| Tag | Content |
|---|
EnhancerAtlas ID | HS176-36912 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr7:43697950-43700840 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arid5a | MA0602.1 | chr7:43698862-43698876 | TTTATCAATATTAT | - | 6.24 | | EWSR1-FLI1 | MA0149.1 | chr7:43699953-43699971 | CCTTCCTGCATTCCCTAC | - | 6.01 | | MNX1 | MA0707.1 | chr7:43699484-43699494 | GGTAATTAAA | + | 6.02 | | PHOX2A | MA0713.1 | chr7:43699486-43699497 | TAATTAAATTA | - | 6.62 | | PROP1 | MA0715.1 | chr7:43699486-43699497 | TAATTAAATTA | + | 6.32 | | PROP1 | MA0715.1 | chr7:43699486-43699497 | TAATTAAATTA | - | 6.62 | | Phox2b | MA0681.1 | chr7:43699486-43699497 | TAATTAAATTA | - | 6.62 | | Stat6 | MA0520.1 | chr7:43698647-43698662 | ATTTCTCTAGAAAGG | - | 6.08 |
|
| | Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
| SE_02027 | chr7:43698271-43698892 | Aorta | | SE_02442 | chr7:43697917-43700241 | Astrocytes | | SE_10894 | chr7:43696640-43701297 | CD20 | | SE_17400 | chr7:43697922-43699994 | CD4p_CD25-_CD45RAp_Naive | | SE_18336 | chr7:43697532-43700544 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_20054 | chr7:43697991-43701059 | CD56 | | SE_22324 | chr7:43697831-43700978 | CD8_primiary | | SE_36820 | chr7:43698205-43699883 | HMEC | | SE_37916 | chr7:43697753-43700437 | HSMMtube | | SE_39165 | chr7:43698203-43699184 | IMR90 | | SE_45276 | chr7:43698081-43699821 | NHLF | | SE_45666 | chr7:43697708-43700417 | Osteoblasts | | SE_52062 | chr7:43698091-43699846 | Skeletal_Muscle_Myoblast | | SE_54117 | chr7:43698191-43698878 | Spleen | | SE_56082 | chr7:43697844-43700651 | u87 | | SE_58298 | chr7:43621281-43741410 | Ly1 | | SE_60110 | chr7:43684678-43720092 | Ly4 | | SE_60505 | chr7:43681883-43741098 | DHL6 | | SE_62288 | chr7:43651338-43740420 | Tonsil | | SE_63857 | chr7:43698074-43699965 | HSMM | | SE_67943 | chr7:43697844-43700651 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr7 | 43700221 | 43700669 | | chr7 | 43698200 | 43700000 | | chr7 | 43698290 | 43699417 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I043657 | chr7 | 43697376 | 43700748 |
|
Enhancer Sequence | GTCTCAAAAA AAAAAAATTT ACCACTGAAA AGAAATTAGC TCAAAGATGT GATAAAATGT 60
CATCTGAGAA CAAATCAAAC CTCTCGAAAC TAAGATATAA CATAAACACC TGATAAAACA 120
TATGCTAATA TTCATAATGA ATTATAAAAC CCAAATAATG AATGAAATCG AATTGTTTTC 180
TAAACTGTAC TTTCTTAAGA CCAAATAACA TAGTAAGGGT TGTTCTCCCT CTAAAATCTA 240
CTCTAATTTC ACTCCTACCT CTCGCCAGTG TTCACTATCA AAACCTTGAA ATATTCAAGT 300
GGGAAATGCC ATGTGAAGAC TCTCTCAAAA ATAAGCAAAC AAATAAATAT CATGACATAC 360
TAGAATATGA AAGGGGGAAG CGCAATTTTA ATGTGGCAGT GAAGAACGGC ACCTCTGCCA 420
AGGTGACATG TGAGACTGGA GGGATCATTT GAAAACCAGG GGAAGGGCAC GCCAAACACG 480
CCAAGGCCCT GAGGCAGCCA CAGGCTCGGT ATCTTCAAGA AGCAGAAGGC AGGCTCGTGA 540
ATGAGGTGTG GAAGAGGAGG CCAGGCAAGA GGGCAGGGTC TTCATCATGC AGGTTTTGTA 600
