EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS175-11858 
Organism
Homo sapiens 
Tissue/cell
SK-N-MC 
Coordinate
chr17:74263590-74266180 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HES2MA0616.2chr17:74263873-74263883GGCACGTGCC+6.02
HES2MA0616.2chr17:74263873-74263883GGCACGTGCC-6.02
Stat6MA0520.1chr17:74264281-74264296GTTTTCTTGAGAACT+6.37
ZNF263MA0528.1chr17:74264587-74264608AGTGGAGGGAGGAGGGGAAAG+6.37
ZNF740MA0753.2chr17:74264567-74264580GTGGGGGGGGGGC-6.29
ZNF740MA0753.2chr17:74264569-74264582GGGGGGGGGGCAG-6.33
ZfxMA0146.2chr17:74265059-74265073CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_10428chr17:74261317-74270738CD19_Primary
SE_11415chr17:74257434-74273567CD20
SE_15056chr17:74260072-74266530CD4_Memory_Primary_7pool
SE_18937chr17:74257700-74266466CD4p_CD25-_Il17-_PMAstim_Th
SE_19565chr17:74259973-74266464CD4p_CD25-_Il17p_PMAstim_Th17
SE_21340chr17:74259878-74266365CD8_Memory_7pool
SE_23599chr17:74263966-74264926Colon_Crypt_1
SE_23599chr17:74265049-74265989Colon_Crypt_1
SE_24131chr17:74264098-74264827Colon_Crypt_2
SE_24131chr17:74265148-74265617Colon_Crypt_2
SE_24931chr17:74263978-74264813Colon_Crypt_3
SE_24931chr17:74265637-74266014Colon_Crypt_3
SE_27367chr17:74258519-74266081Esophagus
SE_28090chr17:74257585-74269455Fetal_Intestine
SE_29152chr17:74254176-74269372Fetal_Intestine_Large
SE_31864chr17:74261126-74264947Gastric
SE_31864chr17:74264958-74270935Gastric
SE_32663chr17:74261503-74269696GM12878
SE_43246chr17:74259692-74266315Lung
SE_47749chr17:74264544-74264846Pancreas
SE_48284chr17:74258480-74271528Psoas_Muscle
SE_50371chr17:74254262-74264931Sigmoid_Colon
SE_50371chr17:74264998-74266657Sigmoid_Colon
SE_52552chr17:74254274-74270056Small_Intestine
SE_53757chr17:74260072-74269790Spleen
SE_55588chr17:74263663-74264593Thymus
SE_55588chr17:74265042-74265707Thymus
SE_58966chr17:74257592-74273389Ly3
SE_60322chr17:74239092-74270751Ly4
SE_60510chr17:74247565-74275632DHL6
SE_61026chr17:74257641-74276199HBL1
SE_62440chr17:74241844-74272934Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr177426401674264975
chr177426400074264899
Enhancer Sequence
TTCTAATTTT ATTTTTGAGA AAGGCCAGGG CAGGGGGAGT CTCTATGTGG CCCAAGCTGG 60
TCTTGAACTC CTGGCCTCAA GCTATCCTTC CGCCTCAGCC TCCCGAAGTG CTGGGATTAT 120
AGGTGTGAGC CACTGCACCC AGCTGGCAAT TTCTTTTCTT TTTTTTTTTT TTTGAGACAG 180
AGTTTCACTC TTATTGCCTA GGCGGAGTGC AATGGTGTGA TCTCGGCTCA CCGCAACCTT 240
CACCTCCTGG GTTCAAACGA TTCTCCTGCC TCATGGGATT ACAGGCACGT GCCACCTGTA 300
ATCCCACACC TGGCTAATTT TGTATTTTTA GTAGAGACGG GGTTTCTCCA TGTTGATCAG 360
GCTGGTCTCG AACTCCCAAC CTCAGGTGGT CCGCCTGCCT CGGCCTCCCA AAGTTCAGGG 420
