EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-59486 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chrX:40033480-40036260 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ArntlMA0603.1chrX:40036088-40036098GCACGTGACC-6.02
RREB1MA0073.1chrX:40034411-40034431GGGGGTGGGGTGGGGCGGGG-6.18
RREB1MA0073.1chrX:40036206-40036226CCCCACCCCACCCCCTACCT+7.21
RREB1MA0073.1chrX:40036201-40036221CCCCACCCCACCCCACCCCC+7.67
RREB1MA0073.1chrX:40034406-40034426GGGCTGGGGGTGGGGTGGGG-7.6
ZfxMA0146.2chrX:40034513-40034527CAGGCCCCGGCTGG-6.11
ZfxMA0146.2chrX:40035598-40035612CCGGCCTCGGCCTC+6.28
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_01309chrX:40032735-40036795Adrenal_Gland
SE_10489chrX:40028005-40037299CD19_Primary
SE_12441chrX:40028224-40037012CD3
SE_13187chrX:40029966-40036585CD34_Primary_RO01480
SE_13805chrX:40028268-40037234CD34_Primary_RO01536
SE_14344chrX:40029761-40037049CD34_Primary_RO01549
SE_15054chrX:40026645-40037112CD4_Memory_Primary_7pool
SE_26729chrX:40030073-40036950Esophagus
SE_31755chrX:40030098-40036960Gastric
SE_32909chrX:40033848-40036162H1
SE_34319chrX:40025113-40037081HCT-116
SE_39958chrX:40029745-40037040K562
SE_41477chrX:40032964-40037003Left_Ventricle
SE_42747chrX:40030207-40037520Lung
SE_49191chrX:40030107-40036942Right_Atrium
SE_52969chrX:40029971-40037549Small_Intestine
SE_54123chrX:40032886-40037231Spleen
SE_55438chrX:40032592-40037070Thymus
SE_56999chrX:40033538-40036784VACO_400
SE_57737chrX:40034438-40036171VACO_503
SE_59437chrX:40011613-40049393Ly3
SE_60054chrX:40006843-40037107Ly4
SE_61279chrX:40005072-40049257HBL1
SE_61737chrX:40005446-40039231Toledo
SE_62904chrX:40005186-40037678Tonsil
SE_65537chrX:40032894-40036865Pancreatic_islets
SE_66639chrX:40032989-40035974Jurkat
SE_68820chrX:40032750-40036863H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chrX4003437740034649
chrX4003469440035505
Enhancer Sequence
TCGGAACTGT GCGTGCCAAG CTGCCAGCCC CGAGAAAGAC AAAGAACACG GGCGCCTCCA 60
GGTTTGCTTC TGAGGCCTCA GGGTCACCTC TGGGGCTTCC CCTTCACAGC CTCCGGCCCC 120
TACAAGACGC TCCCAGCCAG CCTCCGGAAC AAACCCGCAG CCCTAAATCA GAATTCCAGT 180
TCTCGAGCGC CACCCGGAGA GTTCACATTT CCCCTCCTCC GAGGCCGCGT GGTGCGCAAG 240
AAAGAGCCCG AGGGCGGCGG CAGCACACGT CTGGGCAGCC CCCTCCCCGT ACCCAGCAGC 300
GTGTACGCAG GAAAAGAAAA AGCCAAGAGA AAAACGTGGA CTGTAAAAGC CAAAACGCAG 360
AACCATCTAC TACTAACTAC CGACAACCCC AGGCGGGAGT TTGCAAGGAG TAAGCAACCC 420
TCTAATAGAA ACTACAACTA AAATAATTCC TCTCTTCGCG TTCTATTAAG GTCCTGGAAG 480
GTGGAACGCA AAGGGGACCC TGTCTTCTTA GGACACAGAC TGGCTGCGCC GATAGTGCTC 540
AGCCCCGCAC CTCCTGAGCA TACATTTAAT GTTAGGCAAA GAGCAAGTTT CCTATCTACC 600