GGTATGGTAG GGAGTCTGGA TTTTACTCAA AGTGTAAGAG AAGATGCTGA AGGTTTCAAT 660
CAGGAAATGA CACAGTATGA CTTGCTTTTT GTTAAAGATT TCTCTAGAAA GGACAAGAAT 720
GGAAGCAGGG AGTCCAATTA AAAGGCTCCA TGGCAGAGCT GGTGGTGGCT TGGACTAGCT 780
GGTAGCAGCA GACCTGCAAA GAAGTAAATC CACTTGAGAT ATGAAGCAGA ATTAACAGGA 840
CTTGTTGACA AATTATTAAC AGAAATTGGG GAAAGGGTGA AGGACAAGGC GCATAGCAGA 900
GTGATTTCTG AATTTATCAA TATTATCCTT AAACCTCCTT ACAAAAAACT TGAGCATTGA 960
AAACTACCAT GCAGTTGGAA CTTAGTAATG ATAAAGAGTC TTGATGGAAA GTTTTAAATA 1020
GAAAACCATG ATTTCTAAAT CATTAGTCAT GACATCTGCT TGAACAAATA CATTTCAAGG 1080
CCATTCTCTT GTAGATTTTA AACCACAGCA AGAAGGTATT CAGTACTTTC TGGCATAAAA 1140
ACTTCATGGA ATGGACTCTG ATTCATAACC ATTTTGCAAA TGAATATGAG TAGGGCAAAC 1200
CCTATTAAAC ATTTACTTCA GCATTCCTAT TAAGAGCCTC CATTTTAGAA AAAAACATTT 1260
ATAAAAATAA AACAATTTGG TATCAGTGAC TACAAAAGGA ATCTGGGAGG TTTGCTATTG 1320
ACTCTTCCCT CCCTAGAGTC CTCCCTTTAT TCTCACAGAC TCAGGTGTTT GCTTTCTATT 1380
TCTCTGGAGA GTCCTCTCCA CTCCCCTGCC TGTTTTACAT AGCCCCCCAT TCTATATTAG 1440
GGGCTGAATT GTGTCCTCCC AAAATTCATA TGTTGAAGCC CTAATTCCCA GGTCCTCAGA 1500
ACATCACAGT ATCTGGAAAA AAGGTCTTTA AAGAGGTAAT TAAATTAATA TGAGATTTTC 1560
AGGGTGCATC TTAATCCGAT AAGAAATCTG GACTCAGACA TACACACATA CAGAGAAAAG 1620
ACTGTGTTAA GACAAAAGGA GAGGGTGGCA TCTACAAGCC AAGGCAAAAG GCCTCAGAGG 1680
AAACCAACCC TGACAACACC TTCATCTTCA ACTTCTACCT CCAGACCTGT GAGAAAATAT 1740
ATTCCTGTCA TTTAAACCAC CCAGTCTGTG CTATTTTGTT AATGACGGAC CTAGCAAATT 1800
GATACACTCT ATATACCCTT TCCTACTCCC CGACCCCAAG AACATCTCAT TCAAGGGCAT 1860
GAATCTAGGT CTACTAAAAT AATCCCCACA TCTCTATCTC CAGGCCAGGT GTCCCTTCTG 1920
CACTTGAAAT TCCTAGTAAA TACTTCCACA AGTCCCCATG TGAGCTCCTG CCCTGACCCT 1980
CCTCCACTCC ACACCAGGTC TCCCCTTCCT GCATTCCCTA CTTGGTGAAC GGAACCAACC 2040
CAGGTGCCTA AATCAGATAC CTGGGAGTCA TCCTCATAAA AACAAAAGTG GCTTCCATAT 2100
GTTTACTCAC ATGCAAGAAA GAGCTTTGCA TGTATCTTAT CAAATCTTCT TAAGGGTCTT 2160
ATAAAGCAGG AATTACTCTC CCTATTTTGT AAGTGAAGAA GCTGAGATTT GGGTTAATTG 2220
TGAGAGCCAC TCCTTTAAGA AGTGACAGAG TCAGGATTTG AGCCCAGGTC TGCCTGACTC 2280
CAGGGCCTAT GCTCCTCACC TAAATTACCC CCAATCTAAT CAGGCCCCCT CAAACCCATA 2340
CAATCTGTTT CCTAAATATC TTTGGATATT TTCCACCTTG TCTTTATCCT CCAAATGCCC 2400
TAATTTGGCC CCTAAGTATC TCTTTCAACC AAGGGGTTAT CAAGACTGCT CTGCCTTTGG 2460
CCTCATTCCT CTCTAGTCTA GAATCCTTCT AATACAGAAA ACTGATTGTA TCCCATTCTT 2520
CAATGGCTCC CCATCCTATT CAGAATAAAA TCTAAGCTTC TTTGCATTAC ACGGTCTTAC 2580
TGCCCAGTTT CCTCACCACA TTCTTAAATC CCAACCACCC TCCTGAGTTA CACTGAGCAG 2640
AACATGGTAA GTGCCACAGG CCCTGGCACT TCCTGTCCAC CCTGGCAACC CTAACCACCC 2700
TTTAAGTCTC AGCTCAAATG CTAATTTTAG TGTTAGAAGA GGTCCTTGGC TTACCAAGGC 2760
AAACTTAATT TTCTTTCACC TATACTTTCA CAATAGTTAC TTTAGTATGC TATGGCTGTT 2820
AAATTACCTA ATTCTCAATA GACATTTAAC TACTTTAAGG CTAGGATTGG GTTTTCCATT 2880
TTAGAATGCC 2890
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