ATTACAGGCG TGAGCCACTG CACCCGGCCT GGCAATTTAT TTTGGACAAA GTAAGTCAAA 480
GGAAAAAGAT CAAAAAACGA AACACTAGAG ACCAGTAACA GCAAAATGGC AAAACCAGAA 540
GTCATGAGTA ACTGATAAAT GGTTGTCCCG TACATTACTG TAGATTCCCA TAGTTGGAAG 600
CTTCCCAGTT GATAAGGAGG GCTTCCCAGT TGGAAGTGGA GAAAGGCACT ACAGACTTGA 660
AGTGGGAGGA CAAAGGTACA GGGGACAATG GGTTTTCTTG AGAACTGGCC GAGAGGGCAT 720
ATCTGGTTCA AAACCCTCAT TTTACAAAAG CAGAGAGAAG CTCCAGAGAG GTTCAGGAAC 780
TTGCCCAAGC TTACACAGGC AGGCCACCAC AGGCCTGCCA GCCATCATCC CTGCTGTTCT 840
CTGGCGGCTG TTTGAGGAGA CAGGCCTCGC TGGCTGGCGG GGAACTGGGG AAGTCGGTCA 900
CGATGCTGTG ATGCAATTGG CCTCCACCCC CACCCTTCAT TCATTGTTTC CTGCTGCCGA 960
GAAGTCATCC CCAGAGGGTG GGGGGGGGGC AGGGAGTAGT GGAGGGAGGA GGGGAAAGGT 1020
CTGGGTGGGG CCAGGCCTCT GCATTGGGTC CTTTGGCCTC CCCCTGAGGA CCCCTAGAAA 1080
GGCAAGGGTC AGAGCTCCCT TGGTGCCCTG GGTGCTGACA TGGTGTGGGG CTCAATGGAC 1140
AGGGTGTGCT AGTGTCCCCA TTCCATGTAT GTTACACACC CCCTACACAA CCTCCGGTTT 1200
CTAGCTGTGA AAGCTCCCTC TGTTTTTTTT TTTTTTTTTT TTGAGACGGA GTTTTGCTCT 1260
GCCACCTAGG CTGGAGTGCA GTGACGTGAT CTCAGCTCAC TACAACCTCC ACCTCCCGGG 1320
TTCAAGTGAT TCTCCGGCCT CAACCTCCCA AGTAGCTGGG ATTATAGACG CCCATCACCA 1380
CACCCAGCTA ATTTTTGTAT TTTTTAATAG AGACAGGGTT TCACCATGTT GGTCAGGCTG 1440
GTCTCGAACT CCTAACCTCA GGTGATCCAC CCGCCTCGGC CTCCCAAAGT GCTGGGATTA 1500
CAGACGTGAG CCACTGCGCC CTGCCAAAGC TCCCTCTTTC AAGGTGAAGA GCCCTCAAGT 1560
CGTTCCCCCA ACTCCTGCGC CTGGGGGAGG GGCCAGTGTT GCTAAAATTA GGAGAAATTC 1620
AAAGAAGGAC TCCTGTGGCT TCCTGGGAAA GGGAGAAAGC AGCTTTGAGG TCCCAGCCAG 1680
TTTTGTGTGG TCTTGTTCTC TGTGTTGCCT CTTGCCCATG CTGCTGACGA GGTGCTCCTG 1740
GATGGCACTC CAGCCCCTGC CCCCAGGGTA GTGACAGAAG ACAGCAGATG GGGGACTGTA 1800
GCTACCCCCA GGAAGAGGAC TGAGGGGCTG GACAGACTGA GAAACTGCCA GCCTGCAGGC 1860
AAGGGCAGGC CAGCTGTGTT TGTGGCCTGA GGCTACAGAC ACAGGACATT GAAATCCCTG 1920
GTTTGTGTCC TCAAGGGGCC CAGATATAAA GGGGCTCTTG ACTCTGTGCA GCGTGGCCCA 1980
GTAGATGTTA AGAGCTTGGG CCTGCAGACT TGGGAGCTGG GGAGGTCCGT CTTCTCAACT 2040
TGCCCTCTGC TGTGGGTGCA TTTTCGGGCA AGTGACTTGA CTTCTGGGCC TCAGTTTCCT 2100
CATTTGTCAT AAAGAGAGGA TAATTGAAGC CACTAAGTGT CATTGTTAAG GGAGGCAAAG 2160
CCTTCAAGGC CTGGTGGCTG TCACCCTTAG TGTGGTGTGA ACCCATCCAC CAAGGTGGCT 2220
TAACTTTTCC AGGGTTGGCA CAGGAGGGAG AGCCTCCCCG CTGGCCGCTC TCCCTTGCCT 2280
AGCAGCCTGG GAGCATCTGA GGGTGGCTGG TGGGGCAGTC AGCTGGTCTC CCTGCCCAGG 2340
GAAGGTGCGG AACAGTGGTG TCCTGGGCTG CCCCCTTGCC CTTTCACTTT AATCTGACAC 2400
CTTAGCTCCT GGGTGCAATT AACCATTTAC TTTGAATGCT CCTCGGGGTG TCATTTCCAG 2460
GCCTCATGAA ACCCCGTTGG TTTTGATAAG GTTCTTGGGT TTTGTCCTTG TTTTCTGTTT 2520
GTATTGCCTC GGGGAGAGGG CACTTTTGTC CTGTGGAAGC TGCTTGTGCG AAAATGAATG 2580
AAGCTGAAAA 2590