GTTTGACCAC AGTTTCTCAC AGTATTTCTA ATTGATTCAA CGTGTATTAG ATTGAAACAA 660
AAATGATCTT GGTTGGAATA TACACGGGCA ACCTGTATTT AGATGGGGTA AGTTCCTGCA 720
GCTATCTGAC CACATTTGTC TGGTCCCTCT GAGAATCCAC GTTTTCTAGC CCGAGAAGGG 780
GCAGGCGGCC CTCATGGCGC CTCCTTCGGC GGTTTCCTGG CGAAGCGCCC ATCCTCCCCA 840
AGCACCAGGA ACGGAGGCCG TCCATATTAA TACTCGCGGG CAGCCTGTTC TGACCTATAC 900
TGTCATTTTT TCCATCGGTC GGGATCGGGC TGGGGGTGGG GTGGGGCGGG GGCTCTCCTC 960
CGAGGGGCTC AGCACGGATC GTTGGGTTTT CCCCGGCGAA CTTAACACGG AGGCAAAAGG 1020
GGCAGATGGA AACCAGGCCC CGGCTGGCCC CGCGCGCGTA AGCGCGGCAC TCAGCAGCTC 1080
GACGCAAAGC CAGGGCTGGA TTTTCGCGGC CCGGGCCCGG CGGCCGCCCA GCGCCCGCGC 1140
GATCCTCTCT CCTTCGGGTT GAGCAAACGT GGTCGCCTAA TTCCGCCCGG GAGACAGCAG 1200
CTGTGCGGCG AGAGGGGGAG AAAAAATATC GCAACTTTTC CAACAGAAAG TGTGTGCGCA 1260
CACGAGAGGT GAAGGCCCAC CCCGATTCTG TGCACGTATC GACACAGCAT CTAATCAGTG 1320
TCACTGCCAG GAATACGCTT CCGCGGCGGG CGACACCGCC GCCCTCGCCA ACCTGCAGGA 1380
GGGAGGGGGG ATGCAAATGG CGTCTCGCGT CGTCCTAGAC TCCGCGCAGC ACCCGCTACC 1440
GCGACTCCAA GCAGACGTTG CAGCAAACTG GGGTGCAGCG TCTGGGGACG CGAACGCGCA 1500
GGCGGCCCGA GCGGTCGCAG GGAAGAGGAA CTAGCACCAC TCCCCGCTAC GAGACCGTTC 1560
CCCGCCCCCA CCTCCGGAAG AGCCGCCCTT ACTCGACTGG GGTGAGGGGC GGGAAACTTT 1620
GCAAGAAGAC TGTTCCGCGC CTTCCCCGCG TGGCACCTCA GAAGAACGTG GGTGGGTTTC 1680
CCGTCCGAGG CCAGACCACG CTACCCTACT TTTCCAGGTT TCGGACCTGA ACCTCGTGGA 1740
CTACGGGAGG GAGAGTACAT TTCGGGCCAC TGCGGGGGGC GGAGGGACAC CAAAGACAGG 1800
CGTCTTCAAG GGTTCTGGCA GATGGCCAAG TTTGTGTCCT TTCCCTCCCA CGCTAGAGTA 1860
GCGCACGCCA CTTTGGGGAA GCGTGAGACC GTTCACCACC GGCCACGAGG CCACCAATGT 1920
CTTCCAGGTG GGGCCGATGG TTTGTCTGCA GCACTCCCTT CCGCCTTGCG GTCCTCGCCT 1980
GGCTCCCACA GTCCTGGGGA GCCCCCAGAG CTAGCCCGCG TCTTCCCTCG CCCGCTCTTC 2040
CGGGGGAAAG GGAGGCTGTT TGTGTGGTGT GTAGCCCCGC TCCGGCTTGC ACCCCCGCGA 2100
GCCACCTCGC AGCCCTCCCC GGCCTCGGCC TCACGGATCC CCTCCCGGAG TAGCCCCGCG 2160
GGCCCCCCCG CCATGCGTAA TGGGGCGCCC CTGGGACGCA GGCGGGGATG GCGGTTCCGG 2220
TCGTTCCGGG ATTTGCGTGC AAGAAGAAAA CAAGGCCGGC GACTACAAGA GCGGCGACTC 2280
CATTCTTGGG GTTCAGACGC CCTCGCAGCC TCCGCGTCGG TTCCGCTCTC GCCCCGGGAG 2340
CCCGCTTCCG TGTCCCTGCC CCCGCCCCCC AACGATTCCT CGTCCGGCCC GTGCCGCACC 2400
ACGCGGAGCT CCGCGCGCCC TGGCTCCCAC ACCGGTCCCT CCATAACTCG CGCTCCTCCC 2460
TCGCTCCGGG CTCGGGGAGC CGCTCGCTCC CAGCGCCCAG AGTCAGCCGG TTCCACCTTC 2520
GGCTGCGAGA GCCGCCGCCC CGCGCCACCC CCGCCCGGCC CGGCCCTTGT CCCAGCCCGG 2580
CTCCCCCGCC AGCTGCGCCG CCACCGCCGC ACGTGACCCG CCCCCGTCGC GGCTTCCGCT 2640
GAGCTGCCTG TTCCGGGGCA CAAACAATTT TTGCTCTGAC GCGGGGTCTC TCGGGGGCCC 2700
TGGCGTCCTC TACTCCCTGC TCCCCACCCC ACCCCACCCC CTACCTTCCG GGTAGGAGAA 2760
CTCAAAACAA CTCGCTGACC 2780