| Tag | Content |
|---|
EnhancerAtlas ID | HS191-34060 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr6:159273350-159276240 |
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 | CCTTTTAATC CTCACAACTA CACTATGAAG CGGATGCTAC TATTGTCCAC TTTATGGGGG 60
AAGAAACTGA GGCACAGAGA GGTTAGCTTG CCTCGGGACT CTGTCTCTGC TGAGATTGGA 120
AGCAGAAGAC TAGTTCCAGA ATTCACACTC CTAACCCTAC TACAACACCT GCTCTCAAAC 180
AGAGAAGGGA AAGGAAGTCC TGGCGTTTGC ACTCTCCTTG ATCTTGTGCT GGTCTGGTCT 240
GGACATGGAC CAAGGCTTGG GGGCCTTGCA CACGTAAGTG AGTGCAGATG CCCGGCCCAG 300
CCCCAGGGCT CCCTTGTCCT TGAGCTGGGG CCACGCTGAG GCTGAGGCTG GCCTCCATGG 360
CTTGACTTGA GGCCACCTCC AGATCCACAC CCTGAAAGCT TGGGACTGGC CTTCTCAGAG 420
AATGGGGCAA AACACTCTGA CGCCAACTAC AACCATCACA AGGAGGTACA TTCTCTGTAA 480
GGGCAAGCCT GGGGCTGCAC CCAAGTAGAC TAGCAGACAC TCATTACAGA GAGAATGTTC 540
TGGCACTCTG GCCCTGCCAA AGGCTACCAG AACACAGAAG GCCCTTTCTT CCAAGGGGCC 600
GAAGGAGGAG CAGGCACACA CCATATGCCT CACTCACCAC ACGAAACCAC ACACCACATA 660
GCACACACGC GTGCACCCTC ATACCACACT GACCCTTCAC CACACACACA CCCATACACC 720
TTCATGTCAC ACATACCACA CACACAGATA TACCACATGC ACCCCATACA CCCCACCACA 780
CACATACAAA CACCACACCA TATACACACA CACACAGTAC AACATACACA CTCACACACC 840
ATATGCCACA CACATATACT TTACACATAT ACATACCTCC AAACACACAC CATGCACACA 900
CACGGTACAC CATACACACA CCACACACTA TGCACACACC ATGTACCACA CACATACCCC 960
TCCAACATCA CATGAACACT ACGCACCCTC CCCCATACCA CACACATACA CGCACACGTA 1020
CCATGCACGC ACACACACCA CAATGTGCTG TTACTTAACA GGTTTGCCTT CCCACAACTC 1080
TATCAGCAAA CCCTTCTGGA GGCGCAGCCC ACACCTGCAT TCCAAAGAAC GCAAATCCCT 1140
TCCCTGCCCG ATGAAAGGCC CCTCCCACAG TGAGTCACAG AAACTGCAGC CGAGCAGGCA 1200
GTGGTGGGCC CCACCCTTCT CACAGGAAGT GAGAAAGAGT AAATATGTAG TTTTTCTTTG 1260
AGGGCCAATG CACATGTTAA ATGGGTGATT AAGAAGACAG AGAGCTGCTT AAAAGGTCAT 1320
GGGAGAAGTA CAATGTCTGG GGACTTGGCA GTAGCCTGGC AGAGACCGCA GGAATCCTAT 1380
AGAGTCTTTT ATGGACAGGG CTCTGAAATT CCAGAGCCTG CAGGAGGTAC CTTCCCCTTT 1440
GACTCGGCGG GGCTGTACCA CTAAGAATGC ACTGAGCATT GGGTGCACTT GGGATACCTG 1500
AGCTGTGGGG CCAGAGAGGC AGCCCTAGGG GAGAATTCCG GAGTTGGGGC TGGGTTCTTT 1560
CAGCATAAAA AATCAAAGTG TCGCTTCTTT AATGAACCTC CCGGCAAGGT CTTCCCTGAA 1620
GACCTTGAAC AAGTGTTCTT AAACAAGTGT TCCTTTATGC AATTAAAGGC CAGGGAAGCT 1680
GGGGTCTGAG AGGCCATGGA GCCATTGGGA TAATAGTGAC AGTTCGGCTA CCATTCAACT 1740
GGGCTTCTGA TGAATCATGC TGGGGGCAAG GACTCCAAAT CACCAGCTCT ACTCTATACT 1800
CGAATCAGTA GGCAGTTCAG ACAGTCTTGG GGGATTTGGG CAAACGAACG CTCCACTTAG 1860
AATCTCTCCA GAAAGACAAA GGGGGTGCCT AACAAACAAT TCAAGGACTG TGGGAAACCA 1920
ATGATCATCA AGGGCTCAGT TGTACAGTGT AAACCAAAAA GTATCTGAGA CAGGTCTCAA 1980
TCAACTGAGA AGTTTATTTT GCCAAGGTTA AGGACAGGCC AGGGAGGAAG AAACACGGAA 2040
TCACAGAAAC AGTCTATGGT CTGTGTCGTT CTTCCAAGAT GATGTTGAGG GCCTCGATGT 2100
TTAAAAGGGA AAAGTGGGCT GGAGAGGAAA GAGGAAGGGC ATGGGAATCT ACTTGTTGCA 2160
AGGGAAAAGG AGCAGGAAGA GGAACAATCA GTTACGTTTC CTCTAGCAGT CTGTAAATTG 2220
GTGCTTTACA TAAGATGAGC ATAGAGTTTA GCTGCCTGTG GTGGGGATAT CTAGCCTTTT 2280
ATCTGTAGCT ATCTGCTTAG GCACAAACAG AAAGGCAGCT TCTTGCATGA CTCAGCTTCT 2340
AGTTTAATTT TTTCCTGTTG CCAAGAAAAA ACTGGGGTCC TGAGAGTTTT TCTTTTCCTT 2400
TCACAACAGG AAGAAACAAA CTACAGAGCC CCTAGGTATA CTGGGGCCAC CTGGGGTCTT 2460
GTTAAAAATG TGCATTTGGG GGAGGGGCGG AGAGTCTGCG TTCCCCCCAT GCAGTGCCCA 2520
GGCTGCTGCT CTGTAGGCCA CACTTTGAAT ACTGAGAGTA CCAGAGAGGA CTTGGTGGTA 2580
GGGGGTGGTG GGTGGATTCT GGTACAGTTG GAGGGAGGAG GCTTCCTGGG GTGAGGGCAC 2640
TGAGATGGGT CCTGGTGGTA AGATTGTGTG GGGAGGAGAA TAAAGGTACC CCAGATCAAC 2700
CTTGTGGGGC AACAAGTGAC CTGACAAACT CCCATCATGT ATGGCCACTG TCCCCCATTC 2760
AAGGCCAGGG ACCGTTGGAG GAGTTGGAAA GTTAAGAGCT TGAAAACTGG ATTCTGCCTC 2820
ACTGGGAGGT TCACTGACAT TTAGTCTTCT CTGAAAGATG GGCATAGTTA TACCAATCCT 2880
ACAGGAGTAG 2890
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