EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS176-43347 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chrX:40034100-40036250 
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
AGTATTTCTA ATTGATTCAA CGTGTATTAG ATTGAAACAA AAATGATCTT GGTTGGAATA 60
TACACGGGCA ACCTGTATTT AGATGGGGTA AGTTCCTGCA GCTATCTGAC CACATTTGTC 120
TGGTCCCTCT GAGAATCCAC GTTTTCTAGC CCGAGAAGGG GCAGGCGGCC CTCATGGCGC 180
CTCCTTCGGC GGTTTCCTGG CGAAGCGCCC ATCCTCCCCA AGCACCAGGA ACGGAGGCCG 240
TCCATATTAA TACTCGCGGG CAGCCTGTTC TGACCTATAC TGTCATTTTT TCCATCGGTC 300
GGGATCGGGC TGGGGGTGGG GTGGGGCGGG GGCTCTCCTC CGAGGGGCTC AGCACGGATC 360
GTTGGGTTTT CCCCGGCGAA CTTAACACGG AGGCAAAAGG GGCAGATGGA AACCAGGCCC 420
CGGCTGGCCC CGCGCGCGTA AGCGCGGCAC TCAGCAGCTC GACGCAAAGC CAGGGCTGGA 480
TTTTCGCGGC CCGGGCCCGG CGGCCGCCCA GCGCCCGCGC GATCCTCTCT CCTTCGGGTT 540
GAGCAAACGT GGTCGCCTAA TTCCGCCCGG GAGACAGCAG CTGTGCGGCG AGAGGGGGAG 600
AAAAAATATC GCAACTTTTC CAACAGAAAG TGTGTGCGCA CACGAGAGGT GAAGGCCCAC 660
CCCGATTCTG TGCACGTATC GACACAGCAT CTAATCAGTG TCACTGCCAG GAATACGCTT 720
CCGCGGCGGG CGACACCGCC GCCCTCGCCA ACCTGCAGGA GGGAGGGGGG ATGCAAATGG 780
CGTCTCGCGT CGTCCTAGAC TCCGCGCAGC ACCCGCTACC GCGACTCCAA GCAGACGTTG 840
CAGCAAACTG GGGTGCAGCG TCTGGGGACG CGAACGCGCA GGCGGCCCGA GCGGTCGCAG 900
GGAAGAGGAA CTAGCACCAC TCCCCGCTAC GAGACCGTTC CCCGCCCCCA CCTCCGGAAG 960
AGCCGCCCTT ACTCGACTGG GGTGAGGGGC GGGAAACTTT GCAAGAAGAC TGTTCCGCGC 1020
CTTCCCCGCG TGGCACCTCA GAAGAACGTG GGTGGGTTTC CCGTCCGAGG CCAGACCACG 1080
CTACCCTACT TTTCCAGGTT TCGGACCTGA ACCTCGTGGA CTACGGGAGG GAGAGTACAT 1140
TTCGGGCCAC TGCGGGGGGC GGAGGGACAC CAAAGACAGG CGTCTTCAAG GGTTCTGGCA 1200
GATGGCCAAG TTTGTGTCCT TTCCCTCCCA CGCTAGAGTA GCGCACGCCA CTTTGGGGAA 1260
GCGTGAGACC GTTCACCACC GGCCACGAGG CCACCAATGT CTTCCAGGTG GGGCCGATGG 1320
TTTGTCTGCA GCACTCCCTT CCGCCTTGCG GTCCTCGCCT GGCTCCCACA GTCCTGGGGA 1380
GCCCCCAGAG CTAGCCCGCG TCTTCCCTCG CCCGCTCTTC CGGGGGAAAG GGAGGCTGTT 1440
TGTGTGGTGT GTAGCCCCGC TCCGGCTTGC ACCCCCGCGA GCCACCTCGC AGCCCTCCCC 1500
GGCCTCGGCC TCACGGATCC CCTCCCGGAG TAGCCCCGCG GGCCCCCCCG CCATGCGTAA 1560
TGGGGCGCCC CTGGGACGCA GGCGGGGATG GCGGTTCCGG TCGTTCCGGG ATTTGCGTGC 1620
AAGAAGAAAA CAAGGCCGGC GACTACAAGA GCGGCGACTC CATTCTTGGG GTTCAGACGC 1680
CCTCGCAGCC TCCGCGTCGG TTCCGCTCTC GCCCCGGGAG CCCGCTTCCG TGTCCCTGCC 1740
CCCGCCCCCC AACGATTCCT CGTCCGGCCC GTGCCGCACC ACGCGGAGCT CCGCGCGCCC 1800
TGGCTCCCAC ACCGGTCCCT CCATAACTCG CGCTCCTCCC TCGCTCCGGG CTCGGGGAGC 1860
CGCTCGCTCC CAGCGCCCAG AGTCAGCCGG TTCCACCTTC GGCTGCGAGA GCCGCCGCCC 1920
CGCGCCACCC CCGCCCGGCC CGGCCCTTGT CCCAGCCCGG CTCCCCCGCC AGCTGCGCCG 1980
CCACCGCCGC ACGTGACCCG CCCCCGTCGC GGCTTCCGCT GAGCTGCCTG TTCCGGGGCA 2040
CAAACAATTT TTGCTCTGAC GCGGGGTCTC TCGGGGGCCC TGGCGTCCTC TACTCCCTGC 2100
TCCCCACCCC ACCCCACCCC CTACCTTCCG GGTAGGAGAA CTCAAAACAA 2150