EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS133-03715 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr1:226895260-226898030 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
PLAG1MA0163.1chr1:226895301-226895315GGGGCTCAATGGGG+6.22
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_00103chr1:226895483-226898785Adipose_Nuclei
SE_03159chr1:226896014-226897655Brain_Angular_Gyrus
SE_03869chr1:226895318-226903205Brain_Anterior_Caudate
SE_04801chr1:226895006-226903563Brain_Cingulate_Gyrus
SE_05781chr1:226895547-226902956Brain_Hippocampus_Middle
SE_06710chr1:226895689-226902924Brain_Hippocampus_Middle_150
SE_07746chr1:226895520-226903147Brain_Inferior_Temporal_Lobe
SE_10887chr1:226895020-226908737CD20
SE_11833chr1:226897235-226900945CD3
SE_13607chr1:226896344-226898855CD34_Primary_RO01536
SE_15808chr1:226897023-226899338CD4_Naive_Primary_7pool
SE_17296chr1:226887872-226908646CD4p_CD25-_CD45RAp_Naive
SE_17765chr1:226895238-226903199CD4p_CD25-_CD45ROp_Memory
SE_18263chr1:226887975-226903974CD4p_CD25-_Il17-_PMAstim_Th
SE_19160chr1:226895672-226897237CD4p_CD25-_Il17p_PMAstim_Th17
SE_20012chr1:226895917-226897123CD56
SE_20012chr1:226897222-226902648CD56
SE_21455chr1:226895829-226902101CD8_Naive_7pool
SE_21910chr1:226895551-226902316CD8_Naive_8pool
SE_22315chr1:226895328-226903225CD8_primiary
SE_25774chr1:226895022-226903030Duodenum_Smooth_Muscle
SE_26570chr1:226895901-226897946Esophagus
SE_29606chr1:226896130-226897123Fetal_Muscle
SE_40782chr1:226895952-226898958Left_Ventricle
SE_42228chr1:226895968-226897926Lung
SE_48218chr1:226895940-226897776Psoas_Muscle
SE_48643chr1:226895972-226897788Right_Atrium
SE_50140chr1:226896002-226901571Sigmoid_Colon
SE_51367chr1:226895995-226897348Skeletal_Muscle
SE_52562chr1:226895907-226897800Small_Intestine
SE_53341chr1:226896682-226897424Spleen
SE_54498chr1:226895554-226900516Stomach_Smooth_Muscle
SE_55112chr1:226897244-226897811Thymus
SE_58303chr1:226819953-226937809Ly1
SE_59629chr1:226819233-226928465Ly4
SE_60416chr1:226819368-226929640DHL6
SE_61009chr1:226812849-226900772HBL1
SE_62233chr1:226813614-226929647Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1226896121226896509
Number: 2             
IDChromosomeStartEnd
GH01I226705chr1226892964226895310
GH01I226708chr1226896014226902612
Enhancer Sequence
CAGCTTACTA TATAAAATGC CATCAACATG TTCGGGCAGT GGGGGCTCAA TGGGGATAAA 60
TAGGCAGTGT ACACATGAGT AACTCAAGGC CATCATCACA AGGAAACATG TAGAGTCCCT 120
CTTGAAAACT AAAGAATTAC AAATTACAAC TTCAAGGGAC AGTAAGACAA TATCAAACTA 180
CAAACAAAAT CCAATGGTCG TAGGGAAACT GCAGCACTTA GACTTTACAG ATGACCCCGT 240
AATTGGCTCA GTCTTTCCAG AGAGTAGTGT AGGAAGATGA AATATGCTAT ACATCATTCT 300
TGGTATTGGA CGTTGCCCCA GCAGTACCAC TGAGGGGAAC ACTTCCCAAG AAGTCACTAA 360
AGGGAGAAGA AAAGAGGTCA TTTTAACAAA AATACTCATG GCTGCATATG GCAATAACTG 420
