| Tag | Content |
|---|
EnhancerAtlas ID | HS175-27911 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr6:159273600-159276280 |
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 |
|
| | 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 | CAAGGCTTGG GGGCCTTGCA CACGTAAGTG AGTGCAGATG CCCGGCCCAG CCCCAGGGCT 60
CCCTTGTCCT TGAGCTGGGG CCACGCTGAG GCTGAGGCTG GCCTCCATGG CTTGACTTGA 120
GGCCACCTCC AGATCCACAC CCTGAAAGCT TGGGACTGGC CTTCTCAGAG AATGGGGCAA 180
AACACTCTGA CGCCAACTAC AACCATCACA AGGAGGTACA TTCTCTGTAA GGGCAAGCCT 240
GGGGCTGCAC CCAAGTAGAC TAGCAGACAC TCATTACAGA GAGAATGTTC TGGCACTCTG 300
GCCCTGCCAA AGGCTACCAG AACACAGAAG GCCCTTTCTT CCAAGGGGCC GAAGGAGGAG 360
CAGGCACACA CCATATGCCT CACTCACCAC ACGAAACCAC ACACCACATA GCACACACGC 420
GTGCACCCTC ATACCACACT GACCCTTCAC CACACACACA CCCATACACC TTCATGTCAC 480
ACATACCACA CACACAGATA TACCACATGC ACCCCATACA CCCCACCACA CACATACAAA 540
CACCACACCA TATACACACA CACACAGTAC AACATACACA CTCACACACC ATATGCCACA 600
CACATATACT TTACACATAT ACATACCTCC AAACACACAC CATGCACACA CACGGTACAC 660
CATACACACA CCACACACTA TGCACACACC ATGTACCACA CACATACCCC TCCAACATCA 720
CATGAACACT ACGCACCCTC CCCCATACCA CACACATACA CGCACACGTA CCATGCACGC 780
ACACACACCA CAATGTGCTG TTACTTAACA GGTTTGCCTT CCCACAACTC TATCAGCAAA 840
CCCTTCTGGA GGCGCAGCCC ACACCTGCAT TCCAAAGAAC GCAAATCCCT TCCCTGCCCG 900
ATGAAAGGCC CCTCCCACAG TGAGTCACAG AAACTGCAGC CGAGCAGGCA GTGGTGGGCC 960
CCACCCTTCT CACAGGAAGT GAGAAAGAGT AAATATGTAG TTTTTCTTTG AGGGCCAATG 1020
CACATGTTAA ATGGGTGATT AAGAAGACAG AGAGCTGCTT AAAAGGTCAT GGGAGAAGTA 1080
CAATGTCTGG GGACTTGGCA GTAGCCTGGC AGAGACCGCA GGAATCCTAT AGAGTCTTTT 1140
ATGGACAGGG CTCTGAAATT CCAGAGCCTG CAGGAGGTAC CTTCCCCTTT GACTCGGCGG 1200
GGCTGTACCA CTAAGAATGC ACTGAGCATT GGGTGCACTT GGGATACCTG AGCTGTGGGG 1260
CCAGAGAGGC AGCCCTAGGG GAGAATTCCG GAGTTGGGGC TGGGTTCTTT CAGCATAAAA 1320
AATCAAAGTG TCGCTTCTTT AATGAACCTC CCGGCAAGGT CTTCCCTGAA GACCTTGAAC 1380
AAGTGTTCTT AAACAAGTGT TCCTTTATGC AATTAAAGGC CAGGGAAGCT GGGGTCTGAG 1440
AGGCCATGGA GCCATTGGGA TAATAGTGAC AGTTCGGCTA CCATTCAACT GGGCTTCTGA 1500
TGAATCATGC TGGGGGCAAG GACTCCAAAT CACCAGCTCT ACTCTATACT CGAATCAGTA 1560
GGCAGTTCAG ACAGTCTTGG GGGATTTGGG CAAACGAACG CTCCACTTAG AATCTCTCCA 1620
GAAAGACAAA GGGGGTGCCT AACAAACAAT TCAAGGACTG TGGGAAACCA ATGATCATCA 1680
AGGGCTCAGT TGTACAGTGT AAACCAAAAA GTATCTGAGA CAGGTCTCAA TCAACTGAGA 1740
AGTTTATTTT GCCAAGGTTA AGGACAGGCC AGGGAGGAAG AAACACGGAA TCACAGAAAC 1800
AGTCTATGGT CTGTGTCGTT CTTCCAAGAT GATGTTGAGG GCCTCGATGT TTAAAAGGGA 1860
AAAGTGGGCT GGAGAGGAAA GAGGAAGGGC ATGGGAATCT ACTTGTTGCA AGGGAAAAGG 1920
AGCAGGAAGA GGAACAATCA GTTACGTTTC CTCTAGCAGT CTGTAAATTG GTGCTTTACA 1980
TAAGATGAGC ATAGAGTTTA GCTGCCTGTG GTGGGGATAT CTAGCCTTTT ATCTGTAGCT 2040
ATCTGCTTAG GCACAAACAG AAAGGCAGCT TCTTGCATGA CTCAGCTTCT AGTTTAATTT 2100
TTTCCTGTTG CCAAGAAAAA ACTGGGGTCC TGAGAGTTTT TCTTTTCCTT TCACAACAGG 2160
AAGAAACAAA CTACAGAGCC CCTAGGTATA CTGGGGCCAC CTGGGGTCTT GTTAAAAATG 2220
TGCATTTGGG GGAGGGGCGG AGAGTCTGCG TTCCCCCCAT GCAGTGCCCA GGCTGCTGCT 2280
CTGTAGGCCA CACTTTGAAT ACTGAGAGTA CCAGAGAGGA CTTGGTGGTA GGGGGTGGTG 2340
GGTGGATTCT GGTACAGTTG GAGGGAGGAG GCTTCCTGGG GTGAGGGCAC TGAGATGGGT 2400
CCTGGTGGTA AGATTGTGTG GGGAGGAGAA TAAAGGTACC CCAGATCAAC CTTGTGGGGC 2460
AACAAGTGAC CTGACAAACT CCCATCATGT ATGGCCACTG TCCCCCATTC AAGGCCAGGG 2520
ACCGTTGGAG GAGTTGGAAA GTTAAGAGCT TGAAAACTGG ATTCTGCCTC ACTGGGAGGT 2580
TCACTGACAT TTAGTCTTCT CTGAAAGATG GGCATAGTTA TACCAATCCT ACAGGAGTAG 2640
TGTGAAGATT AAATGAGATG ACATATAAAG TGCTTAGGGC 2680
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