| Tag | Content |
|---|
EnhancerAtlas ID | HS133-06861 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:6290800-6293570 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP1 | MA0079.4 | chr12:6291837-6291852 | AGAGGGCGTGGCCTG | - | 6.15 |
|
| | Number of super-enhancer constituents: 36 | ID | Coordinate | Tissue/cell |
| SE_00985 | chr12:6290507-6292062 | Adrenal_Gland | | SE_00985 | chr12:6292206-6292982 | Adrenal_Gland | | SE_01613 | chr12:6290594-6292119 | Aorta | | SE_01613 | chr12:6292178-6293897 | Aorta | | SE_03988 | chr12:6290792-6291792 | Brain_Anterior_Caudate | | SE_04905 | chr12:6289324-6293306 | Brain_Cingulate_Gyrus | | SE_05857 | chr12:6287388-6293430 | Brain_Hippocampus_Middle | | SE_07876 | chr12:6289745-6293464 | Brain_Inferior_Temporal_Lobe | | SE_23086 | chr12:6290753-6292057 | Colon_Crypt_1 | | SE_23086 | chr12:6292201-6293938 | Colon_Crypt_1 | | SE_23760 | chr12:6290811-6292000 | Colon_Crypt_2 | | SE_23760 | chr12:6292242-6293084 | Colon_Crypt_2 | | SE_23760 | chr12:6293275-6293833 | Colon_Crypt_2 | | SE_24754 | chr12:6291005-6292084 | Colon_Crypt_3 | | SE_24754 | chr12:6292220-6293863 | Colon_Crypt_3 | | SE_25881 | chr12:6290586-6291938 | Duodenum_Smooth_Muscle | | SE_25881 | chr12:6292265-6293935 | Duodenum_Smooth_Muscle | | SE_26531 | chr12:6290619-6292172 | Esophagus | | SE_26531 | chr12:6292175-6293815 | Esophagus | | SE_27879 | chr12:6290695-6293924 | Fetal_Intestine | | SE_28805 | chr12:6290511-6293953 | Fetal_Intestine_Large | | SE_30052 | chr12:6290681-6292144 | Fetal_Muscle | | SE_31631 | chr12:6290651-6293026 | Gastric | | SE_34881 | chr12:6288010-6291925 | HeLa | | SE_37709 | chr12:6286475-6292578 | HSMMtube | | SE_37940 | chr12:6286549-6293824 | HUVEC | | SE_41013 | chr12:6288021-6292951 | Left_Ventricle | | SE_42122 | chr12:6287877-6292200 | Lung | | SE_42122 | chr12:6292204-6293894 | Lung | | SE_48662 | chr12:6287969-6292096 | Right_Atrium | | SE_50072 | chr12:6290476-6292094 | Sigmoid_Colon | | SE_50072 | chr12:6292172-6294061 | Sigmoid_Colon | | SE_52457 | chr12:6287948-6292107 | Small_Intestine | | SE_52457 | chr12:6292166-6294018 | Small_Intestine | | SE_53862 | chr12:6287321-6293849 | Spleen | | SE_54512 | chr12:6288437-6293993 | Stomach_Smooth_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 6292247 | 6292800 | | chr12 | 6291358 | 6291755 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I006177 | chr12 | 6286985 | 6293820 |
|
Enhancer Sequence | TGGGGGTAAA AGAGGGAATA AAAGCAAAAC ATCCCATGCC CTCAAGGAAC GTCTAGTCCA 60
GGATTAGAAG TGGGGCAGTC CCAGGAAGGA GCCATCTTGA CAGTGAATTC ACGCGGAAGA 120
CGCGTGAACC CAGCTGGCCT GGAGAGACAG AGGTGCTTTG CAGGGCATGG GGAAGCCAGC 180
AGGTCCCAGT CGAGAAACCT GGTTTTCTGT CTGGGTTGGT TGAAGACTCT TTGTCCCAGA 240
AGGAGTCGCT TGTTTGCTTG TTCATCTTAA GTTTAAATTG AGAGAGGTTA ACGGCTTTTG 300
CCTCAGAAGG CAGGCTGGCC TGGCAGGGTG TGTGTTGTGA GGTGCAGAAA CACATCTTCC 360
