGGGC AACAAGTGAC 2760
CTGACAAACT CCCATCATGT ATGGCCACTG TCCCCCATTC AAGGCCAGGG ACCGTTGGAG 2820
GAGTTGGAAA GTTAAGAGCT TGAAAACTGG ATTCTGCCTC ACTGGGAGGT TCACTGACAT 2880
TTAGTCTTCT CTGAAAGATG GGCATAGTTA TACCAATCCT ACAGGAGTAG TGTGAAGATT 2940
AAATGAGATG ACATATAAAG TGCTTAGGGC CTGGGGCAGC ATAAGTGGTA GAATATTTGT 3000
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