CAACAAAATA TGGAAACTAC CCACCAAAGG TAGGAGTAAG ATGATGTAAA TGATGTAGTA 480
GCTCAAAGTT CACACTCAGG AATCAGACCA CACAGTTGAT TACTGTATGA AATGACGTTA 540
AAACAATAAA AGATAAAACT AGTACAATCA GATTGCAATT ATGTAAAACA AAATTAGGCA 600
ATTGATCAAA GACCAAATTG GATTTACAAC GATTGTAAAT ACCTAGAATG AGTTAAATCA 660
TTCATTTAGT CGTGGTTATC ATTATTTAGT CATGGTTATC ATTAGCTTCT TTCTCTGTAA 720
TGTTTAAGTT TTTGTTAAAA ACCAAAAAGA ACAAAAAATA AATCAAACCT GCCTCAAACC 780
GTTGGTAGAA TAACAGCTCA AGGGACCTAA CTGAGACCCA CCCAAATGTA TGCTCTTTGG 840
AGCTACTCCC AGAGTCAATA CTAATTGTTA TAAGCCACTC CCATGCCAGA GGCTGACTTA 900
GGCACGAGTA ACTCGAGACA TTCTGGTCAA TGAGACACAG GGGATATCTG CTGGGAGCCT 960
TCTGAAAAAG ATGTCTCGGC CTTAGACACC ATGAAGAGCC ATCCCCTTTT TCCTCCAAGG 1020
GATATTATCA TTTCCACACA GGACACGAGG CCCTGTAGCA CCCATCTGGC AACCACGAGG 1080
AAAGATGAGT CAACACGTTG TGAGACAGGG CAGAGAGATG CAGAGGACAC AGGTCTTTCA 1140
GTAACTCTGC TATGCTGATG AATTAGCCAA TGCTAGAACT GCCTGTGCTG GGACTTACTG 1200
ATCAAGGTGA AAGAATGTGT TTTCTTTATT GTTCAACTCT ACTGGGTTGC AGTTTTCTGA 1260
TACTTGCAGC TGACAGCATC TTAACTCGTG AGGCAGCAAG CCTGAGCAGC TTTCTGATGC 1320
AGGCCTGGCA GGCCATGCTG CCCTAGGCCA GTATTCTGCC AGGCCCCTCA CTGTATTCCA 1380
TTCTGGGGGA GAGCCTAAGG GAGACGGAAG AAGACACTGG TGAACACGAG TTACACCAGG 1440
CCTCAGAACA ACTCCAGATG GTACAGCAAG CAGGTGGCAG CAGTGGGCAG CAGAGCCCCA 1500
GACGTCTGGC CCCTCAATAG GGGACCTCCA GAGGCCTCTG GGCCACCAGC TGTCTCCTTT 1560
CTGGATTCAC CCATTTCACA AAGGCTGTGA CAAAACTGCC TTCTGGGTTA GAGCTGCCAG 1620
AAAAAGTACA GGATGCCCAG TTACGTTTGG ATTTTAGATA AACAACAAGT GACTTTTTAG 1680
CATGAGTATG TCTCATGCCT TTATTCTGGC TGCACCCCCT CCCTGGCGAG GCACCAGGCT 1740
AGCAACATCC AGAAACAGAG ATGGCCTCCC CTGCCCTGGG CTGCCTGTCT GGGCTGCCGT 1800
GGGTGTGTCT GGCCCAGTGG TAGGAGGATG TCCAGTGTCT GGCCTCTCCA GGTCTCCGAT 1860
GGGTCTAGGA ATGTCTGATG TGCATTTTAT AGTAACAGAC AAGAAGTGGC TAACACTTAA 1920
AATGTATGGG TGGGGTGGGT GTCACTGCGG TCCTGGGACA CTTGGAAACT ATGCAGCAGG 1980
CTGTGGAGGG GACTAGGGTA GAGGCAGGCA CAGTGGCTCC TGACATCCAA CTTCCCCCCA 2040
ACAAGAACTT CCTAGGTAAA GCAGAAGACG TGATACTTCC CTGACCTTCC TTTGTCTAAA 2100
TATGAAACTT CCATGACTGG GGACCAACGG TGAGAAGCGG CAGTGGGCAG GGCCTAGCCC 2160
TCACCTGTCC CTGTCTACAG GCCCACCTGA CCTGCAATTA GGTTTCCTCA CTGTCATTCT 2220
CTCTTGGGCC ATGTCTTACG GCATGATACT CCTGCCCAAG GACAGTGCTT AACTTGTTTG 2280
GTGCAGCACT ATCTCCCTGC TTGAAGAGAG TCCCTTAGTA AAGCTTGCTG ATGAGAGCAG 2340
AGCCTCATTT CTTGCAACCT TGCTTTATGG TTCCCTGTCT AGTATCCTGA CAGCATCCTG 2400
CCTGGGGCCA GCACTAGCTC ATAACTACCT GGGAAGAAAT CACTCCCTAA TGGGAAGATT 2460
CACAACCCAC CCACCACAAA ATTCAGCCAC ATCCCAGTGA CAGATAAATC TGTCTTCCCT 2520
GCCCCTGTCT CCTCTCCCCT GACTCACGGC CTCCTTCAGA AGGTGCCGTG CTAACAGGTA 2580
GCATTGGAAA AGAAGTCTGG GGTGGGGCAG CTGGTGATTG GCTGGTGATA ATGTCCCTCA 2640
GAAGAACAGA AAGGGGGAAA CAAATGGAAG CACCTGTGTT CATGGTGAGC CCTTTTAACT 2700
AGTTATTTCT TTTTAGAAAC GGGAGACAGA AAATAAACAG AAACTGCAGA TAGCAATGAA 2760
GTAAGCAAGT 2770