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

TagContent
EnhancerAtlas ID
HS180-04726 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr1:226884120-226885590 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NR2C2MA0504.1chr1:226885200-226885215GGGTGTCAGAGGTCA+6.34
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_00103chr1:226883705-226886259Adipose_Nuclei
SE_03869chr1:226882978-226886945Brain_Anterior_Caudate
SE_04801chr1:226882860-226887506Brain_Cingulate_Gyrus
SE_05781chr1:226882582-226887714Brain_Hippocampus_Middle
SE_06710chr1:226882929-226887612Brain_Hippocampus_Middle_150
SE_07746chr1:226861943-226887535Brain_Inferior_Temporal_Lobe
SE_10211chr1:226883113-226887633CD19_Primary
SE_10887chr1:226873819-226893407CD20
SE_11833chr1:226884870-226885986CD3
SE_14432chr1:226885121-226886000CD4_Memory_Primary_7pool
SE_15808chr1:226885089-226885992CD4_Naive_Primary_7pool
SE_17296chr1:226856971-226887803CD4p_CD25-_CD45RAp_Naive
SE_17765chr1:226858457-226887760CD4p_CD25-_CD45ROp_Memory
SE_18263chr1:226857891-226887822CD4p_CD25-_Il17-_PMAstim_Th
SE_19160chr1:226883999-226886167CD4p_CD25-_Il17p_PMAstim_Th17
SE_20012chr1:226883215-226887069CD56
SE_21910chr1:226883715-226886974CD8_Naive_8pool
SE_22315chr1:226882979-226887479CD8_primiary
SE_25774chr1:226883181-226887670Duodenum_Smooth_Muscle
SE_26570chr1:226883956-226887261Esophagus
SE_29606chr1:226884506-226885789Fetal_Muscle
SE_40782chr1:226884801-226885783Left_Ventricle
SE_48218chr1:226884845-226887424Psoas_Muscle
SE_50140chr1:226884168-226886179Sigmoid_Colon
SE_51367chr1:226884676-226887386Skeletal_Muscle
SE_52562chr1:226884081-226886148Small_Intestine
SE_53341chr1:226884203-226886402Spleen
SE_54498chr1:226882945-226887509Stomach_Smooth_Muscle
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
chr1226884834226885233
Number: 1             
IDChromosomeStartEnd
GH01I226695chr1226883341226887082
Enhancer Sequence
CCCTGGCACG TAGATAGCAA CTTATTTTAC TATCTTGGAC ACCGGCTTCC ACTTCCGACA 60
AGGCCAAAAC TTAGAGACGA AATGGCACAT GCCCGGCCCC TGTATTTTCT ACTGTTTTCT 120
GAGAACATAA TTTCTAGTTG GAGTATTAAT TACTAGCTTG GAGCATTACT AGCTGCTGCT 180
ATTTCTCAGG GTCCCCTTGG AGACCAAGCA ACCGCTAAGA TGGCTGGCTT TCTCCATAGA 240
ACTCACAGCT AGCACCAGCA ATGAGGAAAT ACGCACACGC GCACACACAC ACACGCAGTC 300
TTTACATCTG GTTAGGGCTC CAAGTATTTC CTAAGTGTCT CATCACACTT ACTAAGGCCT 360
GAGAATCTCA GAGCTGAGAC ACTGCAGAGG TGATGTAGCC CAAGCCATCC CCTGAGGCCT 420
GAGTGTCCTC TGCAGCACCC GACTAGGGGC CGGGGGGTTA GCACAACCTG TCCCCATTCC 480
CAGGAAAAAA CCCAGCACAC AGCTCACACT CAATGATGTC AGCTTCCTAC AGGAAGGACA 540
GGTACAGCAT CACTAATTAA AAAGAGGTCA CAACCACGAA GTTCATTCAT CCAGGCCTCT 600
TGGGAACAAA TCATATCAAC AACCACCAAA CAAATGGATT CATGTTAATT TGGAGGTATT 660
CTTATCTGAG AGCAATAGAA TATAGTTCAC CAAAGCAGAA ACCTGGGCAA GCGTCAACTA 720
AATGTTGGTG GGTCCAGGAA GAAATCCACT GATTCAGGCT AGGTGCCTGT CACAACTTGG 780
TTAGCCTTTC TGAACCTGTT TCCTTGTCTG AAAGATGAAA GTAGCAATAG TTGCTGTGAG 840
GCGTGATTAA GGCATGATGC ATTCAGAGGC ATAGTACAGT GTCTGGCAAA GATTCAAGAA 900
ACTTTAGACT CTTTCCCCTT TCTGCACCAA TAAGCAAATC TGAAAAGATC ATGAATACAC 960
AGTGCTGCAA AATGAGAAAC AGAATTTCCC CCTTTAGACA AGAGAGCACT GTGATGCAGA 1020
CACAGCCCTG GCATCAGCAA GGAAGGCCCT GGTTCCCCTT CTCATCATCC CTGGAGAGAT 1080
GGGTGTCAGA GGTCAGGTGA GGGAATCTCT TTGTGCGTGA TTCTCCAACT CTGCAAACAA 1140
TAGCTGGCCA TTTCTTCTGA GGAATAAGCT GAAATCAAAC ATACCTGATA GGCGAACTGG 1200
GCTTGATGCA GTCCCAAGCA CTCTGCTGAG CACTGAAGCC ACTTTTCCTC ACCACAACTA 1260
TGGGAGCTAG AGAAGGGAGG CGATTAGTGG TGAAGACAGT GGGGACCTGC CCCAGGTGGC 1320
ATTAGTGAAA TAGACAATTC TCTAGGGTCC TCTGCACCAA CCCAGAACTC TCCACATAAG 1380
AGCTGCCCTA GGAACACCAC AGTTCTGTGG CCTGCCCTGG CAGATGTGCC CTCACATCTG 1440
GGTGATAAGG GGTCCCCAAG AGGAGCCAAA 1470