CCAGCTGGCC TCACAGGCCA AGAAGCAGAT AATGTCTTCC TTCTGCCAGC TTCCCCGCAG 420
CTTGGTTTTC CTGGGACAGT TCCTCCGCTG GAGGAAGGGA CAGGGGATGG GGACAGGGGA 480
TGGAGGAGGA GTTGGGGAGA CCCTTCAGAG AGTGTGGCAG AAACACGTGT GTACAGGCTG 540
GCACACGAGT CACAGAGGCA ACAGGGTGGC TGCGGGGAGA AATGTGAGCA GAGCTCATGC 600
AATTGTCGTG AGTGAGTGCG CTCTCGCGGC TCTAAGGATT TGGGAAAACA ACTTGCAGAT 660
CCAGGCATGT TTACGTAGGG AGGGGTGCCG TGTGCTGGAC CAGGTCCAGA ACTAAAAATA 720
ACACAGTATT TCTGTGCCCA GCAAGAGCGC TAGCATCTGT GGGGTTTGCG TGGTGGGAAG 780
AGTGTGGTTT CAGCTGAACC AGGCGCAGTG TGACCAGAAC AGTAGGAGGG AAGGCCAGGC 840
CTGGGTGGGA GGCCCCAGGA TGGGCGGGGG AAGGACTGAG GGCGAAGGCC ATCCCAACTC 900
GCAGCAGAAA AAGCCTCCAG GCGGTCACGG GCTGCCCATC TCGTGAGGCC AGATGTGGGT 960
CCTCCTGCAT ATCTGAAACA GCACAGAGCA TTGGGGCAGC CTCCAAACCT CCCCTATAAG 1020
GAGCAGTTAA GGGATCCAGA GGGCGTGGCC TGGAGCAGAG AGAAGGGAAG CAACATGTGT 1080
GGGGCATTCA CAAGTGCAGG ATGCCTTCTC CGGGCTCCCA TGATGATCCA GACAGGTAGG 1140
CGTTTTCCTT CCCTTTTTGC AGATTGTGAA AACAGCGTTC AAAAAAGACT CATGGGCCGG 1200
GCGCGGTGGA TCACGCCTGT AATCCCAGCA CTTTGGGAGG CCAAGGCAGG CAGATCACAA 1260
GGCCAGGAGT TGAAGACCAA CCTGGCCAAC ATGATGAAAC CCTGTCTCTA CTAAAAATAC 1320
AAAAATTAGC CGGACGTGAT GGTGGGCACC TGTAATCCCA GCTACTCAGG AGGCTGAGGC 1380
AGGAGAATCG CTTGAAACCG GAAGGCAGAG GTTGCAGTGA GCCGAGATTG CGCCACTGCA 1440
CTCCAGCCTG GTCAATAAGA GTGAAACTCT GTCTCAAAAA CAAACCAACC AACAAACCAA 1500
AAACTCTTGT AACCCTGGGG CCACCCAGCC ACAAAGAGGC AGGGCTGGGA CAGGCCCCTG 1560
CAAGTCTCCT CTGGAAGGCC AAAGGGCTGC TACTAGGAAG GGGTGGCAGA CTCATCCCAT 1620
GTGGCTTCAG AGGGCAGGAC ATGGACAAAG GTTATGGGAA GGGAGGGAAA CTTTCCAATA 1680
ACCAGACTGC ACAAGAGTGG AGTGGCCTGC CTCAGGAGGG GTAAGCTCAT GCAAAAGCTG 1740
GCTGTTGGGG ACATTGGGAG GGACTCTGAA GGTCACCACC ACTCTGAATC AATGCTGTGT 1800
GGGAGGATGC CAGGGTCCAC TGGACCCATG ACGTGCCTTT AGCGTGGGAA GCAGGGAACC 1860
TCAACTTTGG AAAGAGTGAG GGCACAGTGA TGTCCAGCCA CTCCCAGAAG CCGTCTGTTA 1920
ATAGAGCAAC CCCTCGGGCG GTGTGCAATC CTAATGACCA GCCCCAGGAC ATTGGAAACA 1980
GGGTCCTGCT GACCACAGTC TAGGAGACAG GGCTGCACAC AGACGGAACC AAGCACACAA 2040
GACGAGAGAG GGTGTGTACC GCAGAAACCA AGGGCTCATT TATGTGCTGC GTTCTCAGTC 2100
TGCAAGGAGT CAGAAGAGAG GACAGTGAGG CCAGGAGAAC TCAGGGAACA CTCCTTGTTG 2160
TAATCATCAC AGTTATGTAA CTCATATTAC CAGCTGTTCT TTCGTGAGCA TTCTCTATGT 2220
GCCAGGCTAA GTGTTTTGTA TGCACTGTAT GATTTAATCC TAGAACAACA CTATGAAGCA 2280
GGAGCTCTTA GTATTCCCCT TTTACAGATG AGGAGGCAGG CTCAGAGAGG TGATGTAACT 2340
TGCCCAGAAT TATATAACTA GTGTGTGGCA GAGCCTGGAC TCAAGCCCAG ATCTGTTGGA 2400
CTCCAGACCC CGTGTAGAAC CATAAGGAAC TGATGCTGCT TCAATTTCTG CACTGATACG 2460
GAAATCTCTC CGAGATATCA TGCCGTTGTT TTCTATTGTT GCTATAGCAT ATTATCACAA 2520
GTTTAACACA TATTTATTGC ACACTTCTGG AGGTCAGCAG TCTGACATGT GGGTCTCACT 2580
GGGCTAAAAT CTCAGTGTGG GCAGGGCTGT GTTCCCCTCT GGAGGCTGCA GGGGAGAATC 2640
CCTTTCCTTG CCTTTCCCAG CTTCTAGAGG CTGCCTGCAT TCCTTGGCTC CTGGCCCCTC 2700
CTCTGTCTGC AAAGCCACCA TTGTCATGTC TCTCTAACCC TTTGTCCCAG TTCCCTCTGA 2760
CCACAGCCAG 2770
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