| Tag | Content |
|---|
EnhancerAtlas ID | HS133-02647 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:159891380-159893220 |
Target genes | | Number: 15 | Name | Ensembl ID |
|
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr1:159892832-159892845 | AGCAGCTGTTTCT | + | 6.28 | | Tcf12 | MA0521.1 | chr1:159892831-159892842 | CAGCAGCTGTT | - | 6.32 | | YY1 | MA0095.2 | chr1:159892039-159892051 | CAACATGGCTGC | + | 6.14 |
|
| | Number of super-enhancer constituents: 46 | ID | Coordinate | Tissue/cell |
| SE_02009 | chr1:159887204-159896462 | Aorta | | SE_02391 | chr1:159891163-159896016 | Astrocytes | | SE_09609 | chr1:159888811-159896163 | CD14 | | SE_10233 | chr1:159889294-159896142 | CD19_Primary | | SE_10984 | chr1:159884833-159896640 | CD20 | | SE_11910 | chr1:159890466-159896330 | CD3 | | SE_12862 | chr1:159890202-159896191 | CD34_Primary_RO01480 | | SE_13325 | chr1:159887045-159896510 | CD34_Primary_RO01536 | | SE_14052 | chr1:159890274-159896187 | CD34_Primary_RO01549 | | SE_14513 | chr1:159890132-159896515 | CD4_Memory_Primary_7pool | | SE_15769 | chr1:159891344-159896220 | CD4_Memory_Primary_8pool | | SE_15949 | chr1:159891339-159896140 | CD4_Naive_Primary_7pool | | SE_16460 | chr1:159890826-159896099 | CD4_Naive_Primary_8pool | | SE_16913 | chr1:159890317-159896307 | CD4p_CD225int_CD127p_Tmem | | SE_17500 | chr1:159889525-159896840 | CD4p_CD25-_CD45RAp_Naive | | SE_17880 | chr1:159889025-159896700 | CD4p_CD25-_CD45ROp_Memory | | SE_19597 | chr1:159888663-159896506 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20057 | chr1:159890184-159896627 | CD56 | | SE_20849 | chr1:159889345-159896337 | CD8_Memory_7pool | | SE_21561 | chr1:159891197-159896204 | CD8_Naive_7pool | | SE_22506 | chr1:159889745-159896593 | CD8_primiary | | SE_23567 | chr1:159891451-159896346 | Colon_Crypt_1 | | SE_23939 | chr1:159892115-159896031 | Colon_Crypt_2 | | SE_25013 | chr1:159890918-159896336 | Colon_Crypt_3 | | SE_30108 | chr1:159891067-159896091 | Fetal_Muscle | | SE_31985 | chr1:159891083-159896707 | Gastric | | SE_34858 | chr1:159890807-159896516 | HeLa | | SE_36438 | chr1:159891272-159896570 | HMEC | | SE_38165 | chr1:159890321-159896029 | HUVEC | | SE_40207 | chr1:159890880-159896228 | K562 | | SE_41182 | chr1:159890906-159896421 | Left_Ventricle | | SE_42315 | chr1:159887173-159896572 | Lung | | SE_44957 | chr1:159891221-159895990 | NHLF | | SE_47692 | chr1:159891560-159896059 | Pancreas | | SE_48986 | chr1:159891201-159896458 | Right_Atrium | | SE_49778 | chr1:159891574-159893172 | Right_Ventricle | | SE_50509 | chr1:159888888-159896553 | Sigmoid_Colon | | SE_52604 | chr1:159889149-159896485 | Small_Intestine | | SE_53483 | chr1:159887801-159896526 | Spleen | | SE_55434 | chr1:159890662-159896015 | Thymus | | SE_58180 | chr1:159892507-159896090 | VACO_9m | | SE_59359 | chr1:159879583-159907614 | Ly3 | | SE_63031 | chr1:159879414-159896447 | Tonsil | | SE_63399 | chr1:159883649-159916570 | NCI-H69 | | SE_64771 | chr1:159890244-159896649 | NHEK | | SE_65431 | chr1:159891110-159896368 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AAGCTTGTAG CAATTTGTTA CAGCAGAAAT AGGAAACTAA TACAGGAGCC CTGGGTGATA 60
TTTTTGGGGA AACCTGGAGA AGAGAAGGCA AGACGGGGAA ATACACAGGA GGGTTTCTTT 120
AACTTCGTTG GAGGAGCTTG ATTAGCAAGA ACTGGGTGGT TTCCCGACCA ATGGCCTGAG 180
TTGGCGGACC TCACTGTGGC AGTGTGTTCC CACCACACTC ACCACCTGGG TCTGACACTC 240
AGGGGCTGAG CAAGACCCGG GCATGGTATG GATGCCAAGG GGAGCCAAGA ACCAAGAATG 300
GGCCACAGTC CCCATTTTCT GTCCCATCCC CACCCTGGTT TGGCTTTTCT CTCTTCTCCA 360
AAACAGAGCT AGCTGTCAGG CTGCTCACGA AAGGGGACCC CCAGGACAGG CATCTGCGTT 420
CAAGGGGAAG AAAGAGAGCC ACCCCTTCTA ACCACATCTG GCTCCAGGCC AGGTTGGCCT 480
TCAGGGATGA AGTCACTCCA GCTCCCCCTC TCCCACACAC CCAGGTTAAA CAATCCCGTC 540
ACCCCCTCTC AATGGACCTT GGGGCTCTGC GAAATACAAG GGGACCAGCC TGCCTCAAAC 600
CCTCAACACC TCTCGGCCGC AGAGGCTGTG TCTTGGGCCA GTCCCTCCCG TCCCGACTCC 660
AACATGGCTG CTCCTTTTTA CCCCAGCTTA TCAAGCTGCA CATTTCCGGC AGATCCTCCC 720
CTAAATCAGT TATTTTTAAA CCTCATTAAG AGCAACCCGC CCCCTCCACT TCCCCCAGCC 780
CGAAAGCTGG GCCAGATAAA TGTCAGTCTG GGCCCCGACC CACAGCGCCA GGCACACACA 840
CCATCAGCTT GGGGAAGGCA GGCGGGGTGG GGTGGCTGAG TTCTGAGGAG AAACCAAGAG 900
AAGCATCCCT GCCCTTCCCA GAGGCCACTC CACCATAGAA ACCTCTAACC TCTGATGCAC 960
AGGGGAATGG CTGGAAGACA GGTAGGAAGA GGAAGGGGCT AAGAGCTACT ACCACCAGTA 1020
AGCCCCCTTT CCGCAGCCCA GTTCCAGACC TCTCTCCTGG GAGTGGCTGT GCTCAGGGCT 1080
GTTTCCAGGG ACCAAGTGGC CTGAGGCTCG GGGATCACCA TGGCACAGGT AAAGAAAGGG 1140
CAGGAGAATG ATTAACCTAG ACACTGGGGT TAAGAGCAGA GAGAAAGGCC TGAAGCCAGA 1200
CACTTCCAGT GCCCCCCAAC CCCCCAAGGC AGGACAAACT TGGCCTCCCA GACCCACCAC 1260
TGGGTGGAAA GTGGATGCTG AGGAACCCCC TCCACCGCCC AACGCTGGGG CCTGGACACA 1320
GCTGGCAGGG TCACGGCCTC CAGCTGCAGT GTATCTGCTC CACTCTGGGG CCATTGCCCT 1380
CAAGCTCTGA GGTGCCAGAG CCATAGGGCG GGGTCCTGAG AAGGGGCAGT TCCAACCAGG 1440
CCAGGCCTGG TCAGCAGCTG TTTCTCTTCC CCACCCCCAC GGGCAGGCAG AAGCTGATGG 1500
GCTGCGGCTG CTGGAGCTGG GAAGGCCCAC CCTAGGGACA CCCAGGGGAC CTGCCCCTGC 1560
CTTCCCTCAA ACATAAAGAA AACAGTAAGC AAGTTGCCTA CCAGGGTGAG AAGAGATATG 1620
CCCAGCTGGA AGACAGGTGT GGGGGACCCC CAGAGCTGGG GACCCCAAAG GAAGGTGACA 1680
GCTGAACAAC CTGGGGGATG GACTGGCAGG GAGCAACCTA AACCCTAGCG CTACTGCAGC 1740
TGTGAGAACA ACCCTCACCC TCACCCTGGA GTTACAATAG GCGGGAAACG GGGAGGGGCC 1800
ACGCAAGGCA CTCGGCCCCA CCCAGACCCT GGGCTGGAAG 1